A 3′ UTR sequence stabilizes termination codons in the unspliced RNA of Rous sarcoma virus

被引:68
作者
Weil, JE [1 ]
Beemon, KL [1 ]
机构
[1] Johns Hopkins Univ, Dept Biol, Baltimore, MD 21218 USA
关键词
NMD; RNA surveillance; translation termination; Rous sarcoma virus;
D O I
10.1261/rna.2129806
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
Eukaryotic cells target mRNAs to the nonsense-mediated mRNA decay (NMD) pathway when translation terminates within the coding region. In mammalian cells, this is presumably due to a downstream signal deposited during pre-mRNA splicing. In contrast, unspliced retroviral RNA undergoes NMD in chicken cells when premature termination codons (PTCs) are present in the gag gene. Surprisingly, deletion of a 401 -nt 3' UTR sequence immediately downstream of the normal gag termination codon caused this termination event to be recognized as premature. We termed this 3' UTR region the Rous sarcoma virus (RSV) stability element (RSE). The RSE also stabilized the viral RNA when placed immediately downstream of a PTC in the gag gene. Deletion analysis of the RSE indicated a smaller functional element. We conclude that this 3' UTR sequence stabilizes termination codons in the RSV RNA, and termination codons not associated with such an RSE sequence undergo NMD.
引用
收藏
页码:102 / 110
页数:9
相关论文
共 56 条
[1]   A faux 3′-UTR promotes aberrant termination and triggers nonsense-mediated mRNA decay [J].
Amrani, N ;
Ganesan, R ;
Kervestin, S ;
Mangus, DA ;
Ghosh, S ;
Jacobson, A .
NATURE, 2004, 432 (7013) :112-118
[2]   ROUS-SARCOMA VIRUS-RNA STABILITY REQUIRES AN OPEN READING FRAME IN THE GAG GENE AND SEQUENCES DOWNSTREAM OF THE GAG-POL JUNCTION [J].
BARKER, GF ;
BEEMON, K .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (03) :1986-1996
[3]   NONSENSE CODONS WITHIN THE ROUS-SARCOMA VIRUS GAG GENE DECREASE THE STABILITY OF UNSPLICED VIRAL-RNA [J].
BARKER, GF ;
BEEMON, K .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (05) :2760-2768
[4]   EVIDENCE TO IMPLICATE TRANSLATION BY RIBOSOMES IN THE MECHANISM BY WHICH NONSENSE CODONS REDUCE THE NUCLEAR-LEVEL OF HUMAN TRIOSEPHOSPHATE ISOMERASE MESSENGER-RNA [J].
BELGRADER, P ;
CHENG, J ;
MAQUAT, LE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) :482-486
[5]   Splicing of human immunodeficiency virus RNA is position-dependent suggesting sequential removal of introns from the 5′ end [J].
Bohne, J ;
Wodrich, H ;
Kräusslich, HG .
NUCLEIC ACIDS RESEARCH, 2005, 33 (03) :825-837
[6]   The human intronless melanocortin 4-receptor gene is NMD insensitive [J].
Brocke, KS ;
Neu-Yilik, G ;
Gehring, NH ;
Hentze, MW ;
Kulozik, AE .
HUMAN MOLECULAR GENETICS, 2002, 11 (03) :331-335
[7]   Transcriptional silencing of nonsense codon-containing immunoglobulin minigenes [J].
Bühler, M ;
Mohn, F ;
Stalder, L ;
Mühlemann, O .
MOLECULAR CELL, 2005, 18 (03) :307-317
[8]   Efficient downregulation of immunoglobulin μ mRNA with premature translation-termination codons requires the 5′-half of the VDJ exon [J].
Bühler, M ;
Paillusson, A ;
Mühlemann, O .
NUCLEIC ACIDS RESEARCH, 2004, 32 (11) :3304-3315
[9]   Infrequent translation of a nonsense codon is sufficient to decrease mRNA level [J].
Buzina, A ;
Shulman, MJ .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (03) :515-524
[10]   A splicing-dependent regulatory mechanism that detects translation signals [J].
Carter, MS ;
Li, SL ;
Wilkinson, MF .
EMBO JOURNAL, 1996, 15 (21) :5965-5975