Regulation with cell size ensures mitochondrial DNA homeostasis during cell growth.


Journal

Nature structural & molecular biology
ISSN: 1545-9985
Titre abrégé: Nat Struct Mol Biol
Pays: United States
ID NLM: 101186374

Informations de publication

Date de publication:
10 2023
Historique:
received: 18 03 2022
accepted: 07 08 2023
medline: 23 10 2023
pubmed: 8 9 2023
entrez: 7 9 2023
Statut: ppublish

Résumé

To maintain stable DNA concentrations, proliferating cells need to coordinate DNA replication with cell growth. For nuclear DNA, eukaryotic cells achieve this by coupling DNA replication to cell-cycle progression, ensuring that DNA is doubled exactly once per cell cycle. By contrast, mitochondrial DNA replication is typically not strictly coupled to the cell cycle, leaving the open question of how cells maintain the correct amount of mitochondrial DNA during cell growth. Here, we show that in budding yeast, mitochondrial DNA copy number increases with cell volume, both in asynchronously cycling populations and during G1 arrest. Our findings suggest that cell-volume-dependent mitochondrial DNA maintenance is achieved through nuclear-encoded limiting factors, including the mitochondrial DNA polymerase Mip1 and the packaging factor Abf2, whose amount increases in proportion to cell volume. By directly linking mitochondrial DNA maintenance to nuclear protein synthesis and thus cell growth, constant mitochondrial DNA concentrations can be robustly maintained without a need for cell-cycle-dependent regulation.

Identifiants

pubmed: 37679564
doi: 10.1038/s41594-023-01091-8
pii: 10.1038/s41594-023-01091-8
pmc: PMC10584693
doi:

Substances chimiques

DNA, Mitochondrial 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1549-1560

Informations de copyright

© 2023. The Author(s).

