Molecular basis of reproductive senescence: insights from model organisms.
Aging
Cohesion
DNA damage
Nondisjunction
Oocyte quality
Proteostasis
Journal
Journal of assisted reproduction and genetics
ISSN: 1573-7330
Titre abrégé: J Assist Reprod Genet
Pays: Netherlands
ID NLM: 9206495
Informations de publication
Date de publication:
Jan 2021
Jan 2021
Historique:
received:
17
08
2020
accepted:
25
09
2020
pubmed:
3
10
2020
medline:
2
7
2021
entrez:
2
10
2020
Statut:
ppublish
Résumé
Reproductive decline due to parental age has become a major barrier to fertility as couples have delayed having offspring into their thirties and forties. Advanced parental age is also associated with increased incidence of neurological and cardiovascular disease in offspring. Thus, elucidating the etiology of reproductive decline is of clinical importance. Deciphering the underlying processes that drive reproductive decline is particularly challenging in women in whom a discrete oocyte pool is established during embryogenesis and may remain dormant for tens of years. Instead, our understanding of the processes that drive reproductive senescence has emerged from studies in model organisms, both vertebrate and invertebrate, that are the focus of this literature review. Studies of reproductive aging in model organisms not only have revealed the detrimental cellular changes that occur with age but also are helping identify major regulator proteins controlling them. Here, we discuss what we have learned from model organisms with respect to the molecular mechanisms that maintain both genome integrity and oocyte quality.
Identifiants
pubmed: 33006069
doi: 10.1007/s10815-020-01959-4
pii: 10.1007/s10815-020-01959-4
pmc: PMC7822982
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
17-32Subventions
Organisme : NIA NIH HHS
ID : R56 AG066682
Pays : United States
Organisme : National Institute of General Medical Sciences (US)
ID : R01GM104007
Organisme : NIA NIH HHS
ID : R01 AG051659
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM104007
Pays : United States
Organisme : National Institute on Aging (US)
ID : R01AG051659
Références
Roeters van Lennep JE, Heida KY, Bots ML, Hoek A, collaborators of the Dutch Multidisciplinary Guideline Development Group on Cardiovascular Risk Management after Reproductive D. Cardiovascular disease risk in women with premature ovarian insufficiency: a systematic review and meta-analysis. Eur J Prev Cardiol. 2016;23(2):178–86. https://doi.org/10.1177/2047487314556004 .
doi: 10.1177/2047487314556004
pubmed: 25331207
Hughes SE, Evason K, Xiong C, Kornfeld K. Genetic and pharmacological factors that influence reproductive aging in nematodes. PLoS Genet. 2007;3(2):e25. https://doi.org/10.1371/journal.pgen.0030025 .
doi: 10.1371/journal.pgen.0030025
pubmed: 17305431
pmcid: 1797816
Luo S, Kleemann GA, Ashraf JM, Shaw WM, Murphy CT. TGF-β and insulin signaling regulate reproductive aging via oocyte and germline quality maintenance. Cell. 2010;143(2):299–312. https://doi.org/10.1016/j.cell.2010.09.013 .
doi: 10.1016/j.cell.2010.09.013
pubmed: 20946987
pmcid: 2955983
Fuchs E, Tumbar T, Guasch G. Socializing with the neighbors: stem cells and their niche. Cell. 2004;116(6):769–78. https://doi.org/10.1016/s0092-8674(04)00255-7 .
doi: 10.1016/s0092-8674(04)00255-7
pubmed: 15035980
Ward EJ, Shcherbata HR, Reynolds SH, Fischer KA, Hatfield SD, Ruohola-Baker H. Stem cells signal to the niche through the Notch pathway in the Drosophila ovary. Curr Biol. 2006;16(23):2352–8. https://doi.org/10.1016/j.cub.2006.10.022 .
doi: 10.1016/j.cub.2006.10.022
pubmed: 17070683
Zhao R, Xuan Y, Li X, Xi R. Age-related changes of germline stem cell activity, niche signaling activity and egg production in Drosophila. Aging Cell. 2008;7(3):344–54. https://doi.org/10.1111/j.1474-9726.2008.00379.x .
doi: 10.1111/j.1474-9726.2008.00379.x
pubmed: 18267001
Pan L, Chen S, Weng C, Call G, Zhu D, Tang H, et al. Stem cell aging is controlled both intrinsically and extrinsically in the Drosophila ovary. Cell Stem Cell. 2007;1(4):458–69. https://doi.org/10.1016/j.stem.2007.09.010 .
doi: 10.1016/j.stem.2007.09.010
pubmed: 18371381
Kao SH, Tseng CY, Wan CL, Su YH, Hsieh CC, Pi H, et al. Aging and insulin signaling differentially control normal and tumorous germline stem cells. Aging Cell. 2015;14(1):25–34. https://doi.org/10.1111/acel.12288 .
doi: 10.1111/acel.12288
pubmed: 25470527
Sato E, Kimura N, Yokoo M, Miyake Y, Ikeda JE. Morphodynamics of ovarian follicles during oogenesis in mice. Microsc Res Tech. 2006;69(6):427–35. https://doi.org/10.1002/jemt.20302 .
doi: 10.1002/jemt.20302
pubmed: 16718657
Silver LM. Mouse genetics : concepts and applications. New York: Oxford University Press; 1995.
Garigan D, Hsu AL, Fraser AG, Kamath RS, Ahringer J, Kenyon C. Genetic analysis of tissue aging in Caenorhabditis elegans: a role for heat-shock factor and bacterial proliferation. Genetics. 2002;161(3):1101–12.
pubmed: 12136014
pmcid: 1462187
Killian DJ, Hubbard EJ. Caenorhabditis elegans germline patterning requires coordinated development of the somatic gonadal sheath and the germ line. Dev Biol. 2005;279(2):322–35. https://doi.org/10.1016/j.ydbio.2004.12.021 .
doi: 10.1016/j.ydbio.2004.12.021
pubmed: 15733661
Kocsisova Z, Kornfeld K, Schedl T. Rapid population-wide declines in stem cell number and activity during reproductive aging in C. elegans. Development. 2019;146(8). https://doi.org/10.1242/dev.173195 .
Narbonne P, Maddox PS, Labbe JC. DAF-18/PTEN locally antagonizes insulin signalling to couple germline stem cell proliferation to oocyte needs in C. elegans. Development. 2015;142(24):4230–41. https://doi.org/10.1242/dev.130252 .
doi: 10.1242/dev.130252
pubmed: 26552888
pmcid: 6514392
Qin Z, Hubbard EJ. Non-autonomous DAF-16/FOXO activity antagonizes age-related loss of C. elegans germline stem/progenitor cells. Nat Commun. 2015;6:7107. https://doi.org/10.1038/ncomms8107 .
doi: 10.1038/ncomms8107
pubmed: 25960195
pmcid: 4432587
Shi C, Murphy CT. Mating induces shrinking and death in Caenorhabditis mothers. Science. 2014;343(6170):536–40. https://doi.org/10.1126/science.1242958 .
doi: 10.1126/science.1242958
pubmed: 24356112
Hubbard EJA, Schedl T. Biology of the Caenorhabditis elegans germline stem cell system. Genetics. 2019;213(4):1145–88. https://doi.org/10.1534/genetics.119.300238 .
doi: 10.1534/genetics.119.300238
pubmed: 31796552
pmcid: 6893382
Gordon KL, Payne SG, Linden-High LM, Pani AM, Goldstein B, Hubbard EJA, et al. Ectopic germ cells can induce niche-like enwrapment by neighboring body wall muscle. Curr Biol. 2019;29(5):823–33 e5. https://doi.org/10.1016/j.cub.2019.01.056 .
doi: 10.1016/j.cub.2019.01.056
pubmed: 30799241
pmcid: 6457669
Starich TA, Hall DH, Greenstein D. Two classes of gap junction channels mediate soma-germline interactions essential for germline proliferation and gametogenesis in Caenorhabditis elegans. Genetics. 2014;198(3):1127–53. https://doi.org/10.1534/genetics.114.168815 .
doi: 10.1534/genetics.114.168815
pubmed: 25195067
pmcid: 4224157
Byrd DT, Knobel K, Affeldt K, Crittenden SL, Kimble J. A DTC niche plexus surrounds the germline stem cell pool in Caenorhabditis elegans. PLoS One. 2014;9(2):e88372. https://doi.org/10.1371/journal.pone.0088372 .
doi: 10.1371/journal.pone.0088372
pubmed: 24586318
pmcid: 3929564
Xie T, Spradling AC. decapentaplegic is essential for the maintenance and division of germline stem cells in the Drosophila ovary. Cell. 1998;94(2):251–60. https://doi.org/10.1016/s0092-8674(00)81424-5 .
