Gene Expression - Time to Change Point of View?

被引:7
作者
Larsson, Ola [1 ,2 ,3 ]
Nadon, Robert [1 ,2 ,4 ]
机构
[1] McGill Univ, Montreal, PQ H3A 1A4, Canada
[2] Genome Quebec Innovat Ctr, Montreal, PQ H3A 1A4, Canada
[3] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[4] McGill Univ, Dept Human Genet, Montreal, PQ H3A 1B1, Canada
来源
BIOTECHNOLOGY AND GENETIC ENGINEERING REVIEWS, VOL 25 | 2008年 / 25卷
关键词
D O I
10.5661/bger-25-77
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
Analysis of transcription profiles has been the focus of genome wide characterization of gene expression during the last decade. Downstream of transcription, regulation of translation represents a less explored step in the gene expression pathway. Differential translation can be caused by differential ribosome recruitment, translational elongation or termination although the ribosome recruitment step is thought to be the major source of differential translation. Genome wide studies of differential translation through analysis of ribosome recruitment in a variety of model systems indicate better correlation to protein levels as compared to transcriptional regulation. These studies also indicate translational control as a major transcript specific regulation step. Here we review the current literature on genome wide regulation of ribosome recruitment. We conclude that without considering regulation of ribosome recruitment, important information regarding the links between gene expression and protein levels is lost and that ribosome recruitment will be an integral part of a systems level understanding for regulation of gene expression.
引用
收藏
页码:77 / 92
页数:16
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