Références

Sclafani, R. A. & Holzen, T. M. Cell cycle regulation of DNA replication. Annu. Rev. Genet. 41, 237–280 (2007).
pubmed: 17630848 pmcid: 2292467 doi: 10.1146/annurev.genet.41.110306.130308
Ekundayo, B. & Bleichert, F. Origins of DNA replication. PLoS Genet. 15, e1008320 (2019).
pubmed: 31513569 pmcid: 6742236 doi: 10.1371/journal.pgen.1008320
Gustafsson, C. M., Falkenberg, M. & Larsson, N.-G. Maintenance and expression of mammalian mitochondrial DNA. Annu. Rev. Biochem. 85, 133–160 (2016).
pubmed: 27023847 doi: 10.1146/annurev-biochem-060815-014402
Aretz, I., Jakubke, C. & Osman, C. Power to the daughters—mitochondrial and mtDNA transmission during cell division. Biol. Chem. 401, 533–546 (2020).
pubmed: 31812944 doi: 10.1515/hsz-2019-0337
Kukat, C. et al. Super-resolution microscopy reveals that mammalian mitochondrial nucleoids have a uniform size and frequently contain a single copy of mtDNA. Proc. Natl Acad. Sci. USA 108, 13534–13539 (2011).
pubmed: 21808029 pmcid: 3158146 doi: 10.1073/pnas.1109263108
Göke, A. et al. Mrx6 regulates mitochondrial DNA copy number in Saccharomyces cerevisiae by engaging the evolutionarily conserved Lon protease Pim1. Mol. Biol. Cell 31, 527–545 (2020).
pubmed: 31532710 pmcid: 7202074 doi: 10.1091/mbc.E19-08-0470
Ekstrand, M. I. et al. Mitochondrial transcription factor A regulates mtDNA copy number in mammals. Hum. Mol. Genet. 13, 935–944 (2004).
pubmed: 15016765 doi: 10.1093/hmg/ddh109
Zelenaya-Troitskaya, O., Newman, S. M., Okamoto, K., Perlman, P. S. & Butow, R. A. Functions of the high mobility group protein, Abf2p, in mitochondrial DNA segregation, recombination and copy number in Saccharomyces cerevisiae. Genetics 148, 1763–1776 (1998).
pubmed: 9581629 pmcid: 1460092 doi: 10.1093/genetics/148.4.1763
Stumpf, J. D. et al. mip1 containing mutations associated with mitochondrial disease causes mutagenesis and depletion of mtDNA in Saccharomyces cerevisiae. Hum. Mol. Genet. 19, 2123–2133 (2010).
pubmed: 20185557 pmcid: 2865372 doi: 10.1093/hmg/ddq089
Tyynismaa, H. et al. Twinkle helicase is essential for mtDNA maintenance and regulates mtDNA copy number. Hum. Mol. Genet. 13, 3219–3227 (2004).
pubmed: 15509589 doi: 10.1093/hmg/ddh342
Taylor, S. D. et al. The conserved Mec1/Rad53 nuclear checkpoint pathway regulates mitochondrial DNA copy number in Saccharomyces cerevisiae. Mol. Biol. Cell 16, 3010–3018 (2005).
pubmed: 15829566 pmcid: 1142443 doi: 10.1091/mbc.e05-01-0053
Lee, S., Kim, S., Sun, X., Lee, J.-H. & Cho, H. Cell cycle-dependent mitochondrial biogenesis and dynamics in mammalian cells. Biochem. Biophys. Res. Commun. 357, 111–117 (2007).
pubmed: 17400185 doi: 10.1016/j.bbrc.2007.03.091
Chatre, L. & Ricchetti, M. Prevalent coordination of mitochondrial DNA transcription and initiation of replication with the cell cycle. Nucleic Acids Res. 41, 3068–3078 (2013).
pubmed: 23345615 pmcid: 3597681 doi: 10.1093/nar/gkt015
Sasaki, T., Sato, Y., Higashiyama, T. & Sasaki, N. Live imaging reveals the dynamics and regulation of mitochondrial nucleoids during the cell cycle in Fucci2-HeLa cells. Sci. Rep. 7, 11257 (2017).
pubmed: 28900194 pmcid: 5595809 doi: 10.1038/s41598-017-10843-8
Petes, T. D. & Fangman, W. L. Preferential synthesis of yeast mitochondrial DNA in alpha factor-arrested cells. Biochem. Biophys. Res. Commun. 55, 603–609 (1973).
pubmed: 4586613 doi: 10.1016/0006-291X(73)91186-8
Wells, J. R. Mitochondrial DNA synthesis during the cell cycle of Saccharomyces cerevisiae. Exp. Cell. Res. 85, 278–286 (1974).
pubmed: 4597335 doi: 10.1016/0014-4827(74)90128-1
Newlon, C. S. & Fangman, W. L. Mitochondrial DNA synthesis in cell cycle mutants of Saccharomyces cerevisiae. Cell 5, 423–428 (1975).
pubmed: 1098780 doi: 10.1016/0092-8674(75)90061-6
Conrad, M. N. & Newlon, C. S. The regulation of mitochondrial DNA levels in Saccharomyces cerevisiae. Curr. Genet. 6, 147–152 (1982).
pubmed: 24186481 doi: 10.1007/BF00435214
Rafelski, S. M. et al. Mitochondrial network size scaling in budding yeast. Science 338, 822–824 (2012).
pubmed: 23139336 pmcid: 3602416 doi: 10.1126/science.1225720
Posakony, J., England, J. & Attardi, G. Mitochondrial growth and division during the cell cycle in HeLa cells. J. Cell Biol. 74, 468–491 (1977).
pubmed: 885911 pmcid: 2110063 doi: 10.1083/jcb.74.2.468
Miettinen, T. P. et al. Identification of transcriptional and metabolic programs related to mammalian cell size. Curr. Biol. 24, 598–608 (2014).
pubmed: 24613310 pmcid: 3991852 doi: 10.1016/j.cub.2014.01.071
Miettinen, T. P. & Björklund, M. Cellular allometry of mitochondrial functionality establishes the optimal cell size. Dev. Cell 39, 370–382 (2016).
pubmed: 27720611 pmcid: 5104693 doi: 10.1016/j.devcel.2016.09.004
