Whole exome sequencing analysis of 167 men with primary infertility.

Azoospermia Male infertility Spermatogenesis Spermatogenic failure Whole exome sequencing

Journal

BMC medical genomics
ISSN: 1755-8794
Titre abrégé: BMC Med Genomics
Pays: England
ID NLM: 101319628

Informations de publication

Date de publication:
12 Sep 2024
Historique:
received: 28 06 2024
accepted: 04 09 2024
medline: 13 9 2024
pubmed: 13 9 2024
entrez: 12 9 2024
Statut: epublish

Résumé

Spermatogenic failure is one of the leading causes of male infertility and its genetic etiology has not yet been fully understood. The study screened a cohort of patients (n = 167) with primary male infertility in contrast to 210 normally fertile men using whole exome sequencing (WES). The expression analysis of the candidate genes based on public single cell sequencing data was performed using the R language Seurat package. No pathogenic copy number variations (CNVs) related to male infertility were identified using the the GATK-gCNV tool. Accordingly, variants of 17 known causative (five X-linked and twelve autosomal) genes, including ACTRT1, ADAD2, AR, BCORL1, CFAP47, CFAP54, DNAH17, DNAH6, DNAH7, DNAH8, DNAH9, FSIP2, MSH4, SLC9C1, TDRD9, TTC21A, and WNK3, were identified in 23 patients. Variants of 12 candidate (seven X-linked and five autosomal) genes were identified, among which CHTF18, DDB1, DNAH12, FANCB, GALNT3, OPHN1, SCML2, UPF3A, and ZMYM3 had altered fertility and semen characteristics in previously described knockout mouse models, whereas MAGEC1,RBMXL3, and ZNF185 were recurrently detected in patients with male factor infertility. The human testis single cell-sequencing database reveals that CHTF18, DDB1 and MAGEC1 are preferentially expressed in spermatogonial stem cells. DNAH12 and GALNT3 are found primarily in spermatocytes and early spermatids. UPF3A is present at a high level throughout spermatogenesis except in elongating spermatids. The testicular expression profiles of these candidate genes underlie their potential roles in spermatogenesis and the pathogenesis of male infertility. WES is an effective tool in the genetic diagnosis of primary male infertility. Our findings provide useful information on precise treatment, genetic counseling, and birth defect prevention for male factor infertility.

Sections du résumé

BACKGROUND BACKGROUND
Spermatogenic failure is one of the leading causes of male infertility and its genetic etiology has not yet been fully understood.
METHODS METHODS
The study screened a cohort of patients (n = 167) with primary male infertility in contrast to 210 normally fertile men using whole exome sequencing (WES). The expression analysis of the candidate genes based on public single cell sequencing data was performed using the R language Seurat package.
RESULTS RESULTS
No pathogenic copy number variations (CNVs) related to male infertility were identified using the the GATK-gCNV tool. Accordingly, variants of 17 known causative (five X-linked and twelve autosomal) genes, including ACTRT1, ADAD2, AR, BCORL1, CFAP47, CFAP54, DNAH17, DNAH6, DNAH7, DNAH8, DNAH9, FSIP2, MSH4, SLC9C1, TDRD9, TTC21A, and WNK3, were identified in 23 patients. Variants of 12 candidate (seven X-linked and five autosomal) genes were identified, among which CHTF18, DDB1, DNAH12, FANCB, GALNT3, OPHN1, SCML2, UPF3A, and ZMYM3 had altered fertility and semen characteristics in previously described knockout mouse models, whereas MAGEC1,RBMXL3, and ZNF185 were recurrently detected in patients with male factor infertility. The human testis single cell-sequencing database reveals that CHTF18, DDB1 and MAGEC1 are preferentially expressed in spermatogonial stem cells. DNAH12 and GALNT3 are found primarily in spermatocytes and early spermatids. UPF3A is present at a high level throughout spermatogenesis except in elongating spermatids. The testicular expression profiles of these candidate genes underlie their potential roles in spermatogenesis and the pathogenesis of male infertility.
CONCLUSION CONCLUSIONS
WES is an effective tool in the genetic diagnosis of primary male infertility. Our findings provide useful information on precise treatment, genetic counseling, and birth defect prevention for male factor infertility.