doi: 10.1016/s0092-8674(00)81424-5
pubmed: 9695953
Drummond-Barbosa D. Local and physiological control of germline stem cell lineages in Drosophila melanogaster. Genetics. 2019;213(1):9–26. https://doi.org/10.1534/genetics.119.300234 .
doi: 10.1534/genetics.119.300234
pubmed: 31488592
pmcid: 6727809
Wallenfang MR, Nayak R, DiNardo S. Dynamics of the male germline stem cell population during aging of Drosophila melanogaster. Aging Cell. 2006;5(4):297–304. https://doi.org/10.1111/j.1474-9726.2006.00221.x .
doi: 10.1111/j.1474-9726.2006.00221.x
pubmed: 16800845
Harrison DA, McCoon PE, Binari R, Gilman M, Perrimon N. Drosophila unpaired encodes a secreted protein that activates the JAK signaling pathway. Genes Dev. 1998;12(20):3252–63. https://doi.org/10.1101/gad.12.20.3252 .
doi: 10.1101/gad.12.20.3252
pubmed: 9784499
pmcid: 317220
Kiger AA, Jones DL, Schulz C, Rogers MB, Fuller MT. Stem cell self-renewal specified by JAK-STAT activation in response to a support cell cue. Science. 2001;294(5551):2542–5. https://doi.org/10.1126/science.1066707 .
doi: 10.1126/science.1066707
pubmed: 11752574
Tulina N, Matunis E. Control of stem cell self-renewal in Drosophila spermatogenesis by JAK-STAT signaling. Science. 2001;294(5551):2546–9. https://doi.org/10.1126/science.1066700 .
doi: 10.1126/science.1066700
pubmed: 11752575
Boyle M, Wong C, Rocha M, Jones DL. Decline in self-renewal factors contributes to aging of the stem cell niche in the Drosophila testis. Cell Stem Cell. 2007;1(4):470–8. https://doi.org/10.1016/j.stem.2007.08.002 .
doi: 10.1016/j.stem.2007.08.002
pubmed: 18371382
Toledano H, D'Alterio C, Czech B, Levine E, Jones DL. The let-7-Imp axis regulates ageing of the Drosophila testis stem-cell niche. Nature. 2012;485(7400):605–10. https://doi.org/10.1038/nature11061 .
doi: 10.1038/nature11061
pubmed: 22660319
pmcid: 4829122
Epstein Y, Perry N, Volin M, Zohar-Fux M, Braun R, Porat-Kuperstein L, et al. miR-9a modulates maintenance and ageing of Drosophila germline stem cells by limiting N-cadherin expression. Nat Commun. 2017;8(1):600. https://doi.org/10.1038/s41467-017-00485-9 .
doi: 10.1038/s41467-017-00485-9
pubmed: 28928361
pmcid: 5605507
Zhang M, Chambers I. Segregation of the mouse germline and soma. Cell Cycle. 2019;18(22):3064–71. https://doi.org/10.1080/15384101.2019.1672466 .
doi: 10.1080/15384101.2019.1672466
pubmed: 31583942
pmcid: 6816410
Vincent SD, Dunn NR, Sciammas R, Shapiro-Shalef M, Davis MM, Calame K, et al. The zinc finger transcriptional repressor Blimp1/Prdm1 is dispensable for early axis formation but is required for specification of primordial germ cells in the mouse. Development. 2005;132(6):1315–25. https://doi.org/10.1242/dev.01711 .
doi: 10.1242/dev.01711
pubmed: 15750184
Ohinata Y, Payer B, O'Carroll D, Ancelin K, Ono Y, Sano M, et al. Blimp1 is a critical determinant of the germ cell lineage in mice. Nature. 2005;436(7048):207–13. https://doi.org/10.1038/nature03813 .
doi: 10.1038/nature03813
pubmed: 15937476
Tanaka SS, Toyooka Y, Akasu R, Katoh-Fukui Y, Nakahara Y, Suzuki R, et al. The mouse homolog of Drosophila Vasa is required for the development of male germ cells. Genes Dev. 2000;14(7):841–53.
pubmed: 10766740
pmcid: 316497
Wei Y, Reveal B, Reich J, Laursen WJ, Senger S, Akbar T, et al. TORC1 regulators Iml1/GATOR1 and GATOR2 control meiotic entry and oocyte development in Drosophila. Proc Natl Acad Sci U S A. 2014;111(52):E5670–7. https://doi.org/10.1073/pnas.1419156112 .
doi: 10.1073/pnas.1419156112
pubmed: 25512509
pmcid: 4284557
Gumienny TL, Lambie E, Hartwieg E, Horvitz HR, Hengartner MO. Genetic control of programmed cell death in the Caenorhabditis elegans hermaphrodite germline. Development. 1999;126(5):1011–22.
pubmed: 9927601
Andux S, Ellis RE. Apoptosis maintains oocyte quality in aging Caenorhabditis elegans females. PLoS Genet. 2008;4(12):e1000295. https://doi.org/10.1371/journal.pgen.1000295 .
doi: 10.1371/journal.pgen.1000295
pubmed: 19057674
pmcid: 2585808
Perez GI, Robles R, Knudson CM, Flaws JA, Korsmeyer SJ, Tilly JL. Prolongation of ovarian lifespan into advanced chronological age by Bax-deficiency. Nat Genet. 1999;21(2):200–3. https://doi.org/10.1038/5985 .
doi: 10.1038/5985
pubmed: 9988273
Chu HP, Liao Y, Novak JS, Hu Z, Merkin JJ, Shymkiv Y, et al. Germline quality control: eEF2K stands guard to eliminate defective oocytes. Dev Cell. 2014;28(5):561–72. https://doi.org/10.1016/j.devcel.2014.01.027 .
doi: 10.1016/j.devcel.2014.01.027
pubmed: 24582807
pmcid: 4712648
Bolcun-Filas E, Rinaldi VD, White ME, Schimenti JC. Reversal of female infertility by Chk2 ablation reveals the oocyte DNA damage checkpoint pathway. Science. 2014;343(6170):533–6. https://doi.org/10.1126/science.1247671 .
doi: 10.1126/science.1247671
pubmed: 24482479
pmcid: 4048839
Malki S, van der Heijden GW, O'Donnell KA, Martin SL, Bortvin A. A role for retrotransposon LINE-1 in fetal oocyte attrition in mice. Dev Cell. 2014;29(5):521–33. https://doi.org/10.1016/j.devcel.2014.04.027 .
doi: 10.1016/j.devcel.2014.04.027
pubmed: 24882376
pmcid: 4056315
Drummond-Barbosa D, Spradling AC. Stem cells and their progeny respond to nutritional changes during Drosophila oogenesis. Dev Biol. 2001;231(1):265–78. https://doi.org/10.1006/dbio.2000.0135 .
doi: 10.1006/dbio.2000.0135
pubmed: 11180967
Hsu HJ, Drummond-Barbosa D. Insulin levels control female germline stem cell maintenance via the niche in Drosophila. Proc Natl Acad Sci U S A. 2009;106(4):1117–21. https://doi.org/10.1073/pnas.0809144106 .
doi: 10.1073/pnas.0809144106
pubmed: 19136634
pmcid: 2633547
McLeod CJ, Wang L, Wong C, Jones DL. Stem cell dynamics in response to nutrient availability. Curr Biol. 2010;20(23):2100–5. https://doi.org/10.1016/j.cub.2010.10.038 .
doi: 10.1016/j.cub.2010.10.038
pubmed: 21055942
pmcid: 3005562
Yang H, Yamashita YM. The regulated elimination of transit-amplifying cells preserves tissue homeostasis during protein starvation in Drosophila testis. Development. 2015;142(10):1756–66. https://doi.org/10.1242/dev.122663 .
doi: 10.1242/dev.122663
pubmed: 25968311
pmcid: 4440929
Mair W, McLeod CJ, Wang L, Jones DL. Dietary restriction enhances germline stem cell maintenance. Aging Cell. 2010;9(5):916–8. https://doi.org/10.1111/j.1474-9726.2010.00602.x .
doi: 10.1111/j.1474-9726.2010.00602.x
pubmed: 20569233
pmcid: 2944899
Blackwell TK, Sewell AK, Wu Z, Han M. TOR signaling in Caenorhabditis elegans development, metabolism, and aging. Genetics. 2019;213(2):329–60. https://doi.org/10.1534/genetics.119.302504 .
doi: 10.1534/genetics.119.302504
pubmed: 31594908
pmcid: 6781902
Korta DZ, Tuck S, Hubbard EJ. S6K links cell fate, cell cycle and nutrient response in C. elegans germline stem/progenitor cells. Development. 2012;139(5):859–70. https://doi.org/10.1242/dev.074047 .