Osman, C., Noriega, T. R., Okreglak, V., Fung, J. C. & Walter, P. Integrity of the yeast mitochondrial genome, but not its distribution and inheritance, relies on mitochondrial fission and fusion. Proc. Natl Acad. Sci. USA 112, E947–E956 (2015).
pubmed: 25730886 pmcid: 4352819 doi: 10.1073/pnas.1501737112
Jajoo, R. et al. Accurate concentration control of mitochondria and nucleoids. Science 351, 169–172 (2016).
pubmed: 26744405 pmcid: 4823142 doi: 10.1126/science.aaa8714
Ottoz, D. S. M., Rudolf, F. & Stelling, J. Inducible, tightly regulated and growth condition-independent transcription factor in Saccharomyces cerevisiae. Nucleic Acids Res. 42, e130 (2014).
pubmed: 25034689 pmcid: 4176152 doi: 10.1093/nar/gku616
Schmoller, K. M., Turner, J. J., Kõivomägi, M. & Skotheim, J. M. Dilution of the cell cycle inhibitor Whi5 controls budding-yeast cell size. Nature 526, 268–272 (2015).
pubmed: 26390151 pmcid: 4600446 doi: 10.1038/nature14908
Claude, K.-L. et al. Transcription coordinates histone amounts and genome content. Nat. Commun. 12, 4202 (2021).
pubmed: 34244507 pmcid: 8270936 doi: 10.1038/s41467-021-24451-8
Kukhtevich, I. V., Lohrberg, N., Padovani, F., Schneider, R. & Schmoller, K. M. Cell size sets the diameter of the budding yeast contractile ring. Nat. Commun. 11, 2952 (2020).
pubmed: 32528053 pmcid: 7289848 doi: 10.1038/s41467-020-16764-x
Ewald, J. C., Kuehne, A., Zamboni, N. & Skotheim, J. M. The yeast cyclin-dependent kinase routes carbon fluxes to fuel cell cycle progression. Mol. Cell 62, 532–545 (2016).
pubmed: 27203178 pmcid: 4875507 doi: 10.1016/j.molcel.2016.02.017
Padovani, F., Mairhörmann, B., Falter-Braun, P., Lengefeld, J. & Schmoller, K. M. Segmentation, tracking and cell cycle analysis of live-cell imaging data with Cell-ACDC. BMC Biol. 20, 174 (2022).
pubmed: 35932043 pmcid: 9356409 doi: 10.1186/s12915-022-01372-6
Klecker, T. & Westermann, B. Pathways shaping the mitochondrial inner membrane. Open Biol. 11, 210238 (2021).
pubmed: 34847778 pmcid: 8633786 doi: 10.1098/rsob.210238
Jakubke, C. et al. Cristae-dependent quality control of the mitochondrial genome. Sci. Adv. 7, eabi8886 (2021).
pubmed: 34516914 pmcid: 8442932 doi: 10.1126/sciadv.abi8886
Hoppins, S. et al. A mitochondrial-focused genetic interaction map reveals a scaffold-like complex required for inner membrane organization in mitochondria. J. Cell Biol. 195, 323–340 (2011).
pubmed: 21987634 pmcid: 3198156 doi: 10.1083/jcb.201107053
von der Malsburg, K. et al. Dual role of mitofilin in mitochondrial membrane organization and protein biogenesis. Dev. Cell 21, 694–707 (2011).
pubmed: 21944719 doi: 10.1016/j.devcel.2011.08.026
Harner, M. et al. The mitochondrial contact site complex, a determinant of mitochondrial architecture: Molecular architecture of mitochondria. EMBO J. 30, 4356–4370 (2011).
pubmed: 22009199 pmcid: 3230385 doi: 10.1038/emboj.2011.379
Swaffer, M. P. et al. Transcriptional and chromatin-based partitioning mechanisms uncouple protein scaling from cell size. Mol. Cell 81, 4861-4875 (2021).
Marguerat, S. & Bähler, J. Coordinating genome expression with cell size. Trends Genet. 28, 560–565 (2012).
pubmed: 22863032 doi: 10.1016/j.tig.2012.07.003
Schmoller, K. M. & Skotheim, J. M. The biosynthetic basis of cell size control. Trends Cell Biol. 25, 793–802 (2015).
pubmed: 26573465 pmcid: 6773270 doi: 10.1016/j.tcb.2015.10.006
Wu, C.-Y., Rolfe, P. A., Gifford, D. K. & Fink, G. R. Control of transcription by cell size. PLoS Biol. 8, e1000523 (2010).
pubmed: 21072241 pmcid: 2970550 doi: 10.1371/journal.pbio.1000523
Zhurinsky, J. et al. A coordinated global control over cellular transcription. Curr. Biol.: CB 20, 2010–2015 (2010).
pubmed: 20970341 doi: 10.1016/j.cub.2010.10.002
Padovan-Merhar, O. et al. Single mammalian cells compensate for differences in cellular volume and DNA copy number through independent global transcriptional mechanisms. Mol. Cell 58, 339–352 (2015).
pubmed: 25866248 pmcid: 4402149 doi: 10.1016/j.molcel.2015.03.005
Sun, X.-M. et al. Size-dependent increase in RNA polymerase II initiation rates mediates gene expression scaling with cell size. Curr. Biol. 30, 1217–1230 (2020).
pubmed: 32059768 doi: 10.1016/j.cub.2020.01.053
Swaffer, M. P. et al. RNA polymerase II dynamics and mRNA stability feedback determine mRNA scaling with cell size. Preprint at bioRxiv https://doi.org/10.1101/2021.09.20.461005 (2022).
Parts, L. et al. Heritability and genetic basis of protein level variation in an outbred population. Genome Res. 24, 1363–1370 (2014).
pubmed: 24823668 pmcid: 4120089 doi: 10.1101/gr.170506.113
Contamine, V. & Picard, M. Maintenance and integrity of the mitochondrial genome: a plethora of nuclear genes in the budding yeast. Microbiol. Mol. Biol. Rev. 64, 281–315 (2000).
pubmed: 10839818 pmcid: 98995 doi: 10.1128/MMBR.64.2.281-315.2000
