De novo DNA methyltransferases DNMT3A and DNMT3B are essential for XIST silencing for erosion of dosage compensation in pluripotent stem cells-Reference-Cited by-同舟云学术

De novo DNA methyltransferases DNMT3A and DNMT3B are essential for XIST silencing for erosion of dosage compensation in pluripotent stem cells

Published:2021-09 Issue:9 Volume:16 Page:2138-2148
ISSN:2213-6711
Container-title:Stem Cell Reports
language:en
Short-container-title:Stem Cell Reports

Author:

Fukuda Atsushi,Hazelbaker Dane Z.,Motosugi Nami,Hao Jin,Limone Francesco,Beccard Amanda,Mazzucato Patrizia,Messana Angelica,Okada Chisa,San Juan Irune Guerra,Qian Menglu,Umezawa Akihiro,Akutsu Hidenori,Barrett Lindy E.,Eggan Kevin

Funder

Broad Institute

Japan Society for the Promotion of Science

National Institute of General Medical Sciences

Japan Agency for Medical Research and Development

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology,Genetics,Biochemistry

Reference30 articles.

1. Molecular signatures of human induced pluripotent stem cells highlight sex differences and cancer genes;Anguera;Cell Stem Cell,2012

2. Regulation of X-chromosome inactivation by the X-inactivation centre;Augui;Nat. Rev. Genet.,2011

3. Differentially methylated CpG island within human XIST mediates alternative P2 transcription and YY1 binding;Chapman;BMC Genet.,2014

4. 5-Azacytidine and 5-aza-2'-deoxycytidine as inhibitors of DNA methylation: mechanistic studies and their implications for cancer therapy;Christman;Oncogene,2002

5. Synergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivation;Csankovszki;J. Cell Biol.,2001

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