全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
PLOS Genetics  2015 

Ancestral Chromatin Configuration Constrains Chromatin Evolution on Differentiating Sex Chromosomes in Drosophila

DOI: 10.1371/journal.pgen.1005331

Full-Text   Cite this paper   Add to My Lib

Abstract:

Sex chromosomes evolve distinctive types of chromatin from a pair of ancestral autosomes that are usually euchromatic. In Drosophila, the dosage-compensated X becomes enriched for hyperactive chromatin in males (mediated by H4K16ac), while the Y chromosome acquires silencing heterochromatin (enriched for H3K9me2/3). Drosophila autosomes are typically mostly euchromatic but the small dot chromosome has evolved a heterochromatin-like milieu (enriched for H3K9me2/3) that permits the normal expression of dot-linked genes, but which is different from typical pericentric heterochromatin. In Drosophila busckii, the dot chromosomes have fused to the ancestral sex chromosomes, creating a pair of ‘neo-sex’ chromosomes. Here we collect genomic, transcriptomic and epigenomic data from D. busckii, to investigate the evolutionary trajectory of sex chromosomes from a largely heterochromatic ancestor. We show that the neo-sex chromosomes formed <1 million years ago, but nearly 60% of neo-Y linked genes have already become non-functional. Expression levels are generally lower for the neo-Y alleles relative to their neo-X homologs, and the silencing heterochromatin mark H3K9me2, but not H3K9me3, is significantly enriched on silenced neo-Y genes. Despite rampant neo-Y degeneration, we find that the neo-X is deficient for the canonical histone modification mark of dosage compensation (H4K16ac), relative to autosomes or the compensated ancestral X chromosome, possibly reflecting constraints imposed on evolving hyperactive chromatin in an originally heterochromatic environment. Yet, neo-X genes are transcriptionally more active in males, relative to females, suggesting the evolution of incipient dosage compensation on the neo-X. Our data show that Y degeneration proceeds quickly after sex chromosomes become established through genomic and epigenetic changes, and are consistent with the idea that the evolution of sex-linked chromatin is influenced by its ancestral configuration.

References

[1]  Bull JJ. Evolution of sex determining mechanisms: The Benjamin/Cummings Publishing Company, Inc.; 1983.
[2]  Bachtrog D. Y-chromosome evolution: emerging insights into processes of Y-chromosome degeneration. Nat Rev Genet. 2013;14(2):113–24. doi: 10.1038/Nrg3366 pmid:WOS:000314622000011.
[3]  Zhou Q, Ellison CE, Kaiser VB, Alekseyenko AA, Gorchakov AA, Bachtrog D. The epigenome of evolving Drosophila neo-sex chromosomes: dosage compensation and heterochromatin formation. PLoS biology. 2013;11(11):e1001711. Epub 2013/11/23. doi: 10.1371/journal.pbio.1001711 pmid:24265597; PubMed Central PMCID: PMC3825665.
[4]  Conrad T, Akhtar A. Dosage compensation in Drosophila melanogaster: epigenetic fine-tuning of chromosome-wide transcription. Nat Rev Genet. 2011;13(2):123–34. doi: 10.1038/nrg3124 pmid:22251873.
[5]  Disteche CM. Dosage compensation of the sex chromosomes. Annual review of genetics. 2012;46:537–60. doi: 10.1146/annurev-genet-110711-155454 pmid:22974302; PubMed Central PMCID: PMC3767307.
[6]  Marais GA, Nicolas M, Bergero R, Chambrier P, Kejnovsky E, Moneger F, et al. Evidence for degeneration of the Y chromosome in the dioecious plant Silene latifolia. Current biology: CB. 2008;18(7):545–9. doi: 10.1016/j.cub.2008.03.023 pmid:18394889.
[7]  Zhang W, Wang X, Yu Q, Ming R, Jiang J. DNA methylation and heterochromatinization in the male-specific region of the primitive Y chromosome of papaya. Genome research. 2008;18(12):1938–43. doi: 10.1101/gr.078808.108 pmid:18593814; PubMed Central PMCID: PMC2593574.
[8]  Yoshida K, Makino T, Yamaguchi K, Shigenobu S, Hasebe M, Kawata M, et al. Sex chromosome turnover contributes to genomic divergence between incipient stickleback species. Plos Genet. 2014;10(3):e1004223. doi: 10.1371/journal.pgen.1004223. pmid:24625862
[9]  Zhou Q, Bachtrog D. Chromosome-wide gene silencing initiates Y degeneration in Drosophila. Current biology: CB. 2012;22(6):522–5. doi: 10.1016/j.cub.2012.01.057 pmid:22365853.