doi: 10.1242/dev.074047
pubmed: 22278922
pmcid: 3274352
Michaelson D, Korta DZ, Capua Y, Hubbard EJ. Insulin signaling promotes germline proliferation in C. elegans. Development. 2010;137(4):671–80. https://doi.org/10.1242/dev.042523 .
doi: 10.1242/dev.042523
pubmed: 20110332
pmcid: 2827619
Pinkston JM, Garigan D, Hansen M, Kenyon C. Mutations that increase the life span of C. elegans inhibit tumor growth. Science. 2006;313(5789):971–5. https://doi.org/10.1126/science.1121908 .
doi: 10.1126/science.1121908
pubmed: 16917064
Roy D, Kahler DJ, Yun C, Hubbard EJA. Functional interactions between rsks-1/S6K, glp-1/Notch, and regulators of Caenorhabditis elegans fertility and germline stem cell maintenance. G3 (Bethesda). 2018;8(10):3293–309. https://doi.org/10.1534/g3.118.200511 .
doi: 10.1534/g3.118.200511
Roy D, Michaelson D, Hochman T, Santella A, Bao Z, Goldberg JD, et al. Cell cycle features of C. elegans germline stem/progenitor cells vary temporally and spatially. Dev Biol. 2016;409(1):261–71. https://doi.org/10.1016/j.ydbio.2015.10.031 .
doi: 10.1016/j.ydbio.2015.10.031
pubmed: 26577869
Hsu HJ, Drummond-Barbosa D. Insulin signals control the competence of the Drosophila female germline stem cell niche to respond to Notch ligands. Dev Biol. 2011;350(2):290–300. https://doi.org/10.1016/j.ydbio.2010.11.032 .
doi: 10.1016/j.ydbio.2010.11.032
pubmed: 21145317
LaFever L, Feoktistov A, Hsu HJ, Drummond-Barbosa D. Specific roles of Target of rapamycin in the control of stem cells and their progeny in the Drosophila ovary. Development. 2010;137(13):2117–26. https://doi.org/10.1242/dev.050351 .
doi: 10.1242/dev.050351
pubmed: 20504961
pmcid: 2882131
Laws KM, Drummond-Barbosa D. AMP-activated protein kinase has diet-dependent and -independent roles in Drosophila oogenesis. Dev Biol. 2016;420(1):90–9. https://doi.org/10.1016/j.ydbio.2016.10.006 .
doi: 10.1016/j.ydbio.2016.10.006
pubmed: 27729213
pmcid: 5124390
Laws KM, Sampson LL, Drummond-Barbosa D. Insulin-independent role of adiponectin receptor signaling in Drosophila germline stem cell maintenance. Dev Biol. 2015;399(2):226–36. https://doi.org/10.1016/j.ydbio.2014.12.033 .
doi: 10.1016/j.ydbio.2014.12.033
pubmed: 25576925
pmcid: 4866495
Roth TM, Chiang CY, Inaba M, Yuan H, Salzmann V, Roth CE, et al. Centrosome misorientation mediates slowing of the cell cycle under limited nutrient conditions in Drosophila male germline stem cells. Mol Biol Cell. 2012;23(8):1524–32. https://doi.org/10.1091/mbc.E11-12-0999 .
doi: 10.1091/mbc.E11-12-0999
pubmed: 22357619
pmcid: 3327310
Ueishi S, Shimizu H. Y HI. Male germline stem cell division and spermatocyte growth require insulin signaling in Drosophila. Cell Struct Funct. 2009;34(1):61–9. https://doi.org/10.1247/csf.08042 .
doi: 10.1247/csf.08042
pubmed: 19384053
Wei Y, Reveal B, Cai W, Lilly MA. The GATOR1 complex regulates metabolic homeostasis and the response to nutrient stress in Drosophila melanogaster. G3 (Bethesda). 2016;6(12):3859–67. https://doi.org/10.1534/g3.116.035337 .
doi: 10.1534/g3.116.035337
Luo S, Shaw WM, Ashraf J, Murphy CT. TGF-beta Sma/Mab signaling mutations uncouple reproductive aging from somatic aging. PLoS Genet. 2009;5(12):e1000789. https://doi.org/10.1371/journal.pgen.1000789 .
doi: 10.1371/journal.pgen.1000789
pubmed: 20041217
pmcid: 2791159
Templeman NM, Cota V, Keyes W, Kaletsky R, Murphy CT. CREB non-autonomously controls reproductive aging through hedgehog/patched signaling. Dev Cell. 2020;54(1):92–105 e5. https://doi.org/10.1016/j.devcel.2020.05.023 .
doi: 10.1016/j.devcel.2020.05.023
pubmed: 32544391
Belli M, Shimasaki S. Molecular aspects and clinical relevance of GDF9 and BMP15 in ovarian function. Vitam Horm. 2018;107:317–48. https://doi.org/10.1016/bs.vh.2017.12.003 .
doi: 10.1016/bs.vh.2017.12.003
pubmed: 29544636
pmcid: 6309678
Bertoldo MJ, Faure M, Dupont J, Froment P. AMPK: a master energy regulator for gonadal function. Front Neurosci. 2015;9:235. https://doi.org/10.3389/fnins.2015.00235 .
doi: 10.3389/fnins.2015.00235
pubmed: 26236179
pmcid: 4500899
Dupont J, Scaramuzzi RJ. Insulin signalling and glucose transport in the ovary and ovarian function during the ovarian cycle. Biochem J. 2016;473(11):1483–501. https://doi.org/10.1042/BCJ20160124 .
doi: 10.1042/BCJ20160124
pubmed: 27234585
pmcid: 4888492
Guo R, Reinhardt K. Dietary polyunsaturated fatty acids affect volume and metabolism of Drosophila melanogaster sperm. J Evol Biol. 2020. https://doi.org/10.1111/jeb.13591 .
Wang X, Zhang L, Zhang L, Wang W, Wei S, Wang J, et al. Effects of excess sugars and lipids on the growth and development of Caenorhabditis elegans. Genes Nutr. 2020;15:1. https://doi.org/10.1186/s12263-020-0659-1 .
doi: 10.1186/s12263-020-0659-1
pubmed: 32015763
pmcid: 6988283
Selesniemi K, Lee H-J, Muhlhauser A, Tilly JL. Prevention of maternal aging-associated oocyte aneuploidy and meiotic spindle defects in mice by dietary and genetic strategies. Proceedings of the National Academy of Sciences. 2011.
Schultz J, Redfield H. Interchromosomal effects on crossing over in Drosophila. Cold Spring Harb Symp Quant Biol. 1951;16:175–97. https://doi.org/10.1101/sqb.1951.016.01.015 .
doi: 10.1101/sqb.1951.016.01.015
pubmed: 14942738
Stern C. An effect of temperature and age on crossing-over in the first chromosome of Drosophila melanogaster. Proc Natl Acad Sci U S A. 1926;12(8):530–2. https://doi.org/10.1073/pnas.12.8.530 .
doi: 10.1073/pnas.12.8.530
pubmed: 16587124
pmcid: 1084661
Lenz W. The effect of parental age and the number of births on congenital pathological conditions in the child. II. Acta Genet Stat Med. 1959;9:249–83.
pubmed: 14415748
Lim JG, Stine RR, Yanowitz JL. Domain-specific regulation of recombination in Caenorhabditis elegans in response to temperature, age and sex. Genetics. 2008;180(2):715–26. https://doi.org/10.1534/genetics.108.090142 .
doi: 10.1534/genetics.108.090142
pubmed: 18780748
pmcid: 2567375
Rose AM, Baillie DL. The effect of temperature and parental age on recombination and nondisjunction in Caenorhabditis elegans. Genetics. 1979;92(2):409–18.
pubmed: 17248928
pmcid: 1213967
Wood AJ, Severson AF, Meyer BJ. Condensin and cohesin complexity: the expanding repertoire of functions. Nat Rev Genet. 2010;11(6):391–404. https://doi.org/10.1038/nrg2794 .
doi: 10.1038/nrg2794
pubmed: 20442714
pmcid: 3491780
Cheng JM, Li J, Tang JX, Hao XX, Wang ZP, Sun TC, et al. Merotelic kinetochore attachment in oocyte meiosis II causes sister chromatids segregation errors in aged mice. Cell Cycle. 2017;16(15):1404–13. https://doi.org/10.1080/15384101.2017.1327488 .
