Massive translational repression of gene expression during mouse erythroid differentiation

被引:1
|
作者
Pradet-Balade, Berengere [1 ]
Leberbauer, Cornelia [2 ]
Schweifer, Norbert [3 ]
Boulme, Florence [2 ]
机构
[1] UAM, Dept Immunol & Oncol, Ctr Nacl Biotecnol CNB CSIC, Madrid 28049, Spain
[2] Med Univ Vienna, Dept Med Biochem, Div Mol Biol, Max F Perutz Labs,Univ Dept,Vienna Bioctr, A-1030 Vienna, Austria
[3] Boehringer Ingelheim Austria RCV GmbH Co & KG, A-1121 Vienna, Austria
关键词
Mouse erythroid differentiation; Translation regulation; Erythropoiesis; Microarray; MESSENGER-RNA TRANSLATION; INHIBITS DIFFERENTIATION; HEMATOPOIETIC-CELLS; SELF-RENEWAL; T-CELLS; TRANSFORMATION; PROLIFERATION; TRANSCRIPTION; MICROARRAYS; ACTIVATION;
D O I
10.1016/j.bbagrm.2010.08.006
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
We took advantage of a mouse erythroid differentiation system to determine the relative contribution of transcriptional and translational control during this process. Comparison of expression data obtained with total cytoplasmic mRNAs or polysome-bound mRNAs (actively translated mRNAs) on Affymetrix high-density oligonucleotide microarrays revealed different characteristics of the two regulatory mechanisms. Indeed, mRNA expression from a vast majority of genes was affected, albeit most changes were relatively small and occurred at a low pace. Translational control, however, affected a smaller fraction of genes but was effective at earlier time-points. This analysis unravels six clusters of genes showing no significant variation in mRNA expression levels whereas they are submitted to translational regulation. Their involvement in terminal mouse erythropoiesis may prove to be highly relevant. Furthermore, the data from specific and functional categories of genes emphasize that translational control, not only reinforces the transcriptional effect, but allows the cell to increase the complexity in gene expression regulation patterns. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:630 / 641
页数:12
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