[10]  Charlesworth B, Charlesworth D. The degeneration of Y chromosomes. Philos Trans R Soc Lond B Biol Sci. 2000;355(1403):1563–72. Epub 2000/12/29. pmid:11127901; PubMed Central PMCID: PMC1692900. doi: 10.1098/rstb.2000.0717
[11]  Zhou Q, Bachtrog D. Sex-specific adaptation drives early sex chromosome evolution in Drosophila. Science. 2012;337(6092):341–5. Epub 2012/07/24. doi: 10.1126/science.1225385 pmid:22822149.
[12]  Steinemann M, Steinemann S. Enigma of Y chromosome degeneration: neo-Y and neo-X chromosomes of Drosophila miranda a model for sex chromosome evolution. Genetica. 1998;102-103(1–6):409–20. Epub 1998/08/28. pmid:9720292. doi: 10.1007/978-94-011-5210-5_33
[13]  Bachtrog D, Hom E, Wong KM, Maside X, de Jong P. Genomic degradation of a young Y chromosome in Drosophila miranda. Genome Biol. 2008;9(2):R30. Epub 2008/02/14. doi: gb-2008-9-2-r30 [pii] doi: 10.1186/gb-2008-9-2-r30 pmid:18269752.
[14]  Alekseyenko AA, Ellison CE, Gorchakov AA, Zhou Q, Kaiser VB, Toda N, et al. Conservation and de novo acquisition of dosage compensation on newly evolved sex chromosomes in Drosophila. Genes & development. 2013;27(8):853–8. Epub 2013/05/01. doi: 10.1101/gad.215426.113 pmid:23630075; PubMed Central PMCID: PMC3650223.
[15]  Ellison CE, Bachtrog D. Dosage compensation via transposable element mediated rewiring of a regulatory network. Science. 2013;342(6160):846–50. Epub 2013/11/16. doi: 10.1126/science.1239552 pmid:24233721.
[16]  Marin I, Franke A, Bashaw GJ, Baker BS. The dosage compensation system of Drosophila is co-opted by newly evolved X chromosomes. Nature. 1996;383(6596):160–3. doi: 10.1038/383160a0 pmid:WOS:A1996VG14800049.
[17]  Krivshenko J. New Evidence for the Homology of the Short Euchromatic Elements of the X and Y Chromosomes of Drosophila Busckii with the Microchromosome of Drosophila Melanogaster. Genetics. 1959;44(6):1027–40. Epub 1959/11/01. pmid:17247874; PubMed Central PMCID: PMC1224414.
[18]  Krivshenko JD. A cytogenetic study of the X chromosome of Drosophila busckii and its relation to phylogeny. Proceedings of the National Academy of Sciences of the United States of America. 1955;41(12):1071–9. Epub 1955/12/15. pmid:16589798; PubMed Central PMCID: PMC528199. doi: 10.1073/pnas.41.12.1071
[19]  Vicoso B, Bachtrog D. Reversal of an ancient sex chromosome to an autosome in Drosophila. Nature. 2013;499(7458):332–5. Epub 2013/06/25. doi: 10.1038/nature12235 pmid:23792562.
[20]  Vicoso B, Bachtrog D. Numerous transitions of sex chromosomes in Diptera. PLoS biology. 2015;in press.
[21]  Hochman B. The fourth chromosome of Drosophila melanogaster. Genetic Biology of the Drosophila (USA). 1976.
[22]  Jensen MA, Charlesworth B, Kreitman M. Patterns of genetic variation at a chromosome 4 locus of Drosophila melanogaster and D-simulans. Genetics. 2002;160(2):493–507. pmid:WOS:000174097600015.
[23]  Arguello JR, Zhang Y, Kado T, Fan C, Zhao R, Innan H, et al. Recombination yet inefficient selection along the Drosophila melanogaster subgroup's fourth chromosome. Molecular biology and evolution. 2010;27(4):848–61. doi: 10.1093/molbev/msp291 pmid:20008457; PubMed Central PMCID: PMC2877538.