Van Dyck, E., Foury, F., Stillman, B. & Brill, S. J. A single-stranded DNA binding protein required for mitochondrial DNA replication in S. cerevisiae is homologous to E. coli SSB. EMBO J. 11, 3421–3430 (1992).
pubmed: 1324172 pmcid: 556877 doi: 10.1002/j.1460-2075.1992.tb05421.x
Crider, D. G. et al. Rad53 is essential for a mitochondrial DNA inheritance checkpoint regulating G1 to S progression. J. Cell Biol. 198, 793–798 (2012).
pubmed: 22927468 pmcid: 3432762 doi: 10.1083/jcb.201205193
Muellner, J. & Schmidt, K. H. Yeast genome maintenance by the multifunctional PIF1 DNA helicase family. Genes 11, 224 (2020).
pubmed: 32093266 pmcid: 7073672 doi: 10.3390/genes11020224
Sedman, T., Kuusk, S., Kivi, S. & Sedman, J. A DNA helicase required for maintenance of the functional mitochondrial genome in Saccharomyces cerevisiae. Mol. Cell. Biol. 20, 1816–1824 (2000).
pubmed: 10669756 pmcid: 85362 doi: 10.1128/MCB.20.5.1816-1824.2000
Ling, F. & Yoshida, M. Rolling-circle replication in mitochondrial DNA inheritance: scientific evidence and significance from yeast to human cells. Genes 11, 514 (2020).
pubmed: 32384722 pmcid: 7288456 doi: 10.3390/genes11050514
Torres, E. M., Springer, M. & Amon, A. No current evidence for widespread dosage compensation in S. cerevisiae. eLife 5, e10996 (2016).
pubmed: 26949255 pmcid: 4798953 doi: 10.7554/eLife.10996
Springer, M., Weissman, J. S. & Kirschner, M. W. A general lack of compensation for gene dosage in yeast. Mol. Syst. Biol. 6, 368 (2010).
pubmed: 20461075 pmcid: 2890323 doi: 10.1038/msb.2010.19
Viikov, K., Jasnovidova, O., Tamm, T. & Sedman, J. C-terminal extension of the yeast mitochondrial DNA polymerase determines the balance between synthesis and degradation. PLoS ONE 7, e33482 (2012).
pubmed: 22432028 pmcid: 3303844 doi: 10.1371/journal.pone.0033482
Diffley, J. F. & Stillman, B. A close relative of the nuclear, chromosomal high-mobility group protein HMG1 in yeast mitochondria. Proc. Natl Acad. Sci. USA 88, 7864–7868 (1991).
pubmed: 1881919 pmcid: 52404 doi: 10.1073/pnas.88.17.7864
Lee, E. & Johnson, B. F. Volume-related mitochondrial deoxyribonucleic acid synthesis in zygotes and vegetative cells of Saccharomyces cerevisiae. J. Bacteriol. 129, 1066–1071 (1977).
pubmed: 320176 pmcid: 235047 doi: 10.1128/jb.129.2.1066-1071.1977
Woodward, R. & Gull, K. Timing of nuclear and kinetoplast DNA replication and early morphological events in the cell cycle of Trypanosoma brucei. J. Cell Sci. 95, 49–57 (1990).
pubmed: 2190996 doi: 10.1242/jcs.95.1.49
Santos, A., Wernersson, R. & Jensen, L. J. Cyclebase 3.0: a multi-organism database on cell-cycle regulation and phenotypes. Nucleic Acids Res. 43, D1140–D1144 (2015).
pubmed: 25378319 doi: 10.1093/nar/gku1092
Larsson, N.-G. et al. Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice. Nat. Genet. 18, 231–236 (1998).
pubmed: 9500544 doi: 10.1038/ng0398-231
Matsushima, Y. et al. Functional domains of chicken mitochondrial transcription factor A for the maintenance of mitochondrial DNA copy number in lymphoma cell line DT40. J. Biol. Chem. 278, 31149–31158 (2003).
pubmed: 12759347 doi: 10.1074/jbc.M303842200
Lanz, M. C. et al. Increasing cell size remodels the proteome and promotes senescence. Mol. Cell 82, P3255–3269.e8 (2022).
doi: 10.1016/j.molcel.2022.07.017
Stringer, C., Wang, T., Michaelos, M. & Pachitariu, M. Cellpose: a generalist algorithm for cellular segmentation. Nat. Methods 18, 100–106 (2021).
pubmed: 33318659 doi: 10.1038/s41592-020-01018-x
Li, C. H. & Tam, P. K. S. An iterative algorithm for minimum cross entropy thresholding. Pattern Recognit. Lett. 19, 771–776 (1998).
doi: 10.1016/S0167-8655(98)00057-9
van der Walt, S. et al. scikit-image: image processing in Python. PeerJ 2, e453 (2014).
pubmed: 25024921 pmcid: 4081273 doi: 10.7717/peerj.453
Lee, T. C., Kashyap, R. L. & Chu, C. N. Building skeleton models via 3-D medial surface axis thinning algorithms. CVGIP Graph. Models Image Process. 56, 462–478 (1994).
doi: 10.1006/cgip.1994.1042
Miyakawa, I., Miyamoto, M., Kuroiwa, T. & Sando, N. DNA content of individual mitochondrial nucleoids varies depending on the culture conditions of the yeast Saccharomyces cerevisiae. Cytologia 69, 101–107 (2004).
doi: 10.1508/cytologia.69.101
Viana, M. P., Lim, S. & Rafelski, S. M. in Methods in Cell Biology 77–93 (Elsevier, 2015).
Perkins, E. M. & McCaffery, J. M. in Mitochondria Methods in Molecular Biology (eds Leister, D. & Herrmann, J. M.) 467–483 (Humana Press, 2007).
Unger, A.-K. et al. (2017). in Mitochondria Methods in Molecular Biology (eds Mokranjac, D. & Perocchi, F.) 293–314 (Springer New York, 2017).
Schindelin, J. et al. Fiji: an open-source platform for biological-image analysis. Nat. Methods 9, 676–682 (2012).
pubmed: 22743772 doi: 10.1038/nmeth.2019
Ghaemmaghami, S. et al. Global analysis of protein expression in yeast. Nature 425, 737–741 (2003).
pubmed: 14562106 doi: 10.1038/nature02046

