Deletion of the PAT1 gene affects translation initiation and suppresses a PAB1 gene deletion in yeast

被引:49
作者
Wyers, F [1 ]
Minet, M [1 ]
Dufour, ME [1 ]
Vo, LTA [1 ]
Lacroute, F [1 ]
机构
[1] CNRS, Ctr Genet Mol, F-91198 Gif Sur Yvette, France
关键词
D O I
10.1128/MCB.20.10.3538-3549.2000
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 yeast poly(A) binding protein Pab1p mediates the interactions between the 5' cap structure and the 3' poly(A) tail of mRNA, whose structures synergistically activate translation in vivo and in vitro. We found that deletion of the PAT1 (YCR077c) gene suppresses a PAB1 gene deletion and that Pat1p is required for the normal initiation of translation. A fraction of Pat1p cosediments with free 40S ribosomal subunits on sucrose gradients. The PAT1 gene is not essential for viability, although disruption of the gene severely impairs translation initiation in vivo, resulting in the accumulation of 80S ribosomes and in a large decrease in the amounts of heavier polysomes. Pat1p contributes to the efficiency of translation in a yeast cell-free system. However, the synergy between the cap structure and the poly(A) tail is maintained in vitro in the absence of Pat1p, Analysis of translation initiation intermediates on gradients indicates that Pat1p acts at a step before or during the recruitment of the 40S ribosomal subunit by the mRNA, a step which may be independent of that involving Pab1p. We conclude that Pat1p is a new factor involved in protein synthesis and that Pat1p might be required for promoting the formation or the stabilization of the preinitiation translation complexes.
引用
收藏
页码:3538 / 3549
页数:12
相关论文
共 53 条
[1]   PCF11 encodes a third protein component of yeast cleavage and polyadenylation factor I [J].
Amrani, N ;
Minet, M ;
Wyers, F ;
Dufour, ME ;
Aggerbeck, LP ;
Lacroute, F .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (03) :1102-1109
[2]   Yeast Pab1 interacts with Rna15 and participates in the control of the poly(A) tail length in vitro [J].
Amrani, N ;
Minet, M ;
LeGouar, M ;
Lacroute, F ;
Wyers, F .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (07) :3694-3701
[3]  
[Anonymous], 1988, Antibodies: A Laboratory Manual
[4]   EVIDENCE FOR TRANSCRIPTIONAL REGULATION OF OROTIDINE-5'-PHOSPHATE DECARBOXYLASE IN YEAST BY HYBRIDIZATION OF MESSENGER-RNA TO THE YEAST STRUCTURAL GENE CLONED IN ESCHERICHIA-COLI [J].
BACH, ML ;
LACROUTE, F ;
BOTSTEIN, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (01) :386-390
[5]   Capped mRNA degradation intermediates accumulate in the yeast spb8-2 mutant [J].
Boeck, R ;
Lapeyre, B ;
Brown, CE ;
Sachs, AB .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (09) :5062-5072
[6]   Poly(A) tail length control in Saccharomyces cerevisiae occurs by message-specific deadenylation [J].
Brown, CE ;
Sachs, AB .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6548-6559
[7]   Mechanisms and control of mRNA turnover in Saccharomyces cerevisiae [J].
Caponigro, G ;
Parker, R .
MICROBIOLOGICAL REVIEWS, 1996, 60 (01) :233-+
[8]   MULTIPLE FUNCTIONS FOR POLY(A)-BINDING PROTEIN IN MESSENGER-RNA DECAPPING AND DEADENYLATION IN YEAST [J].
CAPONIGRO, G ;
PARKER, R .
GENES & DEVELOPMENT, 1995, 9 (19) :2421-2432
[9]   mRNA stabilization by poly(A) binding protein is independent of poly(A) and requires translation [J].
Coller, JM ;
Gray, NK ;
Wickens, MP .
GENES & DEVELOPMENT, 1998, 12 (20) :3226-3235
[10]   The DCP2 protein is required for mRNA decapping in Saccharomyces cerevisiae and contains a functional MutT motif [J].
Dunckley, T ;
Parker, R .
EMBO JOURNAL, 1999, 18 (19) :5411-5422