Identifiants

pubmed: 39267058
doi: 10.1186/s12920-024-02005-3
pii: 10.1186/s12920-024-02005-3
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

230

Subventions

Organisme : Natural Science Foundation of Hunan Province
ID : 2022JJ30322

Informations de copyright

© 2024. The Author(s).

Références

Agarwal A, Baskaran S, Parekh N, Cho CL, Henkel R, Vij S, et al. Male infertility. Lancet. 2021;397(10271):319–33.
pubmed: 33308486 doi: 10.1016/S0140-6736(20)32667-2
Minhas S, Bettocchi C, Boeri L, Capogrosso P, Carvalho J, Cilesiz NC, et al. European Association of Urology Guidelines on male sexual and Reproductive Health: 2021 update on male infertility. Eur Urol. 2021;80(5):603–20.
pubmed: 34511305 doi: 10.1016/j.eururo.2021.08.014
Cham TC, Chen X, Honaramooz A. Current progress, challenges, and future prospects of testis organoidsdagger. Biol Reprod. 2021;104(5):942–61.
pubmed: 33550399 doi: 10.1093/biolre/ioab014
Houston BJ, Riera-Escamilla A, Wyrwoll MJ, Salas-Huetos A, Xavier MJ, Nagirnaja L, et al. A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene-disease relationships. Hum Reprod Update. 2021;28(1):15–29.
pubmed: 34498060 pmcid: 8730311 doi: 10.1093/humupd/dmab030
Nagirnaja L, Lopes AM, Charng WL, Miller B, Stakaitis R, Golubickaite I, et al. Diverse monogenic subforms of human spermatogenic failure. Nat Commun. 2022;13(1):7953.
pubmed: 36572685 pmcid: 9792524 doi: 10.1038/s41467-022-35661-z
Krausz C, Riera-Escamilla A. Genetics of male infertility. Nat Rev Urol. 2018;15(6):369–84.
pubmed: 29622783 doi: 10.1038/s41585-018-0003-3
Malcher A, Stokowy T, Berman A, Olszewska M, Jedrzejczak P, Sielski D, et al. Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia. Andrology. 2022;10(8):1605–24.
pubmed: 36017582 pmcid: 9826517 doi: 10.1111/andr.13269
Hermann BP, Cheng K, Singh A, Roa-De La Cruz L, Mutoji KN, Chen IC, et al. The mammalian spermatogenesis single-cell transcriptome, from Spermatogonial Stem cells to Spermatids. Cell Rep. 2018;25(6):1650–e16671658.
pubmed: 30404016 pmcid: 6384825 doi: 10.1016/j.celrep.2018.10.026
Babadi M, Fu JM, Lee SK, Smirnov AN, Gauthier LD, Walker M, et al. GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data. Nat Genet. 2023;55(9):1589–97.
pubmed: 37604963 pmcid: 10904014 doi: 10.1038/s41588-023-01449-0
Sha Y, Liu W, Li L, Serafimovski M, Isachenko V, Li Y, et al. Pathogenic variants in ACTRT1 cause Acephalic Spermatozoa Syndrome. Front Cell Dev Biol. 2021;9:676246.
pubmed: 34422805 pmcid: 8377740 doi: 10.3389/fcell.2021.676246
Dai S, Liu M, Liu M, Jiang C, Yang Y, Han H, et al. Population-based genetic analysis in infertile men reveals novel mutations of ADAD family members in patients with impaired spermatogenesis. Hum Mol Genet. 2023;32(11):1814–25.
pubmed: 36708028 doi: 10.1093/hmg/ddad012
Giwercman YL, Nikoshkov A, Bystrom B, Pousette A, Arver S, Wedell A. A novel mutation (N233K) in the transactivating domain and the N756S mutation in the ligand binding domain of the androgen receptor gene are associated with male infertility. Clin Endocrinol (Oxf). 2001;54(6):827–34.
pubmed: 11422119 doi: 10.1046/j.1365-2265.2001.01308.x
Lu C, Zhang Y, Qin Y, Xu Q, Zhou R, Cui Y, et al. Human X chromosome exome sequencing identifies BCORL1 as contributor to spermatogenesis. J Med Genet. 2021;58(1):56–65.
pubmed: 32376790 doi: 10.1136/jmedgenet-2019-106598