doi: 10.1080/15384101.2017.1327488
pubmed: 28590163
pmcid: 5553406
Traut H. X-chromosomal nondisjunction induced by aging oocytes of Drosophila melanogaster: the special susceptibility of mature eggs. Can J Genet Cytol. 1980;22(3):433–7. https://doi.org/10.1139/g80-054 .
doi: 10.1139/g80-054
pubmed: 6778596
Jeffreys CA, Burrage PS, Bickel SE. A model system for increased meiotic nondisjunction in older oocytes. Curr Biol. 2003;13(6):498–503. https://doi.org/10.1016/s0960-9822(03)00134-9 .
doi: 10.1016/s0960-9822(03)00134-9
pubmed: 12646133
Hall H, Hunt P, Hassold T. Meiosis and sex chromosome aneuploidy: how meiotic errors cause aneuploidy; how aneuploidy causes meiotic errors. Curr Opin Genet Dev. 2006;16(3):323–9. https://doi.org/10.1016/j.gde.2006.04.011 .
doi: 10.1016/j.gde.2006.04.011
pubmed: 16647844
Hodges CA, Revenkova E, Jessberger R, Hassold TJ, Hunt PA. SMC1beta-deficient female mice provide evidence that cohesins are a missing link in age-related nondisjunction. Nat Genet. 2005;37(12):1351–5. https://doi.org/10.1038/ng1672 .
doi: 10.1038/ng1672
pubmed: 16258540
Subramanian VV, Bickel SE. Aging predisposes oocytes to meiotic nondisjunction when the cohesin subunit SMC1 is reduced. PLoS Genet. 2008;4(11):e1000263. https://doi.org/10.1371/journal.pgen.1000263 .
doi: 10.1371/journal.pgen.1000263
pubmed: 19008956
pmcid: 2577922
Khetani RS, Bickel SE. Regulation of meiotic cohesion and chromosome core morphogenesis during pachytene in Drosophila oocytes. J Cell Sci. 2007;120(Pt 17):3123–37. https://doi.org/10.1242/jcs.009977 .
doi: 10.1242/jcs.009977
pubmed: 17698920
Krishnan B, Thomas SE, Yan R, Yamada H, Zhulin IB, McKee BD. Sisters unbound is required for meiotic centromeric cohesion in Drosophila melanogaster. Genetics. 2014;198(3):947–65. https://doi.org/10.1534/genetics.114.166009 .
doi: 10.1534/genetics.114.166009
pubmed: 25194162
pmcid: 4224182
Yan R, McKee BD. The cohesion protein SOLO associates with SMC1 and is required for synapsis, recombination, homolog bias and cohesion and pairing of centromeres in Drosophila meiosis. PLoS Genet. 2013;9(7):e1003637. https://doi.org/10.1371/journal.pgen.1003637 .
doi: 10.1371/journal.pgen.1003637
pubmed: 23874232
pmcid: 3715423
Chiang T, Duncan FE, Schindler K, Schultz RM, Lampson MA. Evidence that weakened centromere cohesion is a leading cause of age-related aneuploidy in oocytes. Curr Biol. 2010;20(17):1522–8. https://doi.org/10.1016/j.cub.2010.06.069 .
doi: 10.1016/j.cub.2010.06.069
pubmed: 20817534
pmcid: 2939204
Lister LM, Kouznetsova A, Hyslop LA, Kalleas D, Pace SL, Barel JC, et al. Age-related meiotic segregation errors in mammalian oocytes are preceded by depletion of cohesin and Sgo2. Curr Biol. 2010;20(17):1511–21. https://doi.org/10.1016/j.cub.2010.08.023 .
doi: 10.1016/j.cub.2010.08.023
pubmed: 20817533
Stemmann O, Zou H, Gerber SA, Gygi SP, Kirschner MW. Dual inhibition of sister chromatid separation at metaphase. Cell. 2001;107(6):715–26. https://doi.org/10.1016/s0092-8674(01)00603-1 .
doi: 10.1016/s0092-8674(01)00603-1
pubmed: 11747808
Chiang T, Schultz RM, Lampson MA. Age-dependent susceptibility of chromosome cohesion to premature separase activation in mouse oocytes. Biol Reprod. 2011;85(6):1279–83. https://doi.org/10.1095/biolreprod.111.094094 .
doi: 10.1095/biolreprod.111.094094
pubmed: 21865557
pmcid: 3223255
Nabti I, Grimes R, Sarna H, Marangos P, Carroll J. Maternal age-dependent APC/C-mediated decrease in securin causes premature sister chromatid separation in meiosis II. Nat Commun. 2017;8:15346. https://doi.org/10.1038/ncomms15346 .
doi: 10.1038/ncomms15346
pubmed: 28516917
pmcid: 5454377
Burkhardt S, Borsos M, Szydlowska A, Godwin J, Williams SA, Cohen PE, et al. Chromosome cohesion established by Rec8-cohesin in fetal oocytes is maintained without detectable turnover in oocytes arrested for months in mice. Curr Biol. 2016;26(5):678–85. https://doi.org/10.1016/j.cub.2015.12.073 .
doi: 10.1016/j.cub.2015.12.073
pubmed: 26898469
pmcid: 4791431
Severson AF, Meyer BJ. Divergent kleisin subunits of cohesin specify mechanisms to tether and release meiotic chromosomes. Elife. 2014;3:e03467. https://doi.org/10.7554/eLife.03467 .
doi: 10.7554/eLife.03467
pubmed: 25171895
pmcid: 4174578
Unal E, Heidinger-Pauli JM, Koshland D. DNA double-strand breaks trigger genome-wide sister-chromatid cohesion through Eco1 (Ctf7). Science. 2007;317(5835):245–8. https://doi.org/10.1126/science.1140637 .
doi: 10.1126/science.1140637
pubmed: 17626885
Perkins AT, Bickel SE. Using fluorescence in situ hybridization (FISH) to monitor the state of arm cohesion in prometaphase and metaphase I Drosophila oocytes. J Vis Exp. 2017;130. https://doi.org/10.3791/56802 .
Perkins AT, Greig MM, Sontakke AA, Peloquin AS, McPeek MA, Bickel SE. Increased levels of superoxide dismutase suppress meiotic segregation errors in aging oocytes. Chromosoma. 2019;128(3):215–22. https://doi.org/10.1007/s00412-019-00702-y .
doi: 10.1007/s00412-019-00702-y
pubmed: 31037468
pmcid: 6823651
Yun Y, Wei Z, Hunter N. Maternal obesity enhances oocyte chromosome abnormalities associated with aging. Chromosoma. 2019;128(3):413–21. https://doi.org/10.1007/s00412-019-00716-6 .
doi: 10.1007/s00412-019-00716-6
pubmed: 31286204
Cheng S, Lu Y, Liu G, Wang SQ. Finite cohesion due to chain entanglement in polymer melts. Soft Matter. 2016;12(14):3340–51. https://doi.org/10.1039/c6sm00142d .
doi: 10.1039/c6sm00142d
pubmed: 26931322
Watanabe Y, Nurse P. Cohesin Rec8 is required for reductional chromosome segregation at meiosis. Nature. 1999;400(6743):461–4. https://doi.org/10.1038/22774 .
doi: 10.1038/22774
pubmed: 10440376
Zielinska AP, Bellou E, Sharma N, Frombach AS, Seres KB, Gruhn JR, et al. Meiotic kinetochores fragment into multiple lobes upon cohesin loss in aging eggs. Curr Biol. 2019;29(22):3749–65 e7. https://doi.org/10.1016/j.cub.2019.09.006 .
doi: 10.1016/j.cub.2019.09.006
pubmed: 31679939
pmcid: 6868511
Kitajima TS, Ohsugi M, Ellenberg J. Complete kinetochore tracking reveals error-prone homologous chromosome biorientation in mammalian oocytes. Cell. 2011;146(4):568–81. https://doi.org/10.1016/j.cell.2011.07.031 .
doi: 10.1016/j.cell.2011.07.031
pubmed: 21854982
Watanabe Y. Geometry and force behind kinetochore orientation: lessons from meiosis. Nat Rev Mol Cell Biol. 2012;13(6):370–82. https://doi.org/10.1038/nrm3349 .
doi: 10.1038/nrm3349
pubmed: 22588367
Cimini D, Howell B, Maddox P, Khodjakov A, Degrassi F, Salmon ED. Merotelic kinetochore orientation is a major mechanism of aneuploidy in mitotic mammalian tissue cells. J Cell Biol. 2001;153(3):517–27. https://doi.org/10.1083/jcb.153.3.517 .
doi: 10.1083/jcb.153.3.517
pubmed: 11331303
pmcid: 2190575
Shomper M, Lappa C, FitzHarris G. Kinetochore microtubule establishment is defective in oocytes from aged mice. Cell Cycle. 2014;13(7):1171–9. https://doi.org/10.4161/cc.28046 .
doi: 10.4161/cc.28046
pubmed: 24553117
pmcid: 4013167
Cheng JM, Liu YX. Age-related loss of cohesion: causes and effects. Int J Mol Sci. 2017;18(7). https://doi.org/10.3390/ijms18071578 .
