Control of RNA processing by a large non-coding RNA over-expressed in carcinomas

被引:75
作者
Lin, Rui [1 ]
Roychowdhury-Saha, Manami [1 ]
Black, Chris [2 ]
Watt, Andrew T. [2 ]
Marcusson, Eric G. [2 ]
Freier, Susan M. [2 ]
Edgington, Thomas S. [1 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
[2] ISIS Pharmaceut, Carlsbad, CA 92008 USA
来源
FEBS LETTERS | 2011年 / 585卷 / 04期
关键词
Hepcarcin; Sigma RNA/MALAT-1; RNA processing; Alternative splicing; TISSUE FACTOR GENE; CANCER; CELLS; METASTASIS; SEQUENCE; ENDOGLIN; MALAT-1;
D O I
10.1016/j.febslet.2011.01.030
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
RNA processing is vital for the high fidelity and diversity of eukaryotic transcriptomes and the encoded proteomes. However, control of RNA processing is not fully established. Sigma RNA is a class of conserved large non-coding RNAs (murine Hepcarcin; human MALAT-1) up-regulated in carcinomas. Using antisense technology, we identified that RNA post-transcriptional modification is the most significant global function of Sigma RNA. Specifically, processing of the pre-mRNAs of genes including Tissue Factor and Endoglin was altered by hydrolysis of Sigma RNA/MALAT-1. These results support the hypothesis that Sigma RNA/MALAT-1 is a regulatory molecule exerting roles in RNA post-transcriptional modification. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:671 / 676
页数:6
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