A Pooled shRNA Screen Identifies Rbm15, Spen, and Wtap as Factors Required for Xist RNA-Mediated Silencing

被引:197
作者
Moindrot, Benoit [1 ]
Cerase, Andrea [1 ]
Coker, Heather [1 ]
Masui, Osamu [3 ]
Grijzenhout, Anne [1 ]
Pintacuda, Greta [1 ]
Schermelleh, Lothar [2 ]
Nesterova, Tatyana B. [1 ]
Brockdorff, Neil [1 ]
机构
[1] Univ Oxford, Dept Biochem, Dev Epigenet, Oxford OX1 3QU, England
[2] Univ Oxford, Dept Biochem, Adv Cellular Imaging, Oxford OX1 3QU, England
[3] RIKEN Ctr Integrat Med Sci, Lab Dev Genet, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
来源
CELL REPORTS | 2015年 / 12卷 / 04期
基金
英国惠康基金;
关键词
INACTIVE X-CHROMOSOME; SUPERRESOLUTION MICROSCOPY; CELLS; PROTEINS; METHYLATION; BINDING; GENE; LOCALIZATION; EFFICIENCY; REVEALS;
D O I
10.1016/j.celrep.2015.06.053
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
X-chromosome inactivation is the process that evolved in mammals to equalize levels of X-linked gene expression in XX females relative to XY males. Silencing of a single X chromosome in female cells is mediated by the non-coding RNA Xist. Although progress has been made toward identifying factors that function in the maintenance of X inactivation, the primary silencing factors are largely undefined. We developed an shRNA screening strategy to produce a ranked list of candidate primary silencing factors. Validation experiments performed on several of the top hits identified the SPOC domain RNA binding proteins Rbm15 and Spen and Wtap, a component of the m6A RNA methyltransferase complex, as playing an important role in the establishment of Xist-mediated silencing. Localization analysis using super-resolution 3D-SIM microscopy demonstrates that these factors co-localize with Xist RNA within the nuclear matrix subcompartment, consistent with a direct interaction.
引用
收藏
页码:562 / 572
页数:11
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