Recruitment of the Puf3 protein to its mRNA target for regulation of mRNA decay in yeast

被引:65
作者
Jackson, JS [1 ]
Houshmandi, SS [1 ]
Leban, FL [1 ]
Olivas, WM [1 ]
机构
[1] Univ Missouri, Dept Biol, St Louis, MO 63121 USA
关键词
decay; turnover; mRNA; Puf; yeast; 3 ' UTR;
D O I
10.1261/rna.7270204
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
The Puf family of RNA-binding proteins regulates mRNA translation and decay via interactions with 3' untranslated regions (3, UTRs) of target mRNAs. In yeast, Puf3p binds the 3' UTR of COX17 mRNA and promotes rapid deadenylation and decay. We have investigated the sequences required for Puf3p recruitment to this 3' UTR and have identified two separate binding sites. These sites are specific for Puf3p, as they cannot bind another Puf protein, Puf5p. Both sites use a conserved UGUANAUA sequence, whereas one site contains additional sequences that enhance binding affinity. In vivo, presence of either site partially stimulates COX17 mRNA decay, but full decay regulation requires the presence of both sites. No other sequences outside the 3' UTR are required to mediate this decay regulation. The Puf repeat domain of Puf3p is sufficient not only for in vitro binding to the 3' UTR, but also in vivo stimulation of COX17 mRNA decay. These experiments indicate that the essential residues involved in mRNA decay regulation are wholly contained within this RNA-binding domain.
引用
收藏
页码:1625 / 1636
页数:12
相关论文
共 47 条
[1]   Pumilio homologue from Saprolegnia parasitica specifically expressed in undifferentiated spore cysts [J].
Andersson, MG ;
Cerenius, L .
EUKARYOTIC CELL, 2002, 1 (01) :105-111
[2]   Maternal Pumilio acts together with Nanos in germline development in Drosophila embryos [J].
Asaoka-Taguchi, M ;
Yamada, M ;
Nakamura, A ;
Hanyu, K ;
Kobayashi, S .
NATURE CELL BIOLOGY, 1999, 1 (07) :431-437
[3]   Purification, characterization, and localization of yeast Cox17p, a mitochondrial copper shuttle [J].
Beers, J ;
Glerum, DM ;
Tzagoloff, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (52) :33191-33196
[4]   A SMALL SEGMENT OF THE MAT-ALPHA-1 TRANSCRIPT PROMOTES MESSENGER-RNA DECAY IN SACCHAROMYCES-CEREVISIAE - A STIMULATORY ROLE FOR RARE CODONS [J].
CAPONIGRO, G ;
MUHLRAD, D ;
PARKER, R .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (09) :5141-5148
[5]   Poly(A)-independent regulation of maternal hunchback translation in the Drosophila embryo [J].
Chagnovich, D ;
Lehmann, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (20) :11359-11364
[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]   A CCHC metal-binding domain in Nanos is essential for translational regulation [J].
Curtis, D ;
Treiber, DK ;
Tao, F ;
Zamore, PD ;
Williamson, JR ;
Lehmann, R .
EMBO JOURNAL, 1997, 16 (04) :834-843
[8]   A TURNOVER PATHWAY FOR BOTH STABLE AND UNSTABLE MESSENGER-RNAS IN YEAST - EVIDENCE FOR A REQUIREMENT FOR DEADENYLATION [J].
DECKER, CJ ;
PARKER, R .
GENES & DEVELOPMENT, 1993, 7 (08) :1632-1643
[9]  
Derrigo M, 2000, INT J MOL MED, V5, P111
[10]   Structure of Pumilio reveals similarity between RNA and peptide binding motifs [J].
Edwards, TA ;
Pyle, SE ;
Wharton, RP ;
Aggarwal, AK .
CELL, 2001, 105 (02) :281-289