The complexity of the mammalian transcriptome

被引:78
作者
Gustincich, Stefano
Sandelin, Albin
Plessy, Charles
Katayama, Shintaro
Simone, Roberto
Lazarevic, Dejan
Hayashizaki, Yoshihide
Carninci, Piero
机构
[1] SISSA, ISAS, Sector Neurobiol, I-34102 Trieste, Italy
[2] SISSA, ISAS, Giovanni Armenise Harvard Fdn Lab, I-34102 Trieste, Italy
[3] RIKEN, Yokohama Inst, Lab Genome Explorat, Res Grp,GSC,Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[4] RIKEN, Discovery & Res Inst, Genome Sci Lab, Wako Inst, Wako, Saitama 3510198, Japan
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2006年 / 575卷 / 02期
关键词
D O I
10.1113/jphysiol.2006.115568
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A comprehensive understanding of protein and regulatory networks is strictly dependent on the complete description of the transcriptome of cells. After the determination of the genome sequence of several mammalian species, gene identification is based on in silico predictions followed by evidence of transcription. Conservative estimates suggest that there are about 20 000 protein-encoding genes in the mammalian genome. In the last few years the combination of full-length cDNA cloning, cap-analysis gene expression (CAGE) tag sequencing and tiling arrays experiments have unveiled unexpected additional complexities in the transcriptome. Here we describe the current view of the mammalian transcriptome focusing on transcripts diversity, the growing non-coding RNA world, the organization of transcriptional units in the genome and promoter structures. In-depth analysis of the brain transcriptome has been challenging due to the cellular complexity of this organ. Here we present a computational analysis of CAGE data from different regions of the central nervous system, suggesting distinctive mechanisms of brain-specific transcription.
引用
收藏
页码:321 / 332
页数:12
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