Role of Polycomb Group Protein Cbx2/M33 in Meiosis Onset and Maintenance of Chromosome Stability in the Mammalian Germline

Genes - Tập 2 Số 1 - Trang 59-80
Claudia Baumann1,2, Rabindranath De La Fuente1,2
1Department of Physiology and Pharmacology, College of Veterinary Medicine, University of Georgia, 501 D.W. Brooks Drive, Athens, GA 30602, USA
2Female Germ Cell Biology Group, Department of Clinical Studies, Center for Animal Transgenesis and Germ Cell Research, School of Veterinary Medicine, University of Pennsylvania, New Bolton Center, 382 West Street Road, Kennett Square, PA, 19348, USA

Tóm tắt

Polycomb group proteins (PcG) are major epigenetic regulators, essential for establishing heritable expression patterns of developmental control genes. The mouse PcG family member M33/Cbx2 (Chromobox homolog protein 2) is a component of the Polycomb-Repressive Complex 1 (PRC1). Targeted deletion of Cbx2/M33 in mice results in homeotic transformations of the axial skeleton, growth retardation and male-to-female sex reversal. In this study, we tested whether Cbx2 is involved in the control of chromatin remodeling processes during meiosis. Our analysis revealed sex reversal in 28.6% of XY−/− embryos, in which a hypoplastic testis and a contralateral ovary were observed in close proximity to the kidney, while the remaining male mutant fetuses exhibited bilateral testicular hypoplasia. Notably, germ cells recovered from Cbx2(XY−/−) testes on day 18.5 of fetal development exhibited premature meiosis onset with synaptonemal complex formation suggesting a role for Cbx2 in the control of meiotic entry in male germ cells. Mutant females exhibited small ovaries with significant germ cell loss and a high proportion of oocytes with abnormal synapsis and non-homologous interactions at the pachytene stage as well as formation of univalents at diplotene. These defects were associated with failure to resolve DNA double strand breaks marked by persistent gH2AX and Rad51 foci at the late pachytene stage. Importantly, two factors required for meiotic silencing of asynapsed chromatin, ubiquitinated histone H2A (ubH2A) and the chromatin remodeling protein BRCA1, co-localized with fully synapsed chromosome axes in the majority of Cbx2(−/−) oocytes. These results provide novel evidence that Cbx2 plays a critical and previously unrecognized role in germ cell viability, meiosis onset and homologous chromosome synapsis in the mammalian germline.

Từ khóa


Tài liệu tham khảo

McLaren, 2003, Primordial germ cells in the mouse, Dev. Biol., 262, 1, 10.1016/S0012-1606(03)00214-8

Baltus, 2006, In germ cells of mouse embryonic ovaries, the decision to enter meiosis precedes premeiotic DNA replication, Nat. Genet., 38, 1430, 10.1038/ng1919

Bowles, 2006, Retinoid signaling determines germ cell fate in mice, Science, 312, 596, 10.1126/science.1125691

Koubova, 2006, Retinoic acid regulates sex-specific timing of meiotic initiation in mice, Proc. Natl. Acad. Sci. USA, 103, 2474, 10.1073/pnas.0510813103

Lin, 2008, Germ Cell-Intrinsic and -Extrinsic Factors Govern Meiotic Initiation in Mouse Embryos, Science, 322, 1685, 10.1126/science.1166340

Bowles, 2007, Retinoic acid, meiosis and germ cell fate in mammals, Development, 134, 3401, 10.1242/dev.001107

Wang, 2010, Epigenetic status determines germ cell meiotic commitment in embryonic and postnatal mammalian gonads, Cell Cycle, 9, 339, 10.4161/cc.9.2.10447

Ohinata, 2005, Blimp1 is a critical determinant of the germ cell lineage in mice, Nature, 436, 207, 10.1038/nature03813

Ohinata, Y., Seki, Y., Payer, B., O'Carroll, D., Surani, M.A., and Saitou, M. (2006). Germline recruitment in mice: a genetic program for epigenetic reprogramming. Ernst Schering Res. Found. Workshop, 143–174.

