3′ UTRs Are the Primary Regulators of Gene Expression in the C-elegans Germline

被引:280
作者
Merritt, Christopher [1 ]
Rasoloson, Dominique [1 ]
Ko, Darae [1 ]
Seydoux, Geraldine [1 ]
机构
[1] Johns Hopkins Sch Med, Dept Mol Biol & Genet, Howard Hughes Med Inst, Ctr Cell Dynam, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.cub.2008.08.013
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
How genes are regulated to produce the correct assortment of proteins for every cell type is a fundamental question in biology. For many genes, regulation begins at the DNA level with the use of promoter sequences to control transcription. Regulation can also occur after transcription using sequences in the 3' untranslated region (UTR) of the mRNA to affect mRNA stability and/or translation [1]. The C. elegans gonad is an excellent tissue to study gene regulation during development: In the adult, germ cells are arranged in order of differentiation, with undifferentiated progenitors at one end of the gonad, cells in meiotic prophase in the middle, and gametes at the other end [2]. Using a transgenic assay, we have compared the contribution of promoters and 3' UTRs to gene regulation during germline development. We find that for most genes tested, 3' UTRs are sufficient for regulation. With the exception of promoters activated during spermatogenesis, promoters are permissive for expression in all germ cell types (from progenitors to oocytes and sperm). In progenitors, 3' UTRs inhibit the production of meiotic and oocyte proteins by posttranscriptional mechanisms involving PUF- and KH-domain RNA-binding proteins. Our findings indicate that many genes rely primarily on 3' UTRs, not promoters, for regulation during germline development.
引用
收藏
页码:1476 / 1482
页数:7
相关论文
共 31 条
[1]   Binding specificity and mRNA targets of a C-elegans PUF protein, FBF-1 [J].
Bernstein, D ;
Hook, B ;
Hajarnavis, A ;
Opperman, L ;
Wickens, M .
RNA, 2005, 11 (04) :447-458
[2]   Revealing posttranscriptional regulatory elements through network-level conservation [J].
Chan, g S. Chan ;
Elemento, Olivier ;
Tavazoie, Saeed .
PLOS COMPUTATIONAL BIOLOGY, 2005, 1 (07) :564-578
[3]  
Chi Woo, 2006, Development, V133, P3147, DOI 10.1242/dev.02490
[4]   Translational regulators maintain totipotency in the Caenorhabditis elegans germline [J].
Ciosk, R ;
DePalma, M ;
Priess, JR .
SCIENCE, 2006, 311 (5762) :851-853
[5]   ATX-2, the C-elegans ortholog of ataxin 2, functions in translational regulation in the germline [J].
Ciosk, R ;
DePalma, M ;
Priess, JR .
DEVELOPMENT, 2004, 131 (19) :4831-4841
[6]   A conserved RNA-binding protein controls germline stem cells in Caenorhabditis elegans [J].
Crittenden, SL ;
Bernstein, DS ;
Bachorik, JL ;
Thompson, BE ;
Gallegos, M ;
Petcherski, AG ;
Moulder, G ;
Barstead, R ;
Wickens, M ;
Kimble, J .
NATURE, 2002, 417 (6889) :660-663
[7]   Translational repression restricts expression of the C-elegans Nanos homolog NOS-2 to the embryonic germline [J].
D'Agostino, I ;
Merritt, C ;
Chen, PL ;
Seydoux, G ;
Subramaniam, K .
DEVELOPMENTAL BIOLOGY, 2006, 292 (01) :244-252
[8]   Mechanisms of translational control by the 3′ UTR in development and differentiation [J].
de Moor, CH ;
Meijer, H ;
Lissenden, S .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2005, 16 (01) :49-58
[9]   A universal framework for regulatory element discovery across all Genomes and data types [J].
Elemento, Olivier ;
Slonim, Noam ;
Tavazoie, Saeed .
MOLECULAR CELL, 2007, 28 (02) :337-350
[10]  
ELLIS R, 2007, WORMBOOK C ELEGANS R, DOI DOI 10.1895/WORMBOOK.1.82.2