[24]  Adams MD, Celniker SE, Holt RA, Evans CA, Gocayne JD, Amanatides PG, et al. The genome sequence of Drosophila melanogaster. Science. 2000;287(5461):2185–95. Epub 2000/03/25. pmid:10731132. doi: 10.1126/science.287.5461.2185
[25]  Haddrill PR, Halligan DL, Tomaras D, Charlesworth B. Reduced efficacy of selection in regions of the Drosophila genome that lack crossing over. Genome biology. 2007;8(2):R18. pmid:17284312 doi: 10.1186/gb-2007-8-2-r18
[26]  Campos JL, Charlesworth B, Haddrill PR. Molecular evolution in nonrecombining regions of the Drosophila melanogaster genome. Genome biology and evolution. 2012;4(3):278–88. doi: 10.1093/gbe/evs010 pmid:22275518; PubMed Central PMCID: PMC3318434.
[27]  Riddle NC, Minoda A, Kharchenko PV, Alekseyenko AA, Schwartz YB, Tolstorukov MY, et al. Plasticity in patterns of histone modifications and chromosomal proteins in Drosophila heterochromatin. Genome research. 2011;21(2):147–63. Epub 2010/12/24. doi: 10.1101/gr.110098.110 pmid:21177972; PubMed Central PMCID: PMC3032919.
[28]  Larsson J, Chen JD, Rasheva V, Rasmuson-Lestander A, Pirrotta V. Painting of fourth, a chromosome-specific protein in Drosophila. Proceedings of the National Academy of Sciences of the United States of America. 2001;98(11):6273–8. Epub 2001/05/17. doi: 10.1073/pnas.111581298 pmid:11353870; PubMed Central PMCID: PMC33458.
[29]  Larsson J, Svensson MJ, Stenberg P, Makitalo M. Painting of fourth in genus Drosophila suggests autosome-specific gene regulation. Proceedings of the National Academy of Sciences of the United States of America. 2004;101(26):9728–33. Epub 2004/06/24. doi: 10.1073/pnas.0400978101 pmid:15210994; PubMed Central PMCID: PMC470743.
[30]  Grimaldi DA. A phylogenetic, revised classification of genera in the Drosophilidae (Diptera). B Am Mus Nat Hist. 1990;(197):1–139. pmid:WOS:A1990EF89200001.
[31]  Larsson J, Meller VH. Dosage compensation, the origin and the afterlife of sex chromosomes. Chromosome research: an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology. 2006;14(4):417–31. Epub 2006/07/06. doi: 10.1007/s10577-006-1064-3 pmid:16821137.
[32]  Bhutkar A, Schaeffer SW, Russo SM, Xu M, Smith TE, Gelbart WM. Chromosomal rearrangement inferred from comparisons of 12 Drosophila genomes. Genetics. 2008;179(3):1657–80. doi: 10.1534/Genetics.107.086108 pmid:WOS:000258313400039.
[33]  Graveley BR, Brooks AN, Carlson JW, Duff MO, Landolin JM, Yang L, et al. The developmental transcriptome of Drosophila melanogaster. Nature. 2011;471(7339):473–9. Epub 2010/12/24. doi: 10.1038/nature09715 pmid:21179090; PubMed Central PMCID: PMC3075879.
[34]  Sturgill D, Zhang Y, Parisi M, Oliver B. Demasculinization of X chromosomes in the Drosophila genus. Nature. 2007;450(7167):238–41. doi: 10.1038/nature06330 pmid:17994090; PubMed Central PMCID: PMC2386140.
[35]  van der Linde K, Houle D, Spicer GS, Steppan SJ. A supermatrix-based molecular phylogeny of the family Drosophilidae. Genet Res. 2010;92(1):25–38. Epub 2010/05/04. doi: 10.1017/S001667231000008X pmid:20433773.
[36]  Vicoso B, Bachtrog D. Numerous transitions of sex chromosomes in Diptera. PLoS biology. 2015;13(4):e1002078. doi: 10.1371/journal.pbio.1002078. pmid:25879221
[37]  Kwiatowski J, Ayala FJ. Phylogeny of Drosophila and related genera: conflict between molecular and anatomical analyses. Mol Phylogenet Evol. 1999;13(2):319–28. doi: 10.1006/mpev.1999.0657 pmid:10603260.
[38]  Schrider DR, Houle D, Lynch M, Hahn MW. Rates and genomic consequences of spontaneous mutational events in Drosophila melanogaster. Genetics. 2013;194(4):937–54. doi: 10.1534/genetics.113.151670 pmid:23733788; PubMed Central PMCID: PMC3730921.
