Identification of the Drosophila X chromosome: The long and short of it

References

• Charlesworth B. The evolution of sex chromosomes. Science 1991; 251:1030-3; PMID:1998119; http://dx.doi.org/10.1126/science.1998119
   PubMed Web of Science ®Google Scholar
• Lucchesi J, Kelly W, Panning B. Chromatin remodeling in dosage compensation. Ann Rev Genet 2005; 39:615-51; http://dx.doi.org/10.1146/annurev.genet.39.073003.094210
   PubMed Web of Science ®Google Scholar
• Deng X, Hiatt JB, Nguyen DK, Ercan S, Sturgill D, Hillier LW, Schlesinger F, Davis CA, Reinke VJ, Gingeras TR, et al. Evidence for compensatory upregulation of exressed X-linked genes in mammals, Caenorhabditis elegans and Drosophila melanogaster. Nat Genet 2011; 43:1179-85; http://dx.doi.org/10.1038/ng.948
   PubMed Web of Science ®Google Scholar
• Hall LL, Lawrence JB. XIST RNA and architecture of the inactive X chromosome: implications for the repeat genome. Cold Spring Harb Symp Quant Biol 2010; 75:345-56; http://dx.doi.org/10.1101/sqb.2010.75.030
   PubMedGoogle Scholar
• Leung KN, Panning B. X-inactivation: Xist RNA uses chromosome contacts to coat the X. Curr Biol 2014; 24:R80-2; PMID:24456982; http://dx.doi.org/10.1016/j.cub.2013.11.052
   PubMedGoogle Scholar
• Kong Y, Meller VH. How to get extra performance from a chromosome: recognition and modification of the X chromosome in male Drosophila melanogaster. Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics: John Wiley & Sons, Ltd, 2007; 15
   Google Scholar
• Kelley R, Solovyeva I, Lyman L, Richman R, Solovyev V, Kuroda M. Expression of MSL2 causes assembly of dosage compensation regulators on the X chromosomes and female lethality in Drosophila. Cell 1995; 81:867-77; PMID:7781064; http://dx.doi.org/10.1016/0092-8674(95)90007-1
   PubMed Web of Science ®Google Scholar
• Alekseyenko AA, Larschan E, Lai WR, Park PJ, Kuroda MI. High-resolution ChIP-chip analysis reveals that the Drosophila MSL complex selectively identifies active genes on the male X chromosome. Genes Dev 2006; 20:848-57; PMID:16547173; http://dx.doi.org/10.1101/gad.1400206
   PubMed Web of Science ®Google Scholar
• Akhtar A, Becker P. Activation of transcription through histone H4 acetylation by MOF, and acetyltransferase essential for dosage compensation in Drosophila. Mol Cell 2000; 5:367-75; PMID:10882077; http://dx.doi.org/10.1016/S1097-2765(00)80431-1
   PubMed Web of Science ®Google Scholar
• Smith ER, Pannuti A, Gu W, Steurnagel A, Cook RJ, Allis CD, Lucchesi JC. The Drosophila MSL complex acetylates histone H4 at lysine 16, a chromatin modification linked to dosage compensation. Mol Cell Biol 2000; 20:312-18; http://dx.doi.org/10.1128/MCB.20.1.312-318.2000
   PubMed Web of Science ®Google Scholar
• Shogren-Knaak M, Ishii H, Sun J-M, Pazin MJ, Davie JR, Peterson CL. Histone H4-K16 acetylation controls chromatin structure and protein interactions. Science 2006; 311:844-47; PMID:16469925; http://dx.doi.org/10.1126/science.1124000
   PubMed Web of Science ®Google Scholar
• Liu Y, Lu C, Yang Y, Fan Y, Yang R, Liu CF, Korolev N, Nordenskiold L. Influence of histone tails and H4 tail acetylations on nucleosome-nucleosome interactions. J Mol Biol 2011; 414:749-64; http://dx.doi.org/10.1016/j.jmb.2011.10.031
   PubMed Web of Science ®Google Scholar
• Larschan E, Bishop EP, Kharchenko PV, Core LJ, Lis JT, Park PJ, Kuroda MI. X chromosome dosage compensation via enhanced transcriptional elongation in Drosophila. Nature 2011; 471:115-8; PMID:21368835; http://dx.doi.org/10.1038/nature09757
   PubMed Web of Science ®Google Scholar
• Ferrari F, Plachetka A, Alekseyenko AA, Jung YL, Ozsolak F, Kharchenko PV, Park PJ, Kuroda MI. Jump start and gain model for dosage compensation in Drosophila based on direct sequencing of nascent transcripts. Cell Rep 2013; 5:629-36; PMID:24183666; http://dx.doi.org/10.1016/j.celrep.2013.09.037
   PubMed Web of Science ®Google Scholar
• Conrad T, Cavalli FMG, Vaquerizas JM, Luscombe NM, Akhtar A. Drosophila dosage compensation involves enhanced Pol II recruitment to male X-linked promoters. Science 2012; 337:742-46; PMID:22821985; http://dx.doi.org/10.1126/science.1221428
   PubMed Web of Science ®Google Scholar
• Wu L, Li L, Zhou B, Qin Z, Dou Y. H2B ubiquitylation promotes RNA Pol II processivity via PAF1 and pTEFb. Mol Cell 2014; 54:920-31; PMID:24837678; http://dx.doi.org/10.1016/j.molcel.2014.04.013
   PubMed Web of Science ®Google Scholar
• Wu L, Zee BM, Wang Y, Garcia BA, Dou Y. The RING finger protein MSL2 in the MOF complex is an E3 ubiquitin ligase for H2B K34 and is involved in crosstalk with H3 K4 and K79 methylation. Mol Cell 2011; 43:132-44; PMID:21726816; http://dx.doi.org/10.1016/j.molcel.2011.05.015
   PubMed Web of Science ®Google Scholar
• Lyman LM, Copps K, Rastelli L, Kelley RL, Kuroda MI. Drosophila Male-Specific Lethal 2 protein: structure/function analysis and dependence on MSL1 for chromosome association. Genetics 1997; 147:1743-53; PMID:9409833
   PubMed Web of Science ®Google Scholar
• Alekseyenko AA, Peng S, Larschan E, Gorchakov AA, Lee OK, Kharchenko P, McGrath SD, Wang CI, Mardis ER, Park PJ, et al. A sequence motif within chromatin entry sites directs MSL establishment on the Drosophila X chromosome. Cell 2008; 134:599-609; PMID:18724933; http://dx.doi.org/10.1016/j.cell.2008.06.033
   PubMed Web of Science ®Google Scholar
• Straub T, Grimaud C, Gilfillan GD, Mitterweger A, Becker PB. The chromosomal high-affinity binding sites for the Drosophila dosage compensation complex. PLoS Genet 2008; 4:e1000302; PMID:19079572; http://dx.doi.org/10.1371/journal.pgen.1000302
   PubMed Web of Science ®Google Scholar
• Soruco MM, Chery J, Bishop EP, Siggers T, Tolstorukov MY, Leydon AR, Sugden AU, Goebel K, Feng J, Xia P, et al. The CLAMP protein links the MSL complex to the X chromosome during Drosophila dosage compensation. Genes Dev 2013; 27:1551-6; PMID:23873939; http://dx.doi.org/10.1101/gad.214585.113
   PubMed Web of Science ®Google Scholar
• Kind J, Akhtar A. Cotranscriptional recruitment of the dosage compensation complex to X-linked target genes. Genes Dev 2007; 21:2030-40; PMID:17699750; http://dx.doi.org/10.1101/gad.430807
   PubMed Web of Science ®Google Scholar
• Larschan E, Alekseyenko AA, Gortchakov AA, Peng S, Li B, Yang P, Workman JL, Park PJ, Kuroda MI. MSL complex is attracted to genes marked by H3K36 trimethylation using a sequence-independent mechanism. Mol Cell 2007; 28:121-33; PMID:17936709; http://dx.doi.org/10.1016/j.molcel.2007.08.011
   PubMed Web of Science ®Google Scholar
• Sural TH, Peng S, Li B, Workman JL, Park PJ, Kuroda MI. The MSL3 chromodomain directs a key targeting step for dosage compensation of the Drosophila melanogaster X chromosome. Nat Struct Mol Biol 2008; 15:1318-25; PMID:19029895; http://dx.doi.org/10.1038/nsmb.1520
   PubMed Web of Science ®Google Scholar
• Bell O, Conrad T, Kind J, Wirbelauer C, Akhtar A, Schubeler D. Transcription-coupled methylation of histone H3 at lysine 36 regulates dosage compensation by enhancing recruitment of the MSL complex in Drosophila melanogaster. Mol Cell Biol 2008; 28:3401-9; PMID:18347056; http://dx.doi.org/10.1128/MCB.00006-08
   PubMed Web of Science ®Google Scholar
• Gelbart ME, Kuroda MI. Drosophila dosage compensation: a complex voyage to the X chromosome. Development 2009; 136:1399-410; PMID:19363150; http://dx.doi.org/10.1242/dev.029645
   PubMed Web of Science ®Google Scholar
• Menon DU, Meller VH. A role for siRNA in X-chromosome dosage compensation in Drosophila melanogaster. Genetics 2012; 191:1023-8; PMID:22554892; http://dx.doi.org/10.1534/genetics.112.140236
   PubMed Web of Science ®Google Scholar
• Meller VH, Wu KH, Roman G, Kuroda M, David R. roX1 RNA paints the X chromosome of male Drosophila and is regulated by the dosage compensation system. Cell 1997; 88:445-57; PMID:9038336; http://dx.doi.org/10.1016/S0092-8674(00)81885-1
   PubMed Web of Science ®Google Scholar
• Meller VH, Rattner B. The roX genes encode redundant male specific lethal transcripts required for targeting of the MSL complex. EMBO J 2002; 21:1084-91; PMID:11867536; http://dx.doi.org/10.1093/emboj/21.5.1084
   PubMed Web of Science ®Google Scholar
• Deng X, Meller VH. roX RNAs are required for increased expression of X-linked genes in Drosophila melanogaster males. Genetics 2006; 174:1859-66; PMID:17028315; http://dx.doi.org/10.1534/genetics.106.064568
   PubMed Web of Science ®Google Scholar
• Oh H, Park Y, Kuroda MI. Local spreading of MSL complexes from roX genes on the Drosophila X chromosome. Genes Dev 2003; 17:1334-9; PMID:12782651; http://dx.doi.org/10.1101/gad.1082003
   PubMed Web of Science ®Google Scholar
• Kageyama Y, Mengus G, Gilfillan G, Kennedy HG, Stuckenholz C, Kelley RL, Becker PB, Kuroda MI. Association and spreading of the Drosophila dosage compensation complex from a discrete roX1 chromatin entry site. EMBO J 2001; 20:2236-45; PMID:11331589; http://dx.doi.org/10.1093/emboj/20.9.2236
   PubMed Web of Science ®Google Scholar
• Kelley R, Meller VH, Gordadze P, Roman G, Davis R, Kuroda M. Epigenetic spreading of the Drosophila dosage compensation complex from roX RNA genes into flanking chromatin. Cell 1999; 98:513-22; PMID:10481915; http://dx.doi.org/10.1016/S0092-8674(00)81979-0
   PubMed Web of Science ®Google Scholar
• Fagegaltier D, Bouge AL, Berry B, Poisot E, Sismeiro O, Coppee JY, Theodore L, Voinnet O, Antoniewski C. The endogenous siRNA pathway is involved in heterochromatin formation in Drosophila. Proc Natl Acad Sci USA 2009; 106:21258-63; PMID:19948966; http://dx.doi.org/10.1073/pnas.0809208105
   PubMed Web of Science ®Google Scholar
• Brower-Toland B, Findley SD, Jiang L, Liu L, Yin H, Dus M, Zhou P, Elgin SCR, Lin H. Drosophila PIWI associates with chromatin and interacts directly with HP1a. Genes Dev 2007; 21:2300-11; PMID:17875665; http://dx.doi.org/10.1101/gad.1564307
   PubMed Web of Science ®Google Scholar
• Gu T, Elgin SC. Maternal depletion of Piwi, a component of the RNAi system, impacts heterochromatin formation in Drosophila. PLoS Genet 2013; 9:e1003780; PMID:24068954; http://dx.doi.org/10.1371/journal.pgen.1003780
   PubMedGoogle Scholar
• Pal-Bhadra M, Leibovitch Ba, Gandhi SG, Rao M, Bhadra U, Birchler Ja, Elgin SCR. Heterochromatic silencing and HP1 localization in Drosophila are dependent on the RNAi machinery. Science 2004; 303:669-72; PMID:14752161; http://dx.doi.org/10.1126/science.1092653
   PubMed Web of Science ®Google Scholar
• Cernilogar FM, Onorati MC, Kothe GO, Burroughs AM, Parsi KM, Breiling A, Lo Sardo F, Saxena A, Miyoshi K, Siomi H, et al. Chromatin-associated RNA interference components contribute to transcriptional regulation in Drosophila. Nature 2011; 480:391-5; PMID:22056986; http://dx.doi.org/10.1038/nature10492
   PubMed Web of Science ®Google Scholar
• Buhler M, Verdel A, Moazed D. Tethering RITS to a nascent transcript initiates RNAi- and heterochromatin-dependent gene silencing. Cell 2006; 125:873-86; PMID:16751098; http://dx.doi.org/10.1016/j.cell.2006.04.025
   PubMed Web of Science ®Google Scholar
• Cam HP, Sugiyama T, Chen ES, Chen X, FitzGerald PC, Grewal SI. Comprehensive analysis of heterochromatin- and RNAi-mediated epigenetic control of the fission yeast genome. Nat Genet 2005; 37:809-19; PMID:15976807; http://dx.doi.org/10.1038/ng1602
   PubMed Web of Science ®Google Scholar
• Wang CI, Alekseyenko AA, LeRoy G, Elia AE, Gorchakov AA, Britton LM, Elledge SJ, Kharchenko PV, Garcia BA, Kuroda MI. Chromatin proteins captured by ChIP-mass spectrometry are linked to dosage compensation in Drosophila. Nat Structural Mol Biol 2013; 20:202-9; http://dx.doi.org/10.1038/nsmb.2477
   PubMed Web of Science ®Google Scholar
• Verdel A, Vavasseur A, Le Gorrec M, Touat-Todeschini L. Common themes in siRNA-mediated epigenetic silencing pathways. Int J Dev Biol 2009; 53:245-57; http://dx.doi.org/10.1387/ijdb.082691av
   PubMed Web of Science ®Google Scholar
• Kuhn GCS, Küttler H, Moreira-Filho O, Heslop-Harrison JS. The 1.688 repetitive DNA of drosophila: Concerted evolution at different genomic scales and association with genes. Mol Biol Evolution 2012; 29:7-11; http://dx.doi.org/10.1093/molbev/msr173
   PubMed Web of Science ®Google Scholar
• DiBartolomeis SM, Tartof KD, Jackson FR. A superfamily of Drosophila satellite related (SR) DNA repeats restricted to the X chromosome euchromatin. Nucleic Acids Res 1992; 20:1113-6; PMID:1549474; http://dx.doi.org/10.1093/nar/20.5.1113
   PubMed Web of Science ®Google Scholar
• Menon DU, Coarfa C, Xiao W, Gunaratne PH, Meller VH. siRNAs from an X-linked satellite repeat promote X-chromosome recognition in Drosophila melanogaster. Proc Natl Acad Sci USA 2014; 111:16460-5; PMID:25368194; http://dx.doi.org/10.1073/pnas.1410534111
   PubMed Web of Science ®Google Scholar
• Usakin L, Abad J, Vagin VV, de Pablos B, Villasante A, Gvozdev VA. Transcription of the 1.688 satellite DNA family is under the control of RNA interference machinery in Drosophila melanogaster ovaries. Genetics 2007; 176:1343-49; PMID:17409066; http://dx.doi.org/10.1534/genetics.107.071720
   PubMed Web of Science ®Google Scholar
• Kuhn G, Kuttler H, Moreira-Filho O, Heslop-Harrison J. The 1.688 repetitive DNA of Drosophila: concerted evolution at different genomic scales and association with genes. Mol Biol Evol 2011; 29(1):7-11
   PubMed Web of Science ®Google Scholar
• Gallach M. Recurrent turnover of chromosome-specific satellites in Drosophila. Genome Biol Evol 2014; 6:1279-86; http://dx.doi.org/10.1093/gbe/evu104
   PubMed Web of Science ®Google Scholar
• Meller VH. Initiation of dosage compensation in Drosophila embryos depends on expression of the roX RNAs. Mech Dev 2003; 120:759-67; http://dx.doi.org/10.1016/S0925-4773(03)00157-6
   PubMed Web of Science ®Google Scholar
• Wang CI, Alekseyenko Aa, LeRoy G, Elia AEH, Gorchakov Aa, Britton L-MP, Elledge SJ, Kharchenko PV, Garcia Ba, Kuroda MI. Chromatin proteins captured by ChIP-mass spectrometry are linked to dosage compensation in Drosophila. Nat Struct Mol Biol 2013; 20:202-9; http://dx.doi.org/10.1038/nsmb.2477
   PubMed Web of Science ®Google Scholar
• Su M, Han D, Boyd-Kirkup J, Yu X, Han JDJ. Evolution of Alu Elements toward Enhancers. Cell Rep 2014; 7:376-85; PMID:24703844; http://dx.doi.org/10.1016/j.celrep.2014.03.011
   PubMed Web of Science ®Google Scholar
• Johnson KD, Grass JA, Park C, Im H, Choi K, Bresnick EH. Highly restricted localization of RNA polymerase II within a locus control region of a tissue-specific chromatin domain. Mol Cell Biol 2003; 23:6484-93; PMID:12944475; http://dx.doi.org/10.1128/MCB.23.18.6484-6493.2003
   PubMed Web of Science ®Google Scholar
• Lam MTY, Li W, Rosenfeld MG, Glass CK. Enhancer RNAs and regulated transcriptional programs. Trends Biochem Sci 2014; 39:170-82; http://dx.doi.org/10.1016/j.tibs.2014.01.002
   PubMed Web of Science ®Google Scholar
• Mousavi K, Zare H, Dell'Orso S, Grontved L, Gutierrez-Cruz G, Derfoul A, Hager G, Sartorelli V. ERNAs Promote Transcription by Establishing Chromatin Accessibility at Defined Genomic Loci. Mol Cell 2013; 51:606-17; PMID:23993744; http://dx.doi.org/10.1016/j.molcel.2013.07.022
   PubMed Web of Science ®Google Scholar
• Cernilogar FM, Onorati MC, Kothe GO, Burroughs AM, Parsi KM, Breiling A, Sardo FL, Saxena A, Miyoshi K, Siomi H, et al. Chromatin-associated RNA interference components contribute to transcriptional regulation in Drosophila. Nature 2011; 480:391-5; PMID:22056986; http://dx.doi.org/10.1038/nature10492
   PubMed Web of Science ®Google Scholar
• Moshkovich N, Nisha P, Boyle PJ, Thompson BA, Dale RK, Lei EP. RNAi-independent role for Argonaute2 in CTCF/CP190 chromatin insulator function. Genes Dev 2011; 25:1686-701; PMID:21852534; http://dx.doi.org/10.1101/gad.16651211
   PubMed Web of Science ®Google Scholar
• Portnoy V, Huang V, Place RF, Li LC. Small RNA and transcriptional upregulation. Wiley Interdiscip Rev RNA 2011; 2:748-60; PMID:21823233; http://dx.doi.org/10.1002/wrna.90
   PubMed Web of Science ®Google Scholar
• Yin H, Lin H. An epigenetic activation role of Piwi and a Piwi-associated piRNA in Drosophila melanogaster. Nature 2007; 450:304-8; PMID:17952056; http://dx.doi.org/10.1038/nature06263
   PubMed Web of Science ®Google Scholar
• Nègre N, Brown CD, Ma L, Bristow CA, Miller SW, Wagner U, Kheradpour P, Eaton ML, Loriaux P, Sealfon R, et al. A cis-regulatory map of the Drosophila genome. Nature 2011; 471:527-31; http://dx.doi.org/10.1038/nature09990
   PubMed Web of Science ®Google Scholar
• Csink AK, Henikoff S. Something from nothing: the evolution and utility of satellite repeats. Trends Genet 1998; 14:200-4; http://dx.doi.org/10.1016/S0168-9525(98)01444-9
   PubMed Web of Science ®Google Scholar
• Ferree PM, Barbash DA. Species-specific heterochromatin prevents mitotic chromosome segregation to cause hybrid lethality in Drosophila. PLoS Biol 2009; 7:e1000234; PMID:19859525; http://dx.doi.org/10.1371/journal.pbio.1000234
   PubMed Web of Science ®Google Scholar
• Käs E, Laemmli UK. In vivo topoisomerase II cleavage of the Drosophila histone and satellite III repeats: DNA sequence and structural characteristics. EMBO J 1992; 11:705-16
   PubMed Web of Science ®Google Scholar
• Cugusi S, Ramos E, Ling H, Yokoyama R, Luk KM, Lucchesi JC. Topoisomerase II plays a role in dosage compensation inDrosophila. Transcription 2014; 4:238-50; http://dx.doi.org/10.4161/trns.26185
   Google Scholar
• Furuhashi H, Nakajima M, Hirose S. DNA supercoiling factor contributes to dosage compensation in Drosophila. Development 2006; 133:4475-83; PMID:17035293; http://dx.doi.org/10.1242/dev.02620
   PubMed Web of Science ®Google Scholar
• Mendjan S, Taipale M, Kind J, Holz H, Gebhardt P, Schelder M, Vermeulen M, Buscaino A, Duncan K, Mueller J, et al. Nuclear pore components are involved in the transcriptional regulation of dosage compensation in Drosophila. Mol Cell 2006; 21:811-23; PMID:16543150; http://dx.doi.org/10.1016/j.molcel.2006.02.007
   PubMed Web of Science ®Google Scholar
• Vaquerizas JM, Suyama R, Kind J, Miura K, Luscombe NM, Akhtar A. Nuclear pore proteins nup153 and megator define transcriptionally active regions in the Drosophila genome. PLoS Genet 2010; 6:e1000846; PMID:20174442; http://dx.doi.org/10.1371/journal.pgen.1000846
   PubMed Web of Science ®Google Scholar
• Grimaud C, Becker PB. The dosage compensation complex shapes the conformation of the X chromosome in Drosophila. Genes Dev 2009; 23:2490-5; PMID:19884256; http://dx.doi.org/10.1101/gad.539509
   PubMed Web of Science ®Google Scholar
• de Wit E, de Laat W. A decade of 3C technologies: insights into nuclear organization. Genes Dev 2012; 26:11-24; PMID:22215806; http://dx.doi.org/10.1101/gad.179804.111
   PubMed Web of Science ®Google Scholar
