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An RNA code for the FOX2 splicing regulator revealed by mapping RNA-protein interactions in stem cells
被引:442
作者:
Yeo, Gene W.
[1
,2
,3
]
Coufal, Nicole G.
[3
]
Liang, Tiffany Y.
[2
]
Peng, Grace E.
[3
]
Fu, Xiang-Dong
Gage, Fred H.
[3
]
机构:
[1] Univ Calif San Diego, Dept Cellular & Mol Med, Stem Cell Program, La Jolla, CA 92093 USA
[2] Salk Inst Biol Studies, Crick Jacobs Ctr Theoret & Computat Biol, La Jolla, CA 92037 USA
[3] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
基金:
美国国家卫生研究院;
关键词:
CYTOFLUOROMETRIC ANALYSIS;
GENOME-WIDE;
DIFFERENTIATION;
IDENTIFICATION;
VERTEBRATE;
ENHANCERS;
SEQUENCES;
HOMOLOGS;
ELEMENTS;
DNA;
D O I:
10.1038/nsmb.1545
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The elucidation of a code for regulated splicing has been a long-standing goal in understanding the control of post-transcriptional gene expression events that are crucial for cell survival, differentiation and development. We decoded functional RNA elements in vivo by constructing an RNA map for the cell type-specific splicing regulator FOX2 (also known as RBM9) via cross-linking immunoprecipitation coupled with high-throughput sequencing (CLIP-seq) in human embryonic stem cells. The map identified a large cohort of specific FOX2 targets, many of which are themselves splicing regulators, and comparison between the FOX2 binding profile and validated splicing events revealed a general rule for FOX2-regulated exon inclusion or skipping in a positiondependent manner. These findings suggest that FOX2 functions as a critical regulator of a splicing network, and we further show that FOX2 is important for the survival of human embryonic stem cells.
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页码:130 / 137
页数:8
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