Muscleblind-like 1 (Mbnl1) regulates pre-mRNA alternative splicing during terminal erythropoiesis

被引：43

作者：

Cheng, Albert W. ^{[1
,2
]}

Shi, Jiahai ^{[1
]}

Wong, Piu ^{[1
]}

Luo, Katherine L. ^{[3
,4
]}

Trepman, Paula ^{[3
,4
]}

Wang, Eric T. ^{[3
,4
,5
]}

Choi, Heejo ^{[3
,4
]}

Burge, Christopher B. ^{[3
,4
]}

Lodish, Harvey F. ^{[1
,3
,4
]}

机构：

[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA

[2] MIT, Computat & Syst Biol Program, Cambridge, MA 02142 USA

[3] MIT, Dept Biol, Cambridge, MA 02142 USA

[4] MIT, Dept Biol Engn, Cambridge, MA 02142 USA

[5] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA

来源：

BLOOD | 2014年 / 124卷 / 04期

基金：

美国国家卫生研究院;

关键词：

CYTOPLASMIC DYNEIN; GENE-EXPRESSION; PROTEINS; CELL; NDEL1; NUDEL; E2F4; LIS1; DIFFERENTIATION; LOCALIZATION;

D O I：

10.1182/blood-2013-12-542209

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

The scope and roles of regulated isoform gene expression during erythroid terminal development are poorly understood. We identified hundreds of differentiation-associated isoform changes during terminal erythropoiesis. Sequences surrounding cassette exons of skipped exon events are enriched for motifs bound by the Muscleblind-like (MBNL) family of splicing factors. Knockdown of Mbnl1 in cultured murine fetal liver erythroid progenitors resulted in a strong block in erythroid differentiation and disrupted the developmentally regulated exon skipping of Ndel1 mRNA, which is bound by MBNL1 and critical for erythroid terminal proliferation. These findings reveal an unanticipated scope of the alternative splicing program and the importance of Mbnl1 during erythroid terminal differentiation.

引用

页码：598 / 610

页数：13

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