Baker DJ, Jeganathan KB, Cameron JD, Thompson M, Juneja S, Kopecka A, et al. BubR1 insufficiency causes early onset of aging-associated phenotypes and infertility in mice. Nat Genet. 2004;36(7):744–9. https://doi.org/10.1038/ng1382 .
doi: 10.1038/ng1382
pubmed: 15208629
Shimoi G, Tomita M, Kataoka M, Kameyama Y. Destabilization of spindle assembly checkpoint causes aneuploidy during meiosis II in murine post-ovulatory aged oocytes. J Reprod Dev. 2019;65(1):57–66. https://doi.org/10.1262/jrd.2018-056 .
doi: 10.1262/jrd.2018-056
pubmed: 30464155
Steuerwald N, Cohen J, Herrera RJ, Sandalinas M, Brenner CA. Association between spindle assembly checkpoint expression and maternal age in human oocytes. Mol Hum Reprod. 2001;7(1):49–55. https://doi.org/10.1093/molehr/7.1.49 .
doi: 10.1093/molehr/7.1.49
pubmed: 11134360
Collins JK, Lane SIR, Merriman JA, Jones KT. DNA damage induces a meiotic arrest in mouse oocytes mediated by the spindle assembly checkpoint. Nat Commun. 2015;6:8553. https://doi.org/10.1038/ncomms9553 .
doi: 10.1038/ncomms9553
pubmed: 26522232
pmcid: 4659839
Lane SIR, Morgan SL, Wu T, Collins JK, Merriman JA, ElInati E, et al. DNA damage induces a kinetochore-based ATM/ATR-independent SAC arrest unique to the first meiotic division in mouse oocytes. Development. 2017;144(19):3475–86. https://doi.org/10.1242/dev.153965 .
doi: 10.1242/dev.153965
pubmed: 28851706
pmcid: 5665484
Marangos P, Stevense M, Niaka K, Lagoudaki M, Nabti I, Jessberger R, et al. DNA damage-induced metaphase I arrest is mediated by the spindle assembly checkpoint and maternal age. Nat Commun. 2015;6:8706. https://doi.org/10.1038/ncomms9706 .
doi: 10.1038/ncomms9706
pubmed: 26522734
pmcid: 4667640
Grell EH. Genetic analysis of aspartate aminotransferase isozymes from hybrids between Drosophila melanogaster and Drosophila simulans and mutagen-induced isozyme variants. Genetics. 1976;83(4):753–64.
pubmed: 823072
pmcid: 1213549
Hawley RS, Irick H, Zitron AE, Haddox DA, Lohe A, New C, et al. There are two mechanisms of achiasmate segregation in Drosophila females, one of which requires heterochromatic homology. Dev Genet. 1992;13(6):440–67. https://doi.org/10.1002/dvg.1020130608 .
doi: 10.1002/dvg.1020130608
pubmed: 1304424
Karpen GH, Le MH, Le H. Centric heterochromatin and the efficiency of achiasmate disjunction in Drosophila female meiosis. Science. 1996;273(5271):118–22. https://doi.org/10.1126/science.273.5271.118 .
doi: 10.1126/science.273.5271.118
pubmed: 8658180
Dernburg AF, Sedat JW, Hawley RS. Direct evidence of a role for heterochromatin in meiotic chromosome segregation. Cell. 1996;86(1):135–46. https://doi.org/10.1016/s0092-8674(00)80084-7 .
doi: 10.1016/s0092-8674(00)80084-7
pubmed: 8689681
Hughes SE, Gilliland WD, Cotitta JL, Takeo S, Collins KA, Hawley RS. Heterochromatic threads connect oscillating chromosomes during prometaphase I in Drosophila oocytes. PLoS Genet. 2009;5(1):e1000348. https://doi.org/10.1371/journal.pgen.1000348 .
doi: 10.1371/journal.pgen.1000348
pubmed: 19165317
pmcid: 2615114
Giauque CC, Bickel SE. Heterochromatin-associated proteins HP1a and Piwi collaborate to maintain the association of achiasmate homologs in Drosophila oocytes. Genetics. 2016;203(1):173–89. https://doi.org/10.1534/genetics.115.186460 .
doi: 10.1534/genetics.115.186460
pubmed: 26984058
pmcid: 4858772
Hughes SE, Miller DE, Miller AL, Hawley RS. Female meiosis: synapsis, recombination, and segregation in Drosophila melanogaster. Genetics. 2018;208(3):875–908. https://doi.org/10.1534/genetics.117.300081 .
doi: 10.1534/genetics.117.300081
pubmed: 29487146
pmcid: 5844340
Fledel-Alon A, Wilson DJ, Broman K, Wen X, Ober C, Coop G, et al. Broad-scale recombination patterns underlying proper disjunction in humans. PLoS Genet. 2009;5(9):e1000658. https://doi.org/10.1371/journal.pgen.1000658 .
doi: 10.1371/journal.pgen.1000658
pubmed: 19763175
pmcid: 2734982
Koehler KE, Hassold TJ. Human aneuploidy: lessons from achiasmate segregation in Drosophila melanogaster. Ann Hum Genet. 1998;62(Pt 6):467–79. https://doi.org/10.1046/j.1469-1809.1998.6260467.x .
doi: 10.1046/j.1469-1809.1998.6260467.x
pubmed: 10363125
Bisig CG, Guiraldelli MF, Kouznetsova A, Scherthan H, Hoog C, Dawson DS, et al. Synaptonemal complex components persist at centromeres and are required for homologous centromere pairing in mouse spermatocytes. PLoS Genet. 2012;8(6):e1002701. https://doi.org/10.1371/journal.pgen.1002701 .
doi: 10.1371/journal.pgen.1002701
pubmed: 22761579
pmcid: 3386160
Qiao H, Chen JK, Reynolds A, Hoog C, Paddy M, Hunter N. Interplay between synaptonemal complex, homologous recombination, and centromeres during mammalian meiosis. PLoS Genet. 2012;8(6):e1002790. https://doi.org/10.1371/journal.pgen.1002790 .
doi: 10.1371/journal.pgen.1002790
pubmed: 22761591
pmcid: 3386176
Previato de Almeida L, Evatt JM, Chuong HH, Kurdzo EL, Eyster CA, Gladstone MN, et al. Shugoshin protects centromere pairing and promotes segregation of nonexchange partner chromosomes in meiosis. Proc Natl Acad Sci U S A. 2019;116(19):9417–22. https://doi.org/10.1073/pnas.1902526116 .
doi: 10.1073/pnas.1902526116
pubmed: 31019073
pmcid: 6511000
Capalbo A, Hoffmann ER, Cimadomo D, Ubaldi FM, Rienzi L. Human female meiosis revised: new insights into the mechanisms of chromosome segregation and aneuploidies from advanced genomics and time-lapse imaging. Hum Reprod Update. 2017;23(6):706–22. https://doi.org/10.1093/humupd/dmx026 .
doi: 10.1093/humupd/dmx026
pubmed: 28961822
Ottolini CS, Capalbo A, Newnham L, Cimadomo D, Natesan SA, Hoffmann ER, et al. Generation of meiomaps of genome-wide recombination and chromosome segregation in human oocytes. Nat Protoc. 2016;11(7):1229–43. https://doi.org/10.1038/nprot.2016.075 .
doi: 10.1038/nprot.2016.075
pubmed: 27310263
Vargas E, McNally K, Friedman JA, Cortes DB, Wang DY, Korf IF, et al. Autosomal trisomy and triploidy are corrected during female meiosis in Caenorhabditis elegans. Genetics. 2017;207(3):911–22. https://doi.org/10.1534/genetics.117.300259 .
doi: 10.1534/genetics.117.300259
pubmed: 28882988
pmcid: 5676225
López-Otín C, Blasco MA, Partridge L, Serrano M, Kroemer G. The hallmarks of aging. Cell. 2013;153(6):1194–217. https://doi.org/10.1016/j.cell.2013.05.039 .
doi: 10.1016/j.cell.2013.05.039
pubmed: 23746838
pmcid: 3836174
Kushnir VA, Ludaway T, Russ RB, Fields EJ, Koczor C, Lewis W. Reproductive aging is associated with decreased mitochondrial abundance and altered structure in murine oocytes. J Assist Reprod Genet. 2012;29(7):637–42. https://doi.org/10.1007/s10815-012-9771-5 .