Ancelin, 2006, Blimp1 associates with Prmt5 and directs histone arginine methylation in mouse germ cells, Nat. Cell Biol., 8, 623, 10.1038/ncb1413

Hajkova, 2008, Chromatin dynamics during epigenetic reprogramming in the mouse germ line, Nature, 452, 877, 10.1038/nature06714

Hayashi, 2005, A histone H3 methyltransferase controls epigenetic events required for meiotic prophase, Nature, 438, 374, 10.1038/nature04112

Matsui, 2007, Epigenetic regulation for the induction of meiosis, Cell Mol. Life Sci., 64, 257, 10.1007/s00018-006-6281-6

Surani, 2007, Genetic and epigenetic regulators of pluripotency, Cell, 128, 747, 10.1016/j.cell.2007.02.010

Peters, 2001, Loss of the Suv39h histone methyltransferases impairs mammalian heterochromatin and genome stability, Cell, 107, 323, 10.1016/S0092-8674(01)00542-6

Tachibana, 2007, Functional dynamics of H3K9 methylation during meiotic prophase progression, Embo J., 26, 3346, 10.1038/sj.emboj.7601767

Bracken, 2009, Polycomb group proteins: navigators of lineage pathways led astray in cancer, Nat. Rev. Cancer, 9, 773, 10.1038/nrc2736

Core, 1997, Altered cellular proliferation and mesoderm patterning in Polycomb-M33-deficient mice, Development, 124, 721, 10.1242/dev.124.3.721

Core, 2000, Altered retinoic acid sensitivity and temporal expression of Hox genes in polycomb-M33-deficient mice, Dev. Biol., 224, 238, 10.1006/dbio.2000.9791

Konrad, 2009, Ovaries and Female Phenotype in a Girl with 46, XY Karyotype and Mutations in the CBX2 Gene, Am. J. Hum. Genet., 84, 658, 10.1016/j.ajhg.2009.03.016

Tsuchiya, 1998, Male-to-female sex reversal in M33 mutant mice, Nature, 393, 688, 10.1038/31482

Munger, 2009, Elucidation of the transcription network governing mammalian sex determination by exploiting strain-specific susceptibility to sex reversal, Genes Dev., 23, 2521, 10.1101/gad.1835809

Core, 2004, Disruption of E2F signaling suppresses the INK4a-induced proliferative defect in M33-deficient mice, Oncogene, 23, 7660, 10.1038/sj.onc.1207998

Eicher, 1982, Mus poschiavinus Y Chromosome in the C57BL/6J Murine Genome Causes Sex Reversal, Science, 217, 535, 10.1126/science.7089579

Baarends, 2005, Silencing of unpaired chromatin and histone H2A ubiquitination in mammalian meiosis, Mol. Cell. Biol., 25, 1041, 10.1128/MCB.25.3.1041-1053.2005

Okada, 2004, Polycomb homologs are involved in teratogenicity of valproic acid in mice, Birth Defects Res. Part A: Clin. Mol. Teratol., 70, 870, 10.1002/bdra.20085

Bernstein, 2006, Mouse polycomb proteins bind differentially to methylated histone H3 and RNA and are enriched in facultative heterochromatin, Mol. Cell. Biol., 26, 2560, 10.1128/MCB.26.7.2560-2569.2006

Vincenz, 2008, Different polycomb group CBX family proteins associate with distinct regions of chromatin using nonhomologous protein sequences, Proc. Natl. Acad. Sci. USA, 105, 16572, 10.1073/pnas.0805317105

Wang, 1997, M33, a mammalian homologue of Drosophila Polycomb localises to euchromatin within interphase nuclei but is enriched within the centromeric heterochromatin of metaphase chromosomes, Cytogenet. Cell Genet., 78, 50, 10.1159/000134626

Mahadevaiah, 2008, Extensive meiotic asynapsis in mice antagonises meiotic silencing of unsynapsed chromatin and consequently disrupts meiotic sex chromosome inactivation, J. Cell Biol., 182, 263, 10.1083/jcb.200710195

Mahadevaiah, 2001, Recombinational DNA double-strand breaks in mice precede synapsis, Nat. Genet., 27, 271, 10.1038/85830