Auteurs

Anika Seel (A)

Institute of Functional Epigenetics, Molecular Targets and Therapeutics Center, Helmholtz Zentrum München, Neuherberg, Germany.

Francesco Padovani (F)

Institute of Functional Epigenetics, Molecular Targets and Therapeutics Center, Helmholtz Zentrum München, Neuherberg, Germany.

Moritz Mayer (M)

Institute of Cell Biology, University of Bayreuth, Bayreuth, Germany.

Alissa Finster (A)

Institute of Functional Epigenetics, Molecular Targets and Therapeutics Center, Helmholtz Zentrum München, Neuherberg, Germany.

Daniela Bureik (D)

Institute of Functional Epigenetics, Molecular Targets and Therapeutics Center, Helmholtz Zentrum München, Neuherberg, Germany.

Felix Thoma (F)

Faculty of Biology, Ludwig-Maximilians-Universität München, Planegg-Martinsried, Germany.

Christof Osman (C)

Faculty of Biology, Ludwig-Maximilians-Universität München, Planegg-Martinsried, Germany.

Till Klecker (T)

Institute of Cell Biology, University of Bayreuth, Bayreuth, Germany.

Kurt M Schmoller (KM)

Institute of Functional Epigenetics, Molecular Targets and Therapeutics Center, Helmholtz Zentrum München, Neuherberg, Germany. kurt.schmoller@helmholtz-munich.de.

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