Liu C, Tu C, Wang L, Wu H, Houston BJ, Mastrorosa FK, et al. Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility. Am J Hum Genet. 2021;108(2):309–23.
pubmed: 33472045 pmcid: 7895902 doi: 10.1016/j.ajhg.2021.01.002
Whitfield M, Thomas L, Bequignon E, Schmitt A, Stouvenel L, Montantin G, et al. Mutations in DNAH17, encoding a sperm-specific axonemal outer Dynein Arm Heavy Chain, cause isolated male infertility due to Asthenozoospermia. Am J Hum Genet. 2019;105(1):198–212.
pubmed: 31178125 pmcid: 6612517 doi: 10.1016/j.ajhg.2019.04.015
Tu C, Nie H, Meng L, Yuan S, He W, Luo A, et al. Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella. Sci Rep. 2019;9(1):15864.
pubmed: 31676830 pmcid: 6825154 doi: 10.1038/s41598-019-52436-7
Wei X, Sha Y, Wei Z, Zhu X, He F, Zhang X, et al. Bi-allelic mutations in DNAH7 cause asthenozoospermia by impairing the integrality of axoneme structure. Acta Biochim Biophys Sin (Shanghai). 2021;53(10):1300–9.
pubmed: 34476482 doi: 10.1093/abbs/gmab113
Liu C, Miyata H, Gao Y, Sha Y, Tang S, Xu Z, et al. Bi-allelic DNAH8 variants lead to multiple morphological abnormalities of the sperm flagella and primary male infertility. Am J Hum Genet. 2020;107(2):330–41.
pubmed: 32619401 pmcid: 7413861 doi: 10.1016/j.ajhg.2020.06.004
Tang D, Sha Y, Gao Y, Zhang J, Cheng H, Zhang J, et al. Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia. Reprod Biol Endocrinol. 2021;19(1):27.
pubmed: 33610189 pmcid: 7896388 doi: 10.1186/s12958-021-00709-0
Martinez G, Kherraf ZE, Zouari R, Fourati Ben Mustapha S, Saut A, Pernet-Gallay K, et al. Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella. Hum Reprod. 2018;33(10):1973–84.
pubmed: 30137358 doi: 10.1093/humrep/dey264
Wyrwoll MJ, van Walree ES, Hamer G, Rotte N, Motazacker MM, Meijers-Heijboer H, et al. Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes. Hum Reprod. 2021;37(1):178–89.
pubmed: 34755185 doi: 10.1093/humrep/deab230
Cavarocchi E, Whitfield M, Chargui A, Stouvenel L, Lores P, Coutton C, et al. The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility. Clin Genet. 2021;99(5):684–93.
pubmed: 33462806 doi: 10.1111/cge.13927
Arafat M, Har-Vardi I, Harlev A, Levitas E, Zeadna A, Abofoul-Azab M, et al. Mutation in TDRD9 causes non-obstructive azoospermia in infertile men. J Med Genet. 2017;54(9):633–9.
pubmed: 28536242 doi: 10.1136/jmedgenet-2017-104514
Liu W, He X, Yang S, Zouari R, Wang J, Wu H, et al. Bi-allelic mutations in TTC21A induce asthenoteratospermia in humans and mice. Am J Hum Genet. 2019;104(4):738–48.
pubmed: 30929735 pmcid: 6451729 doi: 10.1016/j.ajhg.2019.02.020
Fakhro KA, Elbardisi H, Arafa M, Robay A, Rodriguez-Flores JL, Al-Shakaki A, et al. Point-of-care whole-exome sequencing of idiopathic male infertility. Genet Med. 2018;20(11):1365–73.
pubmed: 29790874 doi: 10.1038/gim.2018.10
Tian S, Tu C, He X, Meng L, Wang J, Tang S, et al. Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA. J Med Genet. 2023;60(8):827–34.
pubmed: 36593121 doi: 10.1136/jmg-2022-108887
Berkowitz KM, Sowash AR, Koenig LR, Urcuyo D, Khan F, Yang F, et al. Disruption of CHTF18 causes defective meiotic recombination in male mice. PLoS Genet. 2012;8(11):e1002996.
pubmed: 23133398 pmcid: 3486840 doi: 10.1371/journal.pgen.1002996
Zheng W, Nazish J, Wahab F, Khan R, Jiang X, Shi Q. DDB1 regulates sertoli cell proliferation and testis cord remodeling by TGFbeta Pathway. Genes (Basel) 2019, 10(12).