doi: 10.1007/s10815-012-9771-5
pubmed: 22527902
pmcid: 3401248
Simsek-Duran F, Li F, Ford W, Swanson RJ, Jones HW, Castora FJ. Age-associated metabolic and morphologic changes in mitochondria of individual mouse and hamster oocytes. PLoS One. 2013;8(5):e64955. https://doi.org/10.1371/journal.pone.0064955 .
doi: 10.1371/journal.pone.0064955
pubmed: 23741435
pmcid: 3669215
Erwin AA, Blumenstiel JP. Aging in the Drosophila ovary: contrasting changes in the expression of the piRNA machinery and mitochondria but no global release of transposable elements. BMC Genomics. 2019;20(1):305. https://doi.org/10.1186/s12864-019-5668-3 .
doi: 10.1186/s12864-019-5668-3
pubmed: 31014230
pmcid: 6480902
Bohnert KA, Kenyon C. A lysosomal switch triggers proteostasis renewal in the immortal C. elegans germ lineage. Nature. 2017;551(7682):629–63.
doi: 10.1038/nature24620
Murakoshi Y, Sueoka K, Takahashi K, Sato S, Sakurai T, Tajima H, et al. Embryo developmental capability and pregnancy outcome are related to the mitochondrial DNA copy number and ooplasmic volume. J Assist Reprod Genet. 2013;30(10):1367–75. https://doi.org/10.1007/s10815-013-0062-6 .
doi: 10.1007/s10815-013-0062-6
pubmed: 23897005
pmcid: 3824848
Peluso JJ, Butcher RL. The effect of follicular aging on the ultrastructure of the rat oocyte. Fertil Steril. 1974;25(6):494–502.
doi: 10.1016/S0015-0282(16)40453-X
Müller-Höcker J, Schäfer S, Weis S, Münscher C, Strowitzki T. Morphological-cytochemical and molecular genetic analyses of mitochondria in isolated human oocytes in the reproductive age. Mol Hum Reprod. 1996;2(12):951–8. https://doi.org/10.1093/molehr/2.12.951 .
doi: 10.1093/molehr/2.12.951
pubmed: 9237239
Tarín JJ, Pérez-Albalá S, Cano A. Cellular and morphological traits of oocytes retrieved from aging mice after exogenous ovarian stimulation. Biol Reprod. 2001;65(1):141–50. https://doi.org/10.1095/biolreprod65.1.141 .
doi: 10.1095/biolreprod65.1.141
pubmed: 11420234
Tilly JL, Sinclair DA. Germline energetics, aging, and female infertility. Cell Metab. 2013;17(6):838–50. https://doi.org/10.1016/j.cmet.2013.05.007 .
doi: 10.1016/j.cmet.2013.05.007
pubmed: 23747243
pmcid: 3756096
Hamatani T, Falco G, Carter MG, Akutsu H, Stagg CA, Sharov AA, et al. Age-associated alteration of gene expression patterns in mouse oocytes. Hum Mol Genet. 2004;13(19):2263–78. https://doi.org/10.1093/hmg/ddh241 .
doi: 10.1093/hmg/ddh241
pubmed: 15317747
Ben-Meir A, Burstein E, Borrego-Alvarez A, Chong J, Wong E, Yavorska T, et al. Coenzyme Q10 restores oocyte mitochondrial function and fertility during reproductive aging. Aging Cell. 2015;14(5):887–95. https://doi.org/10.1111/acel.12368 .
doi: 10.1111/acel.12368
pubmed: 26111777
pmcid: 4568976
Tatone C, Carbone MC, Falone S, Aimola P, Giardinelli A, Caserta D, et al. Age-dependent changes in the expression of superoxide dismutases and catalase are associated with ultrastructural modifications in human granulosa cells. Mol Hum Reprod. 2006;12(11):655–60. https://doi.org/10.1093/molehr/gal080 .
doi: 10.1093/molehr/gal080
pubmed: 17005595
Wang S, Zheng Y, Li J, Yu Y, Zhang W, Song M, et al. Single-cell transcriptomic atlas of primate ovarian aging. Cell. 2020;180(3):585-600.e19. https://doi.org/10.1016/j.cell.2020.01.009 .
doi: 10.1016/j.cell.2020.01.009
pubmed: 32004457
Tsakiri EN, Sykiotis GP, Papassideri IS, Gorgoulis VG, Bohmann D, Trougakos IP. Differential regulation of proteasome functionality in reproductive vs. somatic tissues of Drosophila during aging or oxidative stress. FASEB J. 2013;27(6):2407–20. https://doi.org/10.1096/fj.12-221408 .
doi: 10.1096/fj.12-221408
pubmed: 23457214
pmcid: 4050428
Lim J, Luderer U. Oxidative damage increases and antioxidant gene expression decreases with aging in the mouse ovary. Biol Reprod. 2011;84(4):775–82. https://doi.org/10.1095/biolreprod.110.088583 .
doi: 10.1095/biolreprod.110.088583
pubmed: 21148108
Matos L, Stevenson D, Gomes F, Silva-Carvalho JL, Almeida H. Superoxide dismutase expression in human cumulus oophorus cells. Mol Hum Reprod. 2009;15(7):411–9. https://doi.org/10.1093/molehr/gap034 .
doi: 10.1093/molehr/gap034
pubmed: 19482907
Peters AE, Mihalas BP, Bromfield EG, Roman SD, Nixon B, Sutherland JM. Autophagy in female fertility: a role in oxidative stress and aging. Antioxid Redox Signal. 2020;32(8):550–68. https://doi.org/10.1089/ars.2019.7986 .
doi: 10.1089/ars.2019.7986
pubmed: 31892284
Cai H, Li Y, Li H, Niringiyumukiza JD, Zhang M, Chen L, et al. Identification and characterization of human ovary-derived circular RNAs and their potential roles in ovarian aging. Aging (Albany NY). 2018;10(9):2511–34. https://doi.org/10.18632/aging.101565 .
doi: 10.18632/aging.101565
Zhang X, Wu XQ, Lu S, Guo YL, Ma X. Deficit of mitochondria-derived ATP during oxidative stress impairs mouse MII oocyte spindles. Cell Res. 2006;16(10):841–50. https://doi.org/10.1038/sj.cr.7310095 .
doi: 10.1038/sj.cr.7310095
pubmed: 16983401
Wilding M, Dale B, Marino M, di Matteo L, Alviggi C, Pisaturo ML, et al. Mitochondrial aggregation patterns and activity in human oocytes and preimplantation embryos. Hum Reprod. 2001;16(5):909–17. https://doi.org/10.1093/humrep/16.5.909 .
doi: 10.1093/humrep/16.5.909
pubmed: 11331637
Fragouli E, Spath K, Alfarawati S, Kaper F, Craig A, Michel CE, et al. Altered levels of mitochondrial DNA are associated with female age, aneuploidy, and provide an independent measure of embryonic implantation potential. PLoS Genet. 2015;11(6):e1005241. https://doi.org/10.1371/journal.pgen.1005241 .
doi: 10.1371/journal.pgen.1005241
pubmed: 26039092
pmcid: 4454688
Faraci C, Annis S, Jin J, Li H, Khrapko K, Woods DC. Impact of exercise on oocyte quality in the POLG mitochondrial DNA mutator mouse. Reproduction. 2018;156(2):185–94. https://doi.org/10.1530/REP-18-0061 .
doi: 10.1530/REP-18-0061
pubmed: 29875308
pmcid: 6074767
Tarín JJ, Pérez-Albalá S, Cano A. Oral antioxidants counteract the negative effects of female aging on oocyte quantity and quality in the mouse. Molecular Reproduction and Development. 2002;61(3).
Bertoldo MJ, Listijono DR, Ho WJ, Riepsamen AH, Goss DM, Richani D, et al. NAD+ repletion rescues female fertility during reproductive aging. Cell Rep. 2020;30(6):1670-81.e7. https://doi.org/10.1016/j.celrep.2020.01.058 .
doi: 10.1016/j.celrep.2020.01.058
Amaral S, Mota P, Rodrigues AS, Martins L, Oliveira PJ, Ramalho-Santos J. Testicular aging involves mitochondrial dysfunction as well as an increase in UCP2 levels and proton leak. FEBS Lett. 2008;582(30):4191–6. https://doi.org/10.1016/j.febslet.2008.11.020 .
doi: 10.1016/j.febslet.2008.11.020
pubmed: 19041646
Weir CP, Robaire B. Spermatozoa have decreased antioxidant enzymatic capacity and increased reactive oxygen species production during aging in the Brown Norway rat. J Androl. 2007;28(2):229–40. https://doi.org/10.2164/jandrol.106.001362 .
doi: 10.2164/jandrol.106.001362
pubmed: 17021340
Liao CH, Chen BH, Chiang HS, Chen CW, Chen MF, Ke CC, et al. Optimizing a male reproductive aging mouse model by D-galactose injection. Int J Mol Sci. 2016;17(1). https://doi.org/10.3390/ijms17010098 .