[39]  Bachtrog D. The temporal dynamics of processes underlying Y chromosome degeneration. Genetics. 2008;179(3):1513–25. doi: 10.1534/genetics.107.084012 pmid:18562655; PubMed Central PMCID: PMC2475751.
[40]  Kaiser VB, Charlesworth B. The effects of deleterious mutations on evolution in non-recombining genomes. Trends Genet. 2009;25(1):9–12. doi: 10.1016/j.tig.2008.10.009 pmid:19027982.
[41]  Haddrill PR, Halligan DL, Tomaras D, Charlesworth B. Reduced efficacy of selection in regions of the Drosophila genome that lack crossing over. Genome biology. 2007;8(2). doi: Artn R18 doi: 10.1186/Gb-2007-8-2-R18 pmid:WOS:000246076300006.
[42]  Lindsley DL, Sandler L, Baker BS, Carpenter AT, Denell RE, Hall JC, et al. Segmental aneuploidy and the genetic gross structure of the Drosophila genome. Genetics. 1972;71(1):157–84. Epub 1972/05/01. pmid:4624779; PubMed Central PMCID: PMC1212769.
[43]  Powell JR, Dion K, Papaceit M, Aguade M, Vicario S, Garrick RC. Nonrecombining genes in a recombination environment: the Drosophila "dot" chromosome. Molecular biology and evolution. 2011;28(1):825–33. doi: 10.1093/molbev/msq258 pmid:20940345; PubMed Central PMCID: PMC3002241.
[44]  Kaiser VB, Zhou Q, Bachtrog D. Nonrandom gene loss from the Drosophila miranda neo-Y chromosome. Genome biology and evolution. 2011;3:1329–37. Epub 2011/10/12. doi: 10.1093/gbe/evr103 pmid:21987387; PubMed Central PMCID: PMC3236567.
[45]  Riddle NC, Jung YL, Gu TT, Alekseyenko AA, Asker D, Gui HX, et al. Enrichment of HP1a on Drosophila Chromosome 4 Genes Creates an Alternate Chromatin Structure Critical for Regulation in this Heterochromatic Domain. Plos Genet. 2012;8(9). doi: Artn E1002954 doi: 10.1371/Journal.Pgen.1002954 pmid:WOS:000309817900029.
[46]  Gelbart ME, Larschan E, Peng S, Park PJ, Kuroda MI. Drosophila MSL complex globally acetylates H4K16 on the male X chromosome for dosage compensation. Nature structural & molecular biology. 2009;16(8):825–32. Epub 2009/08/04. doi: 10.1038/nsmb.1644 pmid:19648925; PubMed Central PMCID: PMC2722042.
[47]  Stenberg P, Larsson J. Buffering and the evolution of chromosome-wide gene regulation. Chromosoma. 2011;120(3):213–25. Epub 2011/04/21. doi: 10.1007/s00412-011-0319-8 pmid:21505791; PubMed Central PMCID: PMC3098985.
[48]  Kind J, Vaquerizas JM, Gebhardt P, Gentzel M, Luscombe NM, Bertone P, et al. Genome-wide analysis reveals MOF as a key regulator of dosage compensation and gene expression in Drosophila. Cell. 2008;133(5):813–28. doi: 10.1016/j.cell.2008.04.036. pmid:18510926
[49]  Johansson AM, Stenberg P, Allgardsson A, Larsson J. POF regulates the expression of genes on the fourth chromosome in Drosophila melanogaster by binding to nascent RNA. Mol Cell Biol. 2012;32(11):2121–34. doi: 10.1128/MCB.06622-11 pmid:22473994; PubMed Central PMCID: PMC3372238.
[50]  Spierer A, Begeot F, Spierer P, Delattre M. SU(VAR)3-7 links heterochromatin and dosage compensation in Drosophila. Plos Genet. 2008;4(5):e1000066. Epub 2008/05/03. doi: 10.1371/journal.pgen.1000066 pmid:18451980; PubMed Central PMCID: PMC2320979.
[51]  Gnerre S, Maccallum I, Przybylski D, Ribeiro FJ, Burton JN, Walker BJ, et al. High-quality draft assemblies of mammalian genomes from massively parallel sequence data. Proceedings of the National Academy of Sciences of the United States of America. 2011;108(4):1513–8. Epub 2010/12/29. doi: 10.1073/pnas.1017351108 pmid:21187386; PubMed Central PMCID: PMC3029755.