Burgoyne, 2009, The consequences of asynapsis for mammalian meiosis, Nat. Rev. Genet., 10, 207, 10.1038/nrg2505

Wang, 2006, Structural damage to meiotic chromosomes impairs DNA recombination and checkpoint control in mammalian oocytes, J. Cell Biol., 173, 485, 10.1083/jcb.200512077

Schimenti, 2005, Synapsis or silence, Nat. Genet., 37, 11, 10.1038/ng0105-11

Moens, 2002, The time course and chromosomal localization of recombination-related proteins at meiosis in the mouse are compatible with models that can resolve the early DNA-DNA interactions without reciprocal recombination, J. Cell Sci., 115, 1611, 10.1242/jcs.115.8.1611

Bannister, 2004, Homologous recombinational repair proteins in mouse meiosis, Cytogenet. Genome Res., 107, 191, 10.1159/000080597

Turner, 2005, Silencing of unsynapsed meiotic chromosomes in the mouse, Nat. Genet., 37, 41, 10.1038/ng1484

Scheffner, 2010, Regulation of the polycomb protein Ring1B by self-ubiquitination or by E6-AP may have implications to the pathogenesis of Angelman syndrome, Proc. Natl. Acad. Sci. USA, 107, 6788, 10.1073/pnas.1003108107

Fang, 2004, Ring1b-mediated H2A ubiquitination associates with inactive X chromosomes and is involved in initiation of X inactivation, J. Biol. Chem., 279, 52812, 10.1074/jbc.C400493200

Wang, 2004, Role of histone H2A ubiquitination in Polycomb silencing, Nature, 431, 873, 10.1038/nature02985

Cao, 2005, Role of Bmi-1 and Ring1A in H2A Ubiquitylation and Hox Gene Silencing, Mol. Cell, 20, 845, 10.1016/j.molcel.2005.12.002

Mermoud, 2004, Polycomb group proteins Ring1A/B link ubiquitylation of histone H2A to heritable gene silencing and X inactivation, Dev. Cell, 7, 663, 10.1016/j.devcel.2004.10.005

Elderkin, 2007, A Phosphorylated Form of Mel-18 Targets the Ring1B Histone H2A Ubiquitin Ligase to Chromatin, Mol. Cell, 28, 107, 10.1016/j.molcel.2007.08.009

Huen, 2007, RNF8 Transduces the DNA-Damage Signal via Histone Ubiquitylation and Checkpoint Protein Assembly, Cell, 131, 901, 10.1016/j.cell.2007.09.041

Mailand, 2007, RNF8 Ubiquitylates Histones at DNA Double-Strand Breaks and Promotes Assembly of Repair Proteins, Cell, 131, 887, 10.1016/j.cell.2007.09.040

Kouznetsova, 2009, BRCA1-mediated chromatin silencing is limited to oocytes with a small number of asynapsed chromosomes, J. Cell Sci., 122, 2446, 10.1242/jcs.049353

Cherry, 2007, The Mre11 complex influences DNA repair, synapsis, and crossing over in murine meiosis, Curr. Biol., 17, 373, 10.1016/j.cub.2006.12.048

Paul, 2007, Deletion of genes implicated in protecting the integrity of male germ cells has differential effects on the incidence of DNA breaks and germ cell loss, PLoS ONE, 2, e989, 10.1371/journal.pone.0000989

Tarsounas, 1999, Rad51 and Dmc1 Form Mixed Complexes Associated with Mouse Meiotic Chromosome Cores and Synaptonemal Complexes, J. Cell Biol., 147, 207, 10.1083/jcb.147.2.207

Burgoyne, 2007, The management of DNA double-strand breaks in mitotic G(2), and in mammalian meiosis viewed from a mitotic G(2) perspective, Bioessays, 29, 974, 10.1002/bies.20639

Pittman, 1998, Meiotic prophase arrest with failure of chromosome synapsis in mice deficient for Dmc1, a germline-specific RecA homolog, Mol. Cell, 1, 697, 10.1016/S1097-2765(00)80069-6

Yoshida, 1998, The Mouse RecA-like Gene Dmc1 Is Required for Homologous Chromosome Synapsis during Meiosis, Mol. Cell, 1, 707, 10.1016/S1097-2765(00)80070-2