Li Y, Wang Y, Wen Y, Zhang T, Wang X, Jiang C, et al. Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects. Hum Reprod. 2021;37(1):152–77.
pubmed: 34791246 doi: 10.1093/humrep/deab229
Geng H, Wang K, Liang D, Ni X, Yu H, Tang D, et al. Further evidence from DNAH12 supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variants. iScience. 2024;27(7):110366.
pubmed: 39071892 pmcid: 11278020 doi: 10.1016/j.isci.2024.110366
Oud MS, Houston BJ, Volozonoka L, Mastrorosa FK, Holt GS, Alobaidi BKS, et al. Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders. Hum Reprod. 2021;36(9):2597–611.
pubmed: 34089056 pmcid: 8373475 doi: 10.1093/humrep/deab099
Kato Y, Alavattam KG, Sin HS, Meetei AR, Pang Q, Andreassen PR, et al. FANCB is essential in the male germline and regulates H3K9 methylation on the sex chromosomes during meiosis. Hum Mol Genet. 2015;24(18):5234–49.
pubmed: 26123487 pmcid: 4550819 doi: 10.1093/hmg/ddv244
Miyazaki T, Mori M, Yoshida CA, Ito C, Yamatoya K, Moriishi T, et al. Galnt3 deficiency disrupts acrosome formation and leads to oligoasthenoteratozoospermia. Histochem Cell Biol. 2013;139(2):339–54.
pubmed: 23052838 doi: 10.1007/s00418-012-1031-3
Sakashita A, Ooga M, Otsuka K, Maezawa S, Takeuchi C, Wakayama S, et al. Polycomb protein SCML2 mediates paternal epigenetic inheritance through sperm chromatin. Nucleic Acids Res. 2023;51(13):6668–83.
pubmed: 37283086 pmcid: 10359620 doi: 10.1093/nar/gkad479
Shum EY, Jones SH, Shao A, Chousal JN, Krause MD, Chan WK, et al. The antagonistic gene paralogs Upf3a and Upf3b govern nonsense-mediated RNA decay. Cell. 2016;165(2):382–95.
pubmed: 27040500 pmcid: 4826573 doi: 10.1016/j.cell.2016.02.046
Hu X, Shen B, Liao S, Ning Y, Ma L, Chen J, et al. Gene knockout of Zmym3 in mice arrests spermatogenesis at meiotic metaphase with defects in spindle assembly checkpoint. Cell Death Dis. 2017;8(6):e2910.
pubmed: 28661483 pmcid: 5520888 doi: 10.1038/cddis.2017.228
Krausz C, Riera-Escamilla A, Moreno-Mendoza D, Holleman K, Cioppi F, Algaba F, et al. Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men. Genet Med. 2020;22(12):1956–66.
pubmed: 32741963 pmcid: 7710580 doi: 10.1038/s41436-020-0907-1
Chen S, Wang G, Zheng X, Ge S, Dai Y, Ping P, et al. Whole-exome sequencing of a large Chinese azoospermia and severe oligospermia cohort identifies novel infertility causative variants and genes. Hum Mol Genet. 2020;29(14):2451–9.
pubmed: 32469048 doi: 10.1093/hmg/ddaa101
Tang D, Li K, Geng H, Xu C, Lv M, Gao Y, et al. Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia. Reprod Biol Endocrinol. 2022;20(1):63.
pubmed: 35366911 pmcid: 8976310 doi: 10.1186/s12958-022-00936-z
Zhang H, Li W, Jiang Y, Li J, Chen M, Wang R, et al. Whole exome sequencing identifies genes Associated with Non-obstructive Azoospermia. Front Genet. 2022;13:872179.
pubmed: 35495142 pmcid: 9043847 doi: 10.3389/fgene.2022.872179
Kherraf ZE, Cazin C, Bouker A, Fourati Ben Mustapha S, Hennebicq S, Septier A, et al. Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia. Am J Hum Genet. 2022;109(3):508–17.
pubmed: 35172124 pmcid: 8948161 doi: 10.1016/j.ajhg.2022.01.011
Lillepea K, Juchnewitsch AG, Kasak L, Valkna A, Dutta A, Pomm K, et al. Toward clinical exomes in diagnostics and management of male infertility. Am J Hum Genet. 2024;111(5):877–95.