Liu J, Liu M, Ye X, Liu K, Huang J, Wang L, et al. Delay in oocyte aging in mice by the antioxidant N-acetyl-L-cysteine (NAC). Hum Reprod. 2012;27(5):1411–20. https://doi.org/10.1093/humrep/des019 .
doi: 10.1093/humrep/des019
pubmed: 22357770
Zhang M, Lu Y, Chen Y, Zhang Y, Xiong B. Insufficiency of melatonin in follicular fluid is a reversible cause for advanced maternal age-related aneuploidy in oocytes. Redox Biol. 2020;28:101327. https://doi.org/10.1016/j.redox.2019.101327 .
doi: 10.1016/j.redox.2019.101327
pubmed: 31526949
Meyer JN, Boyd WA, Azzam GA, Haugen AC, Freedman JH, Van Houten B. Decline of nucleotide excision repair capacity in aging Caenorhabditis elegans. Genome Biol. 2007;8(5):R70. https://doi.org/10.1186/gb-2007-8-5-r70 .
doi: 10.1186/gb-2007-8-5-r70
pubmed: 17472752
pmcid: 1929140
Hasty P, Campisi J, Hoeijmakers J, van Steeg H, Vijg J. Aging and genome maintenance: lessons from the mouse? Science. 2003;299(5611):1355–9. https://doi.org/10.1126/science.1079161 .
doi: 10.1126/science.1079161
pubmed: 12610296
Lombard DB, Chua KF, Mostoslavsky R, Franco S, Gostissa M, Alt FW. DNA repair, genome stability, and aging. Cell. 2005;120(4):497–512. https://doi.org/10.1016/j.cell.2005.01.028 .
doi: 10.1016/j.cell.2005.01.028
pubmed: 15734682
Goukassian D, Gad F, Yaar M, Eller MS, Nehal US, Gilchrest BA. Mechanisms and implications of the age-associated decrease in DNA repair capacity. FASEB J. 2000;14(10):1325–34. https://doi.org/10.1096/fj.14.10.1325 .
doi: 10.1096/fj.14.10.1325
pubmed: 10877825
Wylie A, Lu WJ, D'Brot A, Buszczak M, Abrams JM. p53 activity is selectively licensed in the Drosophila stem cell compartment. Elife. 2014;3:e01530. https://doi.org/10.7554/eLife.01530 .
doi: 10.7554/eLife.01530
pubmed: 24618896
pmcid: 3949305
Xing Y, Su TT, Ruohola-Baker H. Tie-mediated signal from apoptotic cells protects stem cells in Drosophila melanogaster. Nat Commun. 2015;6:7058. https://doi.org/10.1038/ncomms8058 .
doi: 10.1038/ncomms8058
pubmed: 25959206
pmcid: 4451836
Artoni F, Kreipke RE, Palmeira O, Dixon C, Goldberg Z, Ruohola-Baker H. Loss of foxo rescues stem cell aging in Drosophila germ line. Elife. 2017;6. https://doi.org/10.7554/eLife.27842 .
Titus S, Li F, Stobezki R, Akula K, Unsal E, Jeong K, et al. Impairment of BRCA1-related DNA double-strand break repair leads to ovarian aging in mice and humans. Sci Transl Med. 2013;5(172):172ra21. https://doi.org/10.1126/scitranslmed.3004925 .
doi: 10.1126/scitranslmed.3004925
pubmed: 23408054
pmcid: 5130338
Titus S, Stobezki R, Oktay K. Impaired DNA repair as a mechanism for oocyte aging: is it epigenetically determined? Semin Reprod Med. 2015;33(6):384–8. https://doi.org/10.1055/s-0035-1567824 .
doi: 10.1055/s-0035-1567824
pubmed: 26562289
Govindaraj V, Keralapura Basavaraju R, Rao AJ. Changes in the expression of DNA double strand break repair genes in primordial follicles from immature and aged rats. Reprod Biomed Online. 2015;30(3):303–10. https://doi.org/10.1016/j.rbmo.2014.11.010 .
doi: 10.1016/j.rbmo.2014.11.010
pubmed: 25599822
Zhang D, Zhang X, Zeng M, Yuan J, Liu M, Yin Y, et al. Increased DNA damage and repair deficiency in granulosa cells are associated with ovarian aging in rhesus monkey. J Assist Reprod Genet. 2015;32(7):1069–78. https://doi.org/10.1007/s10815-015-0483-5 .
doi: 10.1007/s10815-015-0483-5
pubmed: 25957622
pmcid: 4531862
Bhargava V, Goldstein CD, Russell L, Xu L, Ahmed M, Li W, et al. GCNA preserves genome integrity and fertility across species. Dev Cell. 2020;52(1):38–52 e10. https://doi.org/10.1016/j.devcel.2019.11.007 .
doi: 10.1016/j.devcel.2019.11.007
pubmed: 31839537
Degtyareva NP, Greenwell P, Hofmann ER, Hengartner MO, Zhang L, Culotti JG, et al. Caenorhabditis elegans DNA mismatch repair gene msh-2 is required for microsatellite stability and maintenance of genome integrity. Proc Natl Acad Sci U S A. 2002;99(4):2158–63. https://doi.org/10.1073/pnas.032671599 .
doi: 10.1073/pnas.032671599
pubmed: 11830642
pmcid: 122335
Kalmbach KH, Antunes DM, Kohlrausch F, Keefe DL. Telomeres and female reproductive aging. Semin Reprod Med. 2015;33(6):389–95. https://doi.org/10.1055/s-0035-1567823 .
doi: 10.1055/s-0035-1567823
pubmed: 26629734
de Lange T. Shelterin: the protein complex that shapes and safeguards human telomeres. Genes Dev. 2005;19(18):2100–10. https://doi.org/10.1101/gad.1346005 .
doi: 10.1101/gad.1346005
pubmed: 16166375
Liu L, Trimarchi JR, Smith PJ, Keefe DL. Mitochondrial dysfunction leads to telomere attrition and genomic instability. Aging Cell. 2002;1(1):40–6. https://doi.org/10.1046/j.1474-9728.2002.00004.x .
doi: 10.1046/j.1474-9728.2002.00004.x
pubmed: 12882352
Keefe DL, Liu L. Telomeres and reproductive aging. Reprod Fertil Dev. 2009;21(1):10–4. https://doi.org/10.1071/rd08229 .
doi: 10.1071/rd08229
pubmed: 19152740
Keefe DL, Liu L, Marquard K. Telomeres and aging-related meiotic dysfunction in women. Cell Mol Life Sci. 2007;64(2):139–43. https://doi.org/10.1007/s00018-006-6466-z .
doi: 10.1007/s00018-006-6466-z
pubmed: 17219022
Rocca MS, Foresta C, Ferlin A. Telomere length: lights and shadows on their role in human reproduction. Biol Reprod. 2019;100(2):305–17. https://doi.org/10.1093/biolre/ioy208 .
doi: 10.1093/biolre/ioy208
pubmed: 30277496
Yamada-Fukunaga T, Yamada M, Hamatani T, Chikazawa N, Ogawa S, Akutsu H, et al. Age-associated telomere shortening in mouse oocytes. Reprod Biol Endocrinol. 2013;11:108. https://doi.org/10.1186/1477-7827-11-108 .
doi: 10.1186/1477-7827-11-108
pubmed: 24261933
pmcid: 3842639
Zhang JM, Zou L. Alternative lengthening of telomeres: from molecular mechanisms to therapeutic outlooks. Cell Biosci. 2020;10:30. https://doi.org/10.1186/s13578-020-00391-6 .
doi: 10.1186/s13578-020-00391-6
pubmed: 32175073
pmcid: 7063710
Yanowitz JL. Genome integrity is regulated by the Caenorhabditis elegans Rad51D homolog rfs-1. Genetics. 2008;179(1):249–62. https://doi.org/10.1534/genetics.107.076877 .
doi: 10.1534/genetics.107.076877
pubmed: 18458109
pmcid: 2390604
Sinnige T, Yu A, Morimoto RI. Challenging proteostasis: role of the chaperone network to control aggregation-prone proteins in human disease. Adv Exp Med Biol. 2020;1243:53–68. https://doi.org/10.1007/978-3-030-40204-4_4 .