Simon, 2009, Mechanisms of Polycomb gene silencing: knowns and unknowns, Nat. Rev. Mol. Cell. Biol., 10, 697, 10.1038/nrm2763

Muller, 2009, Biochemical mechanisms of gene regulation by polycomb group protein complexes, Curr. Opin. Genet. Dev., 19, 150, 10.1016/j.gde.2009.03.001

Hashimoto, 1998, RAE28, BMI1, and M33 Are Members of Heterogeneous Multimeric Mammalian Polycomb Group Complexes, Biochem. Biophys. Res. Comm., 245, 356, 10.1006/bbrc.1998.8438

Takada, 2007, Mammalian Polycomb Scmh1 mediates exclusion of Polycomb complexes from the XY body in the pachytene spermatocytes, Development, 134, 579, 10.1242/dev.02747

Paro, 1991, The Polycomb protein shares a homologous domain with a heterochromatin-associated protein of Drosophila, Proc. Natl. Acad. Sci. USA, 88, 263, 10.1073/pnas.88.1.263

Senthilkumar, 2009, Novel motifs distinguish multiple homologues of Polycomb in vertebrates: expansion and diversification of the epigenetic toolkit, BMC Genomics, 10, 549, 10.1186/1471-2164-10-549

Aravind, 1998, AT-hook motifs identified in a wide variety of DNA-binding proteins, Nucleic Acids Res., 26, 4413, 10.1093/nar/26.19.4413

Colas, 2008, Effective chromosome pairing requires chromatin remodeling at the onset of meiosis, Proc. Natl. Acad. Sci. USA, 105, 6075, 10.1073/pnas.0801521105

Webster, 2005, Meiotic and epigenetic defects in Dnmt3L-knockout mouse spermatogenesis, Proc. Natl. Acad. Sci. USA, 102, 4068, 10.1073/pnas.0500702102

Bestor, 2004, Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L, Nature, 431, 96, 10.1038/nature02886

Dantzer, 2006, Poly(ADP-ribose) polymerase-2 contributes to the fidelity of male meiosis I and spermiogenesis, Proc. Natl. Acad. Sci. USA., 103, 14854, 10.1073/pnas.0604252103

Baumann, 2006, Lsh is required for meiotic chromosome synapsis and retrotransposon silencing in female germ cells, Nat. Cell. Biol., 8, 1448, 10.1038/ncb1513

Miyagishima, 2003, Dissociation of mammalian Polycomb-group proteins, Ring1B and Rae28/Ph1, from the chromatin correlates with configuration changes of the chromatin in mitotic and meiotic prophase, Histochem. Cell Biol., 120, 111, 10.1007/s00418-003-0551-2

Balicky, 2004, A proposed role for the Polycomb group protein dRING in meiotic sister-chromatid cohesion, Chromosoma, 112, 231, 10.1007/s00412-003-0266-0

Sharma, 2010, MOF and Histone H4 Acetylation at Lysine 16 Are Critical for DNA Damage Response and Double-Strand Break Repair, Mol. Cell. Biol., 30, 3582, 10.1128/MCB.01476-09

Wu, 2009, Loss of YY1 Impacts the Heterochromatic State and Meiotic Double-Strand Breaks during Mouse Spermatogenesis, Mol. Cell. Biol., 29, 6245, 10.1128/MCB.00679-09

Nakayama, 2000, A chromodomain protein, Swi6, performs imprinting functions in fission yeast during mitosis and meiosis, Cell, 101, 307, 10.1016/S0092-8674(00)80840-5

Libby, 2002, The mouse meiotic mutation mei1 disrupts chromosome synapsis with sexually dimorphic consequences for meiotic progression, Dev. Biol., 242, 174, 10.1006/dbio.2001.0535

Yuan, 2002, Female germ cell aneuploidy and embryo death in mice lacking the meiosis-specific protein SCP3, Science, 296, 115, 10.1126/science.1070594

Viveiros, 2004, ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes, Dev. Biol., 272, 1, 10.1016/j.ydbio.2003.12.012

Ostrer, 2007, A cellular study of human testis development, Sex. Dev., 1, 286, 10.1159/000108930