Expression of metazoan replication-dependent histone genes

被引:49
作者
Jaeger, S
Barends, S
Giegé, R
Eriani, G
Martin, F
机构
[1] CNRS, Inst Biol Mol & Cellulaire, UPR 9002, Dept Mecanismes & Macromol Synth Prot & Cristallo, F-67084 Strasbourg, France
[2] Leiden Univ, Dept Biochem, NL-2300 RA Leiden, Netherlands
关键词
cell cycle-dependent histone; replication-dependent histone; histone mRNA metabolism; histone biogenesis;
D O I
10.1016/j.biochi.2005.03.012
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
Histone proteins are essential components of eukaryotic chromosomes. In metazoans, they are produced from the so-called replication-dependent histone genes. The biogenesis of histones is tightly coupled to DNA replication in a stoichiometric manner because an excess of histones is highly toxic for the cell. Therefore, a strict cell cycle-regulation of critical factors required for histone expression ensures exclusive S-phase expression. This review focuses on the molecular mechanisms responsible for such a fine expression regulation. Among these, a large part will be dedicated to post-transcriptional events occurring on histone mRNA, like histone mRNA 3' end processing, nucleo-cytoplasmic mRNA export, translation and mRNA degradation. Many factors are involved, including an RNA-binding protein called HBP, also called SLBP (for hairpin- or stem-loop-binding protein) that binds to a conserved hairpin located in the 3' UTR part of histone mRNA. HBP plays a pivotal role in the expression of histone genes since it is necessary for most of the steps of histone mRNA metabolism in the cell. Moreover, the strict S-phase expression pattern of histones is achieved through a fine cell cycle-regulation of HBP. A large part of the discussion will be centered on the critical role of HBP in histone biogenesis. (C) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:827 / 834
页数:8
相关论文
共 63 条
[1]   The stem-loop binding protein (SLBP1) is present in coiled bodies of the Xenopus germinal vesicle [J].
Abbott, J ;
Marzluff, WF ;
Gall, JG .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (02) :487-499
[2]   Cotranscriptional processing of Drosophila histone mRNAs [J].
Adamson, TE ;
Price, DH .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (12) :4046-4055
[3]   The stem-loop binding protein forms a highly stable and specific complex with the 3′ stem-loop of histone mRNAs [J].
Battle, DJ ;
Doudna, JA .
RNA, 2001, 7 (01) :123-132
[4]   Functional characterization of a human histone gene cluster duplication [J].
Braastad, CD ;
Hovhannisyan, H ;
van Wijnen, AJ ;
Stein, JL ;
Stein, GS .
GENE, 2004, 342 (01) :35-40
[5]   Crystallographic structure of the nuclease domain of 3′hExo, a DEDDh family member, bound to rAMP [J].
Cheng, Y ;
Patel, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 343 (02) :305-312
[6]   AN INTACT HISTONE 3'-PROCESSING SITE IS REQUIRED FOR TRANSCRIPTION TERMINATION IN A MOUSE HISTONE H2A GENE [J].
CHODCHOY, N ;
PANDEY, NB ;
MARZLUFF, WF .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (01) :497-509
[7]   CHANGES IN HISTONE GENE DOSAGE ALTER TRANSCRIPTION IN YEAST [J].
CLARKADAMS, CD ;
NORRIS, D ;
OSLEY, MA ;
FASSLER, JS ;
WINSTON, F .
GENES & DEVELOPMENT, 1988, 2 (02) :150-159
[8]   NMR structure and dynamics of the RNA-binding site for the histone mRNA stem-loop binding protein [J].
DeJong, ES ;
Marzluff, WF ;
Nikonowicz, EP .
RNA, 2002, 8 (01) :83-96
[9]   Formation of the 3′ end of histone mRNA [J].
Dominski, Z ;
Marzluff, WF .
GENE, 1999, 239 (01) :1-14
[10]  
Dominski Z, 1995, RNA, V1, P915