pubmed: 38614076 doi: 10.1016/j.ajhg.2024.03.013
Li P, Ji Z, Zhi E, Zhang Y, Han S, Zhao L, et al. Novel bi-allelic MSH4 variants causes meiotic arrest and non-obstructive azoospermia. Reprod Biol Endocrinol. 2022;20(1):21.
pubmed: 35090489 pmcid: 8796546 doi: 10.1186/s12958-022-00900-x
Yuan Y, Xu WQ, Chen Y, Luo T, Chen HY. A Gly684Ala substitution in the androgen receptor is the cause for azoospermia in a Chinese family with mild androgen insensitivity syndrome and normal hormone levels. Front Genet. 2022;13:988202.
pubmed: 36159980 pmcid: 9500528 doi: 10.3389/fgene.2022.988202
Smith LB, Walker WH. The regulation of spermatogenesis by androgens. Semin Cell Dev Biol. 2014;30:2–13.
pubmed: 24598768 doi: 10.1016/j.semcdb.2014.02.012
Neyton S, Lespinasse F, Moens PB, Paul R, Gaudray P, Paquis-Flucklinger V, et al. Association between MSH4 (MutS homologue 4) and the DNA strand-exchange RAD51 and DMC1 proteins during mammalian meiosis. Mol Hum Reprod. 2004;10(12):917–24.
pubmed: 15489243 doi: 10.1093/molehr/gah123
Shoji M, Tanaka T, Hosokawa M, Reuter M, Stark A, Kato Y, et al. The TDRD9-MIWI2 complex is essential for piRNA-mediated retrotransposon silencing in the mouse male germline. Dev Cell. 2009;17(6):775–87.
pubmed: 20059948 doi: 10.1016/j.devcel.2009.10.012
Silvanovich A, Li MG, Serr M, Mische S, Hays TS. The third P-loop domain in cytoplasmic dynein heavy chain is essential for dynein motor function and ATP-sensitive microtubule binding. Mol Biol Cell. 2003;14(4):1355–65.
pubmed: 12686593 pmcid: 153106 doi: 10.1091/mbc.e02-10-0675
Inaba K, Mizuno K. Sperm dysfunction and ciliopathy. Reprod Med Biol. 2016;15(2):77–94.
pubmed: 29259424 doi: 10.1007/s12522-015-0225-5
Muranishi Y, Kobori Y, Katoh-Fukui Y, Tamaoka S, Hattori A, Osaka A, et al. Systematic molecular analyses for 115 karyotypically normal men with isolated non-obstructive azoospermia. Hum Reprod. 2024;39(5):1131–40.
pubmed: 38511217 doi: 10.1093/humrep/deae057
Gershoni M, Hauser R, Yogev L, Lehavi O, Azem F, Yavetz H, et al. A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes. Genet Med. 2017;19(9):998–1006.
pubmed: 28206990 doi: 10.1038/gim.2016.225

Auteurs

Haiyan Zhou (H)

National Health Commission Key Laboratory of Birth Defects for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, 410008, China.

Zhaochu Yin (Z)

National Health Commission Key Laboratory of Birth Defects for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, 410008, China.

Bin Ni (B)

National Health Commission Key Laboratory of Birth Defects for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, 410008, China.

Jiwu Lin (J)

National Health Commission Key Laboratory of Birth Defects for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, 410008, China.

Shuwei Luo (S)

Center for Reproductive Medicine, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, 410008, China. luobosing@gmail.com.
Hunan Provincial Maternal and Child Health Care Hospital, No. 53 Xiangchun Road, Changsha, Hunan, 410008, China. luobosing@gmail.com.

Wanqin Xie (W)

National Health Commission Key Laboratory of Birth Defects for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, 410008, China. wanqinxie@126.com.
Hunan Provincial Maternal and Child Health Care Hospital, No. 53 Xiangchun Road, Changsha, Hunan, 410008, China. wanqinxie@126.com.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH