Koonin E.V., Zhou S., and Lucchesi J.C., 1995. The chromo superfamily: New members, duplication of the chromo domain and possible role in delivering transcription regulators to chromatin. Nucleic Acids Res. 23: 4229–4233.
Kuroda M.I., Keman M.J., KreberR., Ganetzky B., and Baker B.S., 1991. The maleless protein associates with the X chromosome to regulate dosage compensation in Drosophila. Cell 66: 935–947.
KuschT., Florens L., Macdonald W.H., Swanson S.K., Glaser R.L., Yates J.R., III, Abmayr S.M., Washburn M.R, and Workman J.L., 2004. Acetylation by Tip60 is required for selective histone variant exchange at DNA lesions. Science 306: 2084–2087.
Lee C.C., Chang K.A., Kurtoda M.I., and Hurwitz J., 1997. The NTPase/helicase activities of Drosophila maleless, an essential factor in dosage compensation. EMBO J. 16: 2671–2681.
Legube G., McWeeney S.K., Lercher M.J., and Akhtar A., 2006. X-chromosome-wide profiling of MSL-1 distribution and dosage compensation in Drosophila. Genes Dev., 20: 871–883.
Lucchesi J.C. and Manning J.E., 1987. Gene dosage compensation in Drosophila melanogaster. Adv. Genet. 24: 371–429.
Lucchesi J.C., Kelly W.G., and Panning B., 2005. Chromatin remodeling in dosage compensation. Annu. Rev. Genet. 39: 615–651.
Marin I., 2003. Evolution of chromatin-remodeling complexes: Comparative genomics reveals the ancient origin of “novel” compensasome genes. J. Mol. Evol. 56: 527–539.
Meller V.H. and Rattner B.P., 2002. The roXgenes encode redundant male-specific lethal transcripts required for targeting of the MSL complex. EMBO J. 21: 1084–1091.
Meller V.H., Wu K.H., Roman G., Kuroda M.L., and Davis R.L., 1997. roX1 RNA paints the X chromosome of male Drosophila and is regulated by the dosage compensation system. Cell 88: 445–457.
Meller V.H., Gordadze PR., Park Y., ChuX., Stuckenholz C., Kelley R.L., and Kuroda M.L., 2000. Ordered assembly of roX RNAs into MSL complexes on the dosage-compensated X chromosome in Drosophila. Curr. Biol. 10: 136–143.
Mendjan S., Taipale M., Kind J., Holz H., Gebhardt P., Schelder M., Verfneulen M., Buscaino A., Duncan K., Mueller J., et al., 20(56. Nuclear pore components are involved in the transcriptional regulation of dosage compensation in Drosophila. Mol. Cell 21: 811–823.
Mlito Y., Henikoff J.G., and Henikoff S., 2005. Genome-scale profiling of histone H3 3 replacement patterns. Nat. Genet. 37: 1090–1097.
Morales V., Straub X, Neumann M.F., Mengus G., Akhtar A., and Becker P.B., 2004. Functional integration of the histone acetyl-transferase MOF into the dosage compensation complex. EMBO J. 23: 2258–2268.
Morgan T.H., 1932. The scientific basis of evolution. Norton, New York, p. 80.
Oh H., Bone J.R., and Kuroda M.I., 2004. Multiple classes of MSL binding sites target dosage compensation to the X chromosome of Drosophila. Curr. Biol. 14: 481–487.
Oh H., Park Y., and Kuroda M.L, 2003. Local spreading of MSL complexes from roX genes on the Drosophda X chromosome. Genes Dev. 17: 1334–1339.
Palmer M.J., MergnerVA., Richman R., Manning J.E., Kuroda M.L, and Lucchesi J. C., 1993. The male-specific lethal-one (msi-1) gene of Drosophila melanogaster encodes a novel protein that associates with the X chromosome in males. Genetics 134: 545–557.
Pannuti A and Lucchesi J.C., 2000. Recycling to remodeclass="underline" Evolution ofdos-age-compensation complexes. Curr. Opm. Genet. Dev. 10: 644–650.
Pardo P.S., Leung J.K., Lucchesi J.C., and Pereira-Smith O.M., 2002. MRG15, a novel chromodomain protein, is present in two distinct multiprotein complexes involved in transcriptional activation. J. Biol. Chem. 277: 50860-50866.
Park Y., Kelley R.L., Oh H., Kuroda M.L., and Meller V.H., 2002. Extent of chromatin spreading determined by roX RNA recruitment of MSL proteins. Science 298: 1620-1623
Sass G.L., Pannuti A., and Lucchesi J.C.. 2003. Male-specific lethal complex of Drosophila targets activated regions ofthe X chromosome for chromatin remodeling. Proc. Natl. Acad. Sci. 100: 8287–8291.
Schalch T., Duda S., Sargent D.F., and Richmond T.J., 2005. X-ray structure of a tetranucleosome and its implications for the chromatin fibre. Nature 436: 138–141.
Scott M.J., Pan L.L., Cleland S.B., Knox A.L., and Heinrich J., 2000. MS LI plays a central role in assembly of the MSL complex, essential for dosage compensation in Drosophila. EMBO J.. 19: 144–155.
Sif S., 2004. ATP-dependent nucleosome remodeling complexes: Enzymes tailored to deal with chromatin. J. Cell Biochem. 91: 1087–1098.
Smith C.L. and Peterson C.L., 2005. ATP-dependent chromatin remodeling. Curr. Top. Dev. Biol. 65: 115–148.
Smith E.R., Allis C.D., and Lucchesi J.C., 2001. Linking global histone acetylation to the transcription enhancement of X-chromosomal genes in Drosophila males. J. Biol.Chem. 276: 31483-31486.
Smith E.R., Cayrou G., Huang R., Lane W.S., Cote J., and Lucchesi J.C., 2005. A human protein complex homologous to the Drosophila MSL complex is responsible for the majority of histone H4 acety-lation at lysine 16. Mol. Cell. Biol. 25: 9175–9188.
Smith E.R., Pannuti A., GuW., SteumagelA., Cook R.G., Allis C.D., and Lucchesi J.C., 2000. The Drosophila MSL complex acetylates histone H4 at lysine 16, a chromatin modification linked to dosage compensation. Mol. Cell. Biol., 20: 312-318
Smith E.R., Eisen A., GuW., Sattah M., Pannuti A., Zhou J., Cook R.G., Lucchesi J.C., and Allis C.D., 1998. ESA1 is a histone acetyltransferase that is essential for growth in yeast. Proc. Natl. Acad. Scl 95: 3561–3565.
Straub T., Dahlsveen I.K., and Becker P.B., 2005a. Dosage compensation in flies: Mechanism, models, mystery. FEBS Lett. 579: 3258–3263.
Straub T., Gilfillan C.D., Maier V.K., and Becker P.B., 2005b. The Drosophila MSL complex activates the transcription of target genes. Genes Dev., 19: 2284–2288.
Straub T., Neumann M.F., Prestel M., Kremmer E., Kaether C, Haass C, and Becker P.B., 2005c. Stable chromosomal association of MSL2 defines a dosage-compensated nuclear compartment. Chromosoma 114: 352–364.
Stuckenholz C, Meller V.H., and Kuroda M.L, 2003. Functional redundancy within roX1, a noncoding RNA involved in dosage compensation in Drosophila melanogaster. Genetics 164: 1003–1014.
Suka N., Luo K., and Grunstein M., 2002. Sir2p and Sas2p opposingly regulate acetylation of yeast histone H4 lysinel6 and spreading of heterochromatin. Nat. Genet. 32: 378–383.