• Rao SS, Huntley MH, Durand NC, Stamenova EK, Bochkov ID, Robinson JT, Sanborn AL, Machol I, Omer AD, Lander ES, et al. A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping. Cell 2014; 159:1665-80; PMID:25497547; http://dx.doi.org/10.1016/j.cell.2014.11.021
   PubMed Web of Science ®Google Scholar
• Sexton T, Yaffe E, Kenigsberg E, Bantignies F, Leblanc B, Hoichman M, Parrinello H, Tanay A, Cavalli G. Three-dimensional folding and functional organization principles of the Drosophila genome. Cell 2012; 148:458-72; PMID:22265598; http://dx.doi.org/10.1016/j.cell.2012.01.010
   PubMed Web of Science ®Google Scholar
• O'Hare K, Chadwick B, Constantinou A, Davis A, Mitchelson A, Tudor M. A 5.9-kb tandem repeat at the euchromatin-heterochromatin boundary of the X chromosome of Drosophila melanogaster. Mol Genet Genomics 2002; 267:647-55; http://dx.doi.org/10.1007/s00438-002-0698-x
   PubMed Web of Science ®Google Scholar
• Horakova AH, Moseley SC, McLaughlin CR, Tremblay DC, Chadwick BP. The macrosatellite DXZ4 mediates CTCF-dependent long-range intrachromosomal interactions on the human inactive X chromosome. Human Mol Genet 2012; 21:4367-77; http://dx.doi.org/10.1093/hmg/dds270
   PubMed Web of Science ®Google Scholar
• Ottaviani A, Rival-Gervier S, Boussouar A, Foerster AM, Rondier D, Sacconi S, Desnuelle C, Gilson E, Magdinier F. The D4Z4 macrosatellite repeat acts as a CTCF and A-type lamins-dependent insulator in Facio-Scapulo-Humeral dystrophy. PLoS Genet 2009; 5:e1000394; PMID:19247430; http://dx.doi.org/10.1371/journal.pgen.1000394
   PubMed Web of Science ®Google Scholar
• Rival-Gervier S, Lo MY, Khattak S, Pasceri P, Lorincz MC, Ellis J. Kinetics and epigenetics of retroviral silencing in mouse embryonic stem cells defined by deletion of the D4Z4 element. Mol Ther 2013; 21:1536-50; http://dx.doi.org/10.1038/mt.2013.131
   PubMed Web of Science ®Google Scholar
• Lei EP, Corces VG. A long-distance relationship between RNAi and Polycomb. Cell 2006; 124:886-8; PMID:16530034; http://dx.doi.org/10.1016/j.cell.2006.02.026
   PubMed Web of Science ®Google Scholar
• Kuhn E, Viering M, Rhodes K, Geyer P. A test of inuslator interactions in Drosophila. EMBO J 2003; 22:2463-71; http://dx.doi.org/10.1093/emboj/cdg241
   PubMed Web of Science ®Google Scholar
• Henikoff S, Ahmed K, Malik H. The centromere paradox: stable inheritance with rapidly evolving DNA. Science 2001; 293:1098-102; PMID:11498581; http://dx.doi.org/10.1126/science.1062939
   PubMed Web of Science ®Google Scholar
• Abad JP, Agudo M, Molina I, Losada A, Ripoll P, Villasante A. Pericentromeric regions containing 1.688 satellite DNA sequences show anti-kinetochore antibody staining in prometaphase chromosomes of Drosophila melanogaster. Mol General Genet MGG 2000; 264:371-7; PMID:11129040; http://dx.doi.org/10.1007/s004380000331
   PubMedGoogle Scholar
• Larracuente AM. The organization and evolution of the Responder satellite in species of the Drosophila melanogaster group: dynamic evolution of a target of meiotic drive. BMC Evol Biol 2014; 14:233; http://dx.doi.org/10.1186/s12862-014-0233-9
   PubMed Web of Science ®Google Scholar