Helical repeats modular proteins are major players for organelle gene expression

被引:62
作者
Hammani, Kamel [1 ]
Bonnard, Geraldine [1 ]
Bouchoucha, Ayoub [1 ]
Gobert, Anthony [1 ]
Pinker, Franziska [1 ]
Salinas, Thalia [1 ]
Giege, Philippe [1 ]
机构
[1] CNRS, IBMP, UPR2357, F-67084 Strasbourg, France
关键词
Pentatricopeptide repeat; Octotricopeptide repeat; Half a tetratricopeptide; Mitochondrial transcription termination factor; Modular proteins; RNA-BINDING PROTEINS; MESSENGER-RNA; ARABIDOPSIS-THALIANA; PPR PROTEINS; TETRATRICOPEPTIDE REPEAT; MITOCHONDRIAL GENOME; TRYPANOSOMA-BRUCEI; FAMILY PROTEINS; NUCLEAR GENES; HUMAN HOMOLOG;
D O I
10.1016/j.biochi.2013.08.031
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
Mitochondria and chloroplasts are often described as semi-autonomous organelles because they have retained a genome. They thus require fully functional gene expression machineries. Many of the required processes going all the way from transcription to translation have specificities in organelles and arose during eukaryote history. Most factors involved in these RNA maturation steps have remained elusive for a long time. The recent identification of a number of novel protein families including pentatricopeptide repeat proteins, half-a-tetratricopeptide proteins, octotricopeptide repeat proteins and mitochondrial transcription termination factors has helped to settle long-standing questions regarding organelle gene expression. In particular, their functions have been related to replication, transcription, RNA processing, RNA editing, splicing, the control of RNA turnover and translation throughout eukaryotes. These families of proteins, although evolutionary independent, seem to share a common overall architecture. For all of them, proteins contain tandem arrays of repeated motifs. Each module is composed of two to three alpha-helices and their succession forms a super-helix. Here, we review the features characterising these protein families, in particular, their distribution, the identified functions and mode of action and propose that they might share similar substrate recognition mechanisms. (C) 2013 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:141 / 150
页数:10
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