[1]Amir RE, Van den Veyver IB, Wan M, et al. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2[J]. Nature Genetics, 1999, 23:185-188. [2]Gitschier J. On the Track of DNA Methylation:An Interview with adrian bird[J]. PLoS Genet, 2009, 5(10):e1000667. [3]Chen RZ, Akbarian S, Tudor M, Jaenisch R . Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice[J]. Nature Genetics, 2001, 27:327-331. [4]Guy J, Hendrich B, Holmes M, et al. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome[J]. Nature Genetics, 2001, 27:322-326. [5]Weng AP, Ferrando AA, Lee W, et al. Activating mutations of Notch1 in human T cell acute lymphoblastic leukemia[J]. Science, 2004, 306(5694):269-271. [6]Radtke F, Schweisguth F, Pear W. The Notch ‘gospel’-workshop on notch signalling in development and cancer[J]. EMBO Reports, 2005, 6(12):1120-1125. [7]De Strooper B, Annaert W, Cupers P. A presenilin-1-dependent r-secretase-like protease mediates release of Notch intraCellular domain[J]. Nature, 1999, 398(6727):518-522. [8]Iso T, Kedes L, Hamamori Y. HES and HERP families:multiple effectors of the Notch signaling pathway[J]. Journal of Cellular Physiology, 2003, 194(3):237-255. [9] Gao H, Bu Y, Wang X, et al. Mecp2 regulates neural cell differentia-tion by suppressing the Id1-Her2/Hes5 axis in zebrafish[J]. Journal of Cell Science, 2015, 128(12):2340-2350. [10] Louvi A, Artavanis-Tsakonas S. Notch signalling in vertebrate neural development[J]. Nature Reviews Neuroscience, 2006, 7(2):93-102. [11] Fortini ME. Notch Signaling:The core pathway and its posttrans-lational regulation[J]. Developmental Cell, 2009, 16(3):633-647. [12]Kishi N, Macklis JD. MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions[J]. Molecular and Cellular Neuroscience, 200, 27:306-321. [13] Li Y, Wang H, Muffat J, et al. Global transcriptional and translati-onal repression in human-embryonic-stem-cell-derived rett syndro-me neurons[J]. Cell Stem Cell, 2013, 13:446-458. [14]Chahrour M, Jung SY, Shaw C, et al. Mecp2, a key contributor to neurological disease, activates and represses transcription[J]. Science, 2008, 320:1224-1229. [15]Young JI, Hong EP, Castle JC, et al. Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2[J]. Proc Natl Acad Sci USA, 2005, 102:17551-17558. [16]Long SW, Ooi JY, Yau PM, Jones PL. A brain-derived Mecp2 complex supports a role for Mecp2 in RNA processing[J]. Bioscience Reports, 2011, 31:333-343. |