Genome-wide transcriptome analysis in murine neural retina using high-throughput RNA sequencing

被引:34
作者
Gamsiz, Ece D. [1 ]
Ouyang, Qing [1 ]
Schmidt, Michael [1 ]
Nagpal, Shailender [1 ]
Morrow, Eric M. [1 ]
机构
[1] Brown Univ, Dept Mol Biol Cell Biol & Biochem, Mol Med Lab, Providence, RI 02903 USA
关键词
Retina; Transcriptome; RNA-seq; Mouse; Alternative splicing; GENE-EXPRESSION ANALYSIS; MICROARRAY ANALYSIS; IDENTIFICATION; PROSPECTS; SEQ;
D O I
10.1016/j.ygeno.2011.09.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Genome-wide characterization of the retinal transcriptome is central to understanding development, physiology and disorders of the visual system. Massively parallel, short-read sequencing of mRNA libraries was used to generate an extensive map of the transcriptome of the adult, murine neural retina. RNA-seq data strongly corroborates prior transcriptome studies by microarray and SAGE. However, several novel features of the retinal transcriptome were discovered. For example, retinal disease genes were discovered to be among the most highly expressed in the transcriptome. We also demonstrate other interesting features of the retinal transcriptome, for example, that the retina appears to employ a very specific and restricted set of synaptic vesicle genes, and also that there is persistence of expression of a majority of "neurodevelopmental" genes into adulthood. Retina transcriptome studies utilizing novel sequencing methods have been highly informative and these data may also serve as a resource for the community of researchers. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:44 / 51
页数:8
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