Upf1p, Nmd2p, and Upf3p regulate the decapping and exonucleolytic degradation of both nonsense-containing mRNAs and wild-type mRNAs

被引:75
作者
He, F [1 ]
Jacobson, A [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Microbiol & Mol Genet, Worcester, MA 01655 USA
关键词
D O I
10.1128/MCB.21.5.1515-1530.2001
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
In Saccharomyces cerevisiae, rapid degradation of nonsense containing mRNAs requires the decapping enzyme Dcp1p, the 5'-to-3' exoribonuclease Xrn1p, and the three nonsense-mediated mRNA decay (NMD) factors, Upf1p, Nmd2p, and Upf3p. To identify specific functions for the NMD factors, we analyzed the mRNA decay phenotypes of yeast strains containing deletions of DCP1 or XRN1 and UPF1, NMD2, or UPF3. Our results indicate that Upf1p, Nmd2p, and Upf3p regulate decapping and exonucleolytic degradation of nonsense-containing mRNAs. In addition,we show that these factors also regulate the same processes in the degradation of wild-type mRNAs. The participation of the NMD factors in general mRNA degradation suggests that they may regulate an aspect of translation termination common to all transcripts.
引用
收藏
页码:1515 / 1530
页数:16
相关论文
共 73 条
[1]   NAM7 NUCLEAR GENE ENCODES A NOVEL MEMBER OF A FAMILY OF HELICASES WITH A ZN-LIGAND MOTIF AND IS INVOLVED IN MITOCHONDRIAL FUNCTIONS IN SACCHAROMYCES-CEREVISIAE [J].
ALTAMURA, N ;
GROUDINSKY, O ;
DUJARDIN, G ;
SLONIMSKI, PP .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 224 (03) :575-587
[2]   ISOLATION AND CHARACTERIZATION OF RAT1 - AN ESSENTIAL GENE OF SACCHAROMYCES-CEREVISIAE REQUIRED FOR THE EFFICIENT NUCLEOCYTOPLASMIC TRAFFICKING OF MESSENGER-RNA [J].
AMBERG, DC ;
GOLDSTEIN, AL ;
COLE, CN .
GENES & DEVELOPMENT, 1992, 6 (07) :1173-1189
[3]  
[Anonymous], METHOD ENZYMOL
[4]   Relationship between yeast polyribosomes and Upf proteins required for nonsense mRNA decay [J].
Atkin, AL ;
Schenkman, LR ;
Eastham, M ;
Dahlseid, JN ;
Lelivelt, MJ ;
Culbertson, MR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (35) :22163-22172
[5]  
ATKIN AL, 1995, MOL BIOL CELL, V6, P611
[6]   DEGRADATION OF MESSENGER-RNA IN EUKARYOTES [J].
BEELMAN, CA ;
PARKER, R .
CELL, 1995, 81 (02) :179-183
[7]   An essential component of the decapping enzyme required for normal rates of mRNA turnover [J].
Beelman, CA ;
Stevens, A ;
Caponigro, G ;
LaGrandeur, TE ;
Hatfield, L ;
Fortner, DM ;
Parker, R .
NATURE, 1996, 382 (6592) :642-646
[8]   Overexpression of truncated Nmd3p inhibits protein synthesis in yeast [J].
Belk, JP ;
He, F ;
Jacobson, A .
RNA, 1999, 5 (08) :1055-1070
[9]   THE EFFICIENCY OF TRANSLATION TERMINATION IS DETERMINED BY A SYNERGISTIC INTERPLAY BETWEEN UPSTREAM AND DOWNSTREAM SEQUENCES IN SACCHAROMYCES-CEREVISIAE [J].
BONETTI, B ;
FU, LW ;
MOON, J ;
BEDWELL, DM .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 251 (03) :334-345
[10]   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