[52]  Trapnell C, Pachter L, Salzberg SL. TopHat: discovering splice junctions with RNA-Seq. Bioinformatics. 2009;25(9):1105–11. Epub 2009/03/18. doi: 10.1093/bioinformatics/btp120 pmid:19289445; PubMed Central PMCID: PMC2672628.
[53]  Trapnell C, Williams BA, Pertea G, Mortazavi A, Kwan G, van Baren MJ, et al. Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. Nature biotechnology. 2010;28(5):511–5. Epub 2010/05/04. doi: 10.1038/nbt.1621 pmid:20436464; PubMed Central PMCID: PMC3146043.
[54]  Cantarel BL, Korf I, Robb SM, Parra G, Ross E, Moore B, et al. MAKER: an easy-to-use annotation pipeline designed for emerging model organism genomes. Genome research. 2008;18(1):188–96. Epub 2007/11/21. doi: 10.1101/gr.6743907 pmid:18025269; PubMed Central PMCID: PMC2134774.
[55]  Leung W, Shaffer CD, Cordonnier T, Wong J, Itano MS, Slawson Tempel EE, et al. Evolution of a distinct genomic domain in Drosophila: comparative analysis of the dot chromosome in Drosophila melanogaster and Drosophila virilis. Genetics. 2010;185(4):1519–34. doi: 10.1534/genetics.110.116129 pmid:20479145; PubMed Central PMCID: PMC2927774.
[56]  DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet. 2011;43(5):491-+. doi: 10.1038/Ng.806 pmid:WOS:000289972600023.
[57]  Langmead B, Salzberg SL. Fast gapped-read alignment with Bowtie 2. Nature methods. 2012;9(4):357–9. Epub 2012/03/06. doi: 10.1038/nmeth.1923 pmid:22388286; PubMed Central PMCID: PMC3322381.
[58]  Birney E, Clamp M, Durbin R. GeneWise and genomewise. Genome Res. 2004;14(5):988–95. doi: 10.1101/Gr.1865504 pmid:WOS:000221171700026.
[59]  Abascal F, Zardoya R, Telford MJ. TranslatorX: multiple alignment of nucleotide sequences guided by amino acid translations. Nucleic acids research. 2010;38(Web Server issue):W7–13. Epub 2010/05/04. doi: 10.1093/nar/gkq291 pmid:20435676; PubMed Central PMCID: PMC2896173.
[60]  Castresana J. Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. Molecular biology and evolution. 2000;17(4):540–52. Epub 2000/03/31. pmid:10742046. doi: 10.1093/oxfordjournals.molbev.a026334
[61]  Stamatakis A. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics. 2014. Epub 2014/01/24. doi: 10.1093/bioinformatics/btu033 pmid:24451623.
[62]  Yang Z. PAML 4: phylogenetic analysis by maximum likelihood. Molecular biology and evolution. 2007;24(8):1586–91. Epub 2007/05/08. doi: 10.1093/molbev/msm088 pmid:17483113.
[63]  Alekseyenko AA, Peng SY, Larschan E, Gorchakov AA, Lee OK, Kharchenko P, et al. A sequence motif within chromatin entry sites directs MSL establishment on the Drosophila X chromosome. Cell. 2008;134(4):599–609. doi: 10.1016/J.Cell.2008.06.033 pmid:WOS:000258665800014.
[64]  Zhang Y, Liu T, Meyer CA, Eeckhoute J, Johnson DS, Bernstein BE, et al. Model-based analysis of ChIP-Seq (MACS). Genome biology. 2008;9(9):R137. Epub 2008/09/19. doi: 10.1186/gb-2008-9-9-r137 pmid:18798982; PubMed Central PMCID: PMC2592715.
[65]  Machanick P, Bailey TL. MEME-ChIP: motif analysis of large DNA datasets. Bioinformatics. 2011;27(12):1696–7. Epub 2011/04/14. doi: 10.1093/bioinformatics/btr189 pmid:21486936; PubMed Central PMCID: PMC3106185.
[66]  Conrad T, Cavalli FM, Vaquerizas JM, Luscombe NM, Akhtar A. Drosophila dosage compensation involves enhanced Pol II recruitment to male X-linked promoters. Science. 2012;337(6095):742–6. doi: 10.1126/science.1221428 pmid:22821985.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133