Nonsense-mediated messenger RNA decay is initiated by endonucleolytic cleavage in Drosophila

被引:183
作者
Gatfield, D [1 ]
Izaurralde, E [1 ]
机构
[1] European Mol Biol Lab, D-69117 Heidelberg, Germany
关键词
D O I
10.1038/nature02559
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In eukaryotic cells, messenger RNAs harbouring premature termination codons (PTCs) are rapidly degraded by a conserved post-transcriptional mechanism referred to as nonsense-mediated mRNA decay (NMD)(1,2), which prevents the synthesis of truncated proteins that could be deleterious for the cell(1,2). Studies in yeast and mammals indicate that degradation by means of this pathway can occur from both the 5' end of the message (involving decapping and 5'-to-3' exonucleolytic digestion by XRN1) or the 3' end (through accelerated deadenylation and exosome-mediated 3'-to-5' decay)(3-9). Here we show that, contrary to expectation, degradation of PTC-containing messages in Drosophila is initiated by endonucleolytic cleavage(s) in the vicinity of the nonsense codon. The resulting 5' fragment is rapidly degraded by exonucleolytic digestion by the exosome, whereas the 3' fragment is degraded by XRN1. This decay route is shown for several PTC-containing reporters, as well as an endogenous mRNA that is naturally regulated by NMD. We conclude that, despite conservation in the NMD machinery, PTC-containing transcripts are degraded in Drosophila by a mechanism that differs considerably from those described in yeast and mammals(3,6,7).
引用
收藏
页码:575 / 578
页数:4
相关论文
共 30 条
[11]   Nonsense-mediated mRNA decay in Drosophila:: at the intersection of the yeast and mammalian pathways [J].
Gatfield, D ;
Unterholzner, L ;
Ciccarelli, FD ;
Bork, P ;
Izaurralde, E .
EMBO JOURNAL, 2003, 22 (15) :3960-3970
[12]  
HAGAN KW, 1995, MOL CELL BIOL, V15, P809
[13]   Cleavage of the A site mRNA codon during ribosome pausing provides a mechanism for translational quality control [J].
Hayes, CS ;
Sauer, RT .
MOLECULAR CELL, 2003, 12 (04) :903-911
[14]   Upf1p, Nmd2p, and Upf3p regulate the decapping and exonucleolytic degradation of both nonsense-containing mRNAs and wild-type mRNAs [J].
He, F ;
Jacobson, A .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (05) :1515-1530
[15]   The Drosophila gene for antizyme requires ribosomal frameshifting for expression and contains an intronic gene for snRNP Sm D3 on the opposite strand [J].
Ivanov, IP ;
Simin, K ;
Letsou, A ;
Atkins, JF ;
Gesteland, RF .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (03) :1553-1561
[16]   Purification and characterization of a polysome-associated endoribonuclease that degrades c-myc mRNA in vitro [J].
Lee, CH ;
Leeds, P ;
Ross, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (39) :25261-25271
[17]   Nonsense-mediated mRNA decay in mammalian cells involves decapping, deadenylating, and exonucleolytic activities [J].
Lejeune, F ;
Li, XJ ;
Maquat, LE .
MOLECULAR CELL, 2003, 12 (03) :675-687
[18]   HUMAN BETA-GLOBIN MESSENGER-RNAS THAT HARBOR A NONSENSE CODON ARE DEGRADED IN MURINE ERYTHROID TISSUES TO INTERMEDIATES LACKING REGIONS OF EXON-I OR EXON-I AND EXON-II THAT HAVE A CAP-LIKE STRUCTURE AT THE 5' TERMINI [J].
LIM, SK ;
MAQUAT, LE .
EMBO JOURNAL, 1992, 11 (09) :3271-3278
[19]   An NMD pathway in yeast involving accelerated deadenylation and exosome-mediated 3′→5′ degradation [J].
Mitchell, P ;
Tollervey, D .
MOLECULAR CELL, 2003, 11 (05) :1405-1413
[20]   PREMATURE TRANSLATIONAL TERMINATION TRIGGERS MESSENGER-RNA DECAPPING [J].
MUHLRAD, D ;
PARKER, R .
NATURE, 1994, 370 (6490) :578-581