doi: 10.1007/978-3-030-40204-4_4
pubmed: 32297211
Noormohammadi A, Calculli G, Gutierrez-Garcia R, Khodakarami A, Koyuncu S, Vilchez D. Mechanisms of protein homeostasis (proteostasis) maintain stem cell identity in mammalian pluripotent stem cells. Cell Mol Life Sci. 2018;75(2):275–90. https://doi.org/10.1007/s00018-017-2602-1 .
doi: 10.1007/s00018-017-2602-1
pubmed: 28748323
Fredriksson Å, Johansson Krogh E, Hernebring M, Pettersson E, Javadi A, Almstedt A, et al. Effects of aging and reproduction on protein quality control in soma and gametes of Drosophila melanogaster. Aging Cell. 2012;11(4):634–43. https://doi.org/10.1111/j.1474-9726.2012.00823.x .
doi: 10.1111/j.1474-9726.2012.00823.x
pubmed: 22507075
Goudeau J, Aguilaniu H. Carbonylated proteins are eliminated during reproduction in C. elegans. Aging Cell. 2010;9(6):991–1003. https://doi.org/10.1111/j.1474-9726.2010.00625.x .
doi: 10.1111/j.1474-9726.2010.00625.x
pubmed: 21040398
Hernebring M, Brole’ G, Aguilaniu H, Semb H, Nystro T. Elimination of damaged proteins during differentiation of embryonic stem cells. PNAS. 2015:7700–5.
Yao Q, Liang Y, Shao Y, Bian W, Fu H, Xu J, et al. Advanced glycation end product concentrations in follicular fluid of women undergoing IVF/ICSI with a GnRH agonist protocol. Reprod Biomed Online. 2018;36(1):20–5. https://doi.org/10.1016/j.rbmo.2017.09.003 .
doi: 10.1016/j.rbmo.2017.09.003
pubmed: 29174168
Sato M, Sato K. Degradation of paternal mitochondria by fertilization-triggered autophagy in C. elegans embryos. Science. 2011;334(6059):1141–4. https://doi.org/10.1126/science.1210333 .
doi: 10.1126/science.1210333
pubmed: 21998252
Sharpley MS, Marciniak C, Eckel-Mahan K, McManus M, Crimi M, Waymire K, et al. Heteroplasmy of mouse mtDNA is genetically unstable and results in altered behavior and cognition. Cell. 2012;151(2):333–43. https://doi.org/10.1016/j.cell.2012.09.004 .
doi: 10.1016/j.cell.2012.09.004
pubmed: 23063123
pmcid: 4175720
Politi Y, Gal L, Kalifa Y, Ravid L, Elazar Z, Arama E. Paternal mitochondrial destruction after fertilization is mediated by a common endocytic and autophagic pathway in Drosophila. Dev Cell. 2014;29(3):305–20. https://doi.org/10.1016/j.devcel.2014.04.005 .
doi: 10.1016/j.devcel.2014.04.005
pubmed: 24823375
Kimura M, Itoh N, Takagi S, Sasao T, Takahashi A, Masumori N, et al. Balance of apoptosis and proliferation of germ cells related to spermatogenesis in aged men. J Androl. 2003;24(2):185–91. https://doi.org/10.1002/j.1939-4640.2003.tb02661.x .
doi: 10.1002/j.1939-4640.2003.tb02661.x
pubmed: 12634304
David DC, Ollikainen N, Trinidad JC, Cary MP, Burlingame AL, Kenyon C. Widespread protein aggregation as an inherent part of aging in C. elegans. PLoS Biol. 2010;8(8):e1000450. https://doi.org/10.1371/journal.pbio.1000450 .
doi: 10.1371/journal.pbio.1000450
pubmed: 20711477
pmcid: 2919420
Mihalas BP, Bromfield EG, Sutherland JM, De Iuliis GN, McLaughlin EA, Aitken RJ, et al. Oxidative damage in naturally aged mouse oocytes is exacerbated by dysregulation of proteasomal activity. J Biol Chem. 2018;293(49):18944–64. https://doi.org/10.1074/jbc.RA118.005751 .
doi: 10.1074/jbc.RA118.005751
pubmed: 30305393
pmcid: 6295717
Zimmerman SM, Hinkson IV, Elias JE, Kim SK. Reproductive aging drives protein accumulation in the uterus and limits lifespan in C. elegans. PLoS Genet. 2015;11(12):e1005725. https://doi.org/10.1371/journal.pgen.1005725 .
doi: 10.1371/journal.pgen.1005725
pubmed: 26656270
pmcid: 4676719
Andaloussi AE, Habib S, Soylemes G, Laknaur A, Elhusseini H, Al-Hendy A, et al. Defective expression of ATG4D abrogates autophagy and promotes growth in human uterine fibroids. Cell Death Discov. 2017;3:17041. https://doi.org/10.1038/cddiscovery.2017.41 .
doi: 10.1038/cddiscovery.2017.41
pubmed: 28815060
pmcid: 5554887
Duncan FE, Jasti S, Paulson A, Kelsh JM, Fegley B, Gerton JL. Age-associated dysregulation of protein metabolism in the mammalian oocyte. Aging Cell. 2017;16(6):1381–93. https://doi.org/10.1111/acel.12676 .
doi: 10.1111/acel.12676
pubmed: 28994181
pmcid: 5676066
Assou S, Cerecedo D, Tondeur S, Pantesco V, Hovatta O, Klein B, et al. A gene expression signature shared by human mature oocytes and embryonic stem cells. BMC Genomics. 2009;10:10. https://doi.org/10.1186/1471-2164-10-10 .
doi: 10.1186/1471-2164-10-10
pubmed: 19128516
pmcid: 2628676
Tamura H, Kawamoto M, Sato S, Tamura I, Maekawa R, Taketani T, et al. Long-term melatonin treatment delays ovarian aging. J Pineal Res. 2017;62(2). https://doi.org/10.1111/jpi.12381 .
Meneau F, Dupre A, Jessus C, Daldello EM. Translational control of Xenopus oocyte meiosis: toward the genomic era. Cells. 2020;9(6). https://doi.org/10.3390/cells9061502 .
Greenblatt EJ, Obniski R, Mical C, Spradling AC. Prolonged ovarian storage of mature Drosophila oocytes dramatically increases meiotic spindle instability. Elife. 2019;8. https://doi.org/10.7554/eLife.49455 .
Greenblatt EJ, Spradling AC. Fragile X mental retardation 1 gene enhances the translation of large autism-related proteins. Science. 2018;361(6403):709–12. https://doi.org/10.1126/science.aas9963 .
doi: 10.1126/science.aas9963
pubmed: 30115809
pmcid: 6905618
Crosnoe LE, Kim ED. Impact of age on male fertility. Curr Opin Obstet Gynecol. 2013;25(3):181–5. https://doi.org/10.1097/GCO.0b013e32836024cb .
doi: 10.1097/GCO.0b013e32836024cb
pubmed: 23493186
Fonseka KG, Griffin DK. Is there a paternal age effect for aneuploidy? Cytogenet Genome Res. 2011;133(2-4):280–91. https://doi.org/10.1159/000322816 .
doi: 10.1159/000322816
pubmed: 21212646
Gao Z, Moorjani P, Sasani TA, Pedersen BS, Quinlan AR, Jorde LB, et al. Overlooked roles of DNA damage and maternal age in generating human germline mutations. Proc Natl Acad Sci U S A. 2019;116(19):9491–500. https://doi.org/10.1073/pnas.1901259116 .
doi: 10.1073/pnas.1901259116
pubmed: 31019089
pmcid: 6511033
Jenkins TG, Aston KI, Pflueger C, Cairns BR, Carrell DT. Age-associated sperm DNA methylation alterations: possible implications in offspring disease susceptibility. PLoS Genet. 2014;10(7):e1004458. https://doi.org/10.1371/journal.pgen.1004458 .
doi: 10.1371/journal.pgen.1004458
pubmed: 25010591
pmcid: 4091790
Milekic MH, Xin Y, O'Donnell A, Kumar KK, Bradley-Moore M, Malaspina D, et al. Age-related sperm DNA methylation changes are transmitted to offspring and associated with abnormal behavior and dysregulated gene expression. Mol Psychiatry. 2015;20(8):995–1001. https://doi.org/10.1038/mp.2014.84 .
doi: 10.1038/mp.2014.84
pubmed: 25092244
Denomme MM, Haywood ME, Parks JC, Schoolcraft WB, Katz-Jaffe MG. The inherited methylome landscape is directly altered with paternal aging and associated with offspring neurodevelopmental disorders. Aging Cell. 2020:e13178. https://doi.org/10.1111/acel.13178 .