Эпигенетика: читать книгу онлайн полностью и бесплатно

Bird A.P and Wolffe A.P., 1999. Methylation-induced repression — Belts, braces and chromatin. Cell 99: 451–454.

Bird A., Taggart M., Frommer M., Miller O.J., and Macleod D., 1985 A fraction of the mouse genome that is derived from islands of non-methylated, CpG-rich DNA. Cell 40: 91–99.

Bourc’his D. and Bestor T.H., 2004. Meiotic catastrophe and retrotrans-poson reactivation in male germ cells lacking Dnmt3L. Nature 431: 96–99.

Boyes J. and Bird A., 1991. DNA methylation inhibits transcription indirectly via a methyl-CpG-binding protein. Cell 64: 1123–1134.

Brandeis M., Frank D., Keshet I., Siegried Z., Mendelsohn M., Nemes A., TemperV.,RazinA., and Cedar H., 1994. Spl elements protect a CpG island from de novo methylation. Nature 371: 435–438.

Bruniquel D. and Schwartz R.H., 2003. Selective, stable demethylation of the interleukin-2 gene enhances transcription by an active process. Nat. Immunol. 4: 235–240.

Buschhausen G., Wittig B., Graessmann M., and Graessmann A., 1987. Chromatin structure is required to block transcription of the methylated herpes simplex virus thymidine kinase gene. Proc. Natl. Acad. Sci. 84: 1177–1181.

Chen R.Z., Akbarian S., Tudor M., and Jaenisch R., 2001. Deficiency of methyl-CpG-binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nat. Genet. 27: 327–331.

Chen W.G., Chang Q., Lin Y., Meissner A., West A.E., Griffith E.C., Jaenisch R., and Greenberg M.E., 2003. Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2. Science 302: 885–889.

Cooney C.A., Dave A.A., and Wolff G.L., 2002. Maternal methyl supplements in mice affect epigenetic variation and DNA methylation of offspring. J. Nutr. 132: 2393S-2400S.

Cooper D.N. and Youssoufian H., 1988. The CpG dinucleotide and human genetic disease. Hum. Genet. 78: 151–155.

Cooper D.N., Taggart M.H., and Bird A.P., 1983. Unmethylated domains invertebrate DNA. Nucleic Acids Res. 11: 647–658.

Dennis K., Fan T., Geiman T., Yan Q., and Muegge K., 2001. Lsh. a member of the SNF2 family, is required for genome-wide methylation. Genes Dev. 15: 2940–2944.

Dodge J.E., Okano M., Dick R., Tsujimoto N., Chen T., Wang S., Ueda Y., Dyson N., and Li E., 2005. Inactivation of Dnmt3b in mouse embryonic fibroblasts results in DNA hypomethylation, chromosomal instability, and spontaneous immortalization. J. Biol. Chem. 280: 17986-17991.

Egger G., Liang G., Aparicio A., and Jones P.A., 2004. Epigenetics in human disease and prospects for epigenetic therapy. Nature 429: 457–463.

Ehrlich M., 1982. Amount and distribution of 5-methycytosine in human DNA from different types of tissues or cells. Nucleic Acids Res. 10: 2709–2721.

Ehrlich M., 2003. The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease. Clin. Immunol. 109: 17–28.

Frank D., Keshet I., Shani M., Levine A., Razin A., and Cedar H., 1991. Demethylation of CpG islands in embryonic cells. Nature 351: 239–241.

Frommer M., McDonald L.E., Millar D.S., Collis C.M., Watt J., Grigg G.W., Molloy P.L., and Paul C.L., 1992. A genomic sequencing protocol that yields a positive display of 5-methyl-cytosine residues in individual DNA strands. Proc. Natl. Acad. Sci. 89: 1827–1831.

Gaudet E., Hodgson J.G., Eden A., Jackson-Grusby L., Dausman J., Gray J.W., Leonhardt H., and Jaenisch R., 2003. Induction of tumors in mice by genomic hypomethylation. Science 300: 489–492.

Gibbons R.J., McDowell XL., Raman S., O’Rourke D.M., Garrick D., Ayyub H., and Higgs D.R., 2000. Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation. Nat. Genet. 24: 368–371.

Guy J., Hendrich B., Holmes M., Martin J.E., and Bird A., 2001. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Nat. Genet. 27: 322–326.

Harbers K., Schnieke H., Stuhlmann H., Jahner D., and Jaenisch B., 1981. DNA methylation and gene expression; endogenous retroviral genome becomes infectious after molecular cloning. Proc. Natl. Acad. Sci. 78: 7609–7613.

Hata K., Okano M., Lei H., and Li E., 2002. Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice. Development 129: 1983–1993.

Hendrich B., Guy J., Ramsahoye B., Wilson V. A., and Bird A., 2001. Closely related proteins Mbd2 and Mbd3 play distinctive but interacting roles in mouse development. Genes Dev. 15: 710–723.

Hendrich B., Hardeland U., Ng H.-H., Jiricny J., and Bird A., 1999. The thymine glycosylase MBD4 can bind to the product of deamination at methylated CpG sites. Nature 401: 301–304.

Herman J.G., Graff J.R., Myohanen S., Nelkin B.D., and Baylin S.B., 1996. Methylation-specific PCR: A novel PCR assay for methylation status of CpG islands. Proc. Natl. Acad. Sci. 93: 9821–9826.

Holliday R. and Pugh J.E., 1975. DNA modification mechanisms and gene activity during development. Science 186: 226–232.

Hutchins A., Mullen A., Lee H., Barner K., High E, Hendrich B., Bird A., and Reiner S., 2002. Gene silencing quantitatively controls the function of a developmental trans-activator. Mol. Cell 10: 81–91.

Jackson J.P., Lindroth A.M., Cao X., and Jacobsen S.E., 2002. Control of CpNpG DNA methylation by the KRYPTONITE histone H3 methyltransferase. Nature 416: 556–560.