Destroy this message after reading it!;Détruisez ce message (ARN) après l'avoir lu!

Medecine/Sciences

Volumn 23, Issue 10, 2007, Pages 850-856

  Camier, Sylvie ^a   Séraphin, Bertrand ^a  

^a CENTRE DE GÉNÉTIQUE MOLÉCULAIRE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA;

GENE CONTROL; GENE EXPRESSION; PROTEIN FUNCTION; PROTEIN STABILITY; QUALITY CONTROL; REVIEW;

EID: 35548933291     PISSN: 07670974     EISSN: None     Source Type: Journal    
DOI: 10.1051/medsci/20072310850     Document Type: Review

References (39)

1. th ed. New York : Garland Science, 2002.
2. Meyer S, Temme C, Wahle E. Messenger RNA turnover in eukaryotes: pathways and enzymes. Crit Rev Biochem Mol Biol 2004 ; 39 : 197-216.
3. Garneau NL, Wilusz J, Wilusz CJ. The highways and byways of mRNA decay. Nat Rev Mol Cell Biol 2007 ; 8 : 113-26.
4. Brown CE, Sachs AB. Poly(A) tail length control in Soccharomyces cerevisiae occurs by message-specific deadenylation. Mol Cell Biol 1998 ; 18 : 6548-59.
5. Yamashita A, Chang TC, Yamashita Y, et al. Concerted action of poly(A) nucleases and decapping enzyme in mammalian mRNA turnover. Nat Struct Mol Biol 2005 ; 12 : 1054-63.
6. Daugeron MC, Mauxion F, Seraphin B. The yeast POP2 gene encodes a nuclease involved in mRNA deadenylation. Nucleic Acids Res 2001 ; 29 : 2448-55.
7. Finoux AL, Seraphin B. In vivo targeting of the yeast Pop2 deadenylase subunit to reporter transcripts induces their rapid degradation and generates new decay intermediates. J Biol Chem 2006 ; 281 : 25940-7.
8. Tucker M, Staples RR, Valencia-Sanchez MA, et al. Ccr4p is the catalytic subunit of a Ccr4p/Pop2p/Notp mRNA deadenylase complex in Soccharomyces cerevisiae. EMBO J 2002 ; 21 : 1427-36.
9. Bianchin C, Mauxion F, Sentis S, et al. Conservation of the deadenylase activity of proteins of the Caf1 family in human. RNA 2005 ; 11 : 487-94.
10. Cougot N, van Dijk E, Babajko S, Seraphin B. Cap-tabolism. Trends Biochem Sci 2004 ; 29 : 436-44.
11. Simon E, Comier S, Seraphin B. New insights into the control of mRNA decapping. Trends Biochem Sci 2006 ; 31 : 241-3.
12. Mitchell P, Petfalski E, Shevchenko A, et al. The exosome: a conserved eukaryotic RNA processing complex containing multiple 3′-<5′ exoribonucleases. Cell 1997 ; 91 : 457-66.
13. Buttner K, Wenig K, Hopfner KP. The exosome: a macromolecular cage for controlled RNA degradation. Mol Microbiol 2006 ; 61 : 1372-9.
14. Dziembowski A, Lorentzen E, Conti E, Seraphin B. A single subunit, Dis3, is essentially responsible for yeast exosome core activity. Nat Struct Mol Biol 2007 ; 14 : 15-22.
15. Liu H, Rodgers ND, Jiao X, Kiledjian M. The scavenger mRNA decapping enzyme DcpS is a member of the HIT family of pyrophosphatases. EMBO J 2002 ; 21 : 4699-708.
16. Van Dijk E, Le Hir H, Seraphin B. DcpS can act in the 5′-3′ mRNA decay pathway in addition to the 3′-5′ pathway. Proc Natl Acad Sci USA 2003 ; 100 : 12081-6.
17. Cougot N, Babajko S, Seraphin B. Cytoplasmic foci are sites of mRNA decay in human cells. J Cell Biol 2004 ; 165 : 31-40.
18. Eulalio A, Behm-Ansmant I, Izaurralde E. P bodies: at the crossroads of post-transcriptional pathways. Nat Rev Mol Cell Biol 2007 ; 8 : 9-22.
19. Parker R, Sheth U. P bodies and the control of mRNA translation and degradation. Mol Cell 2007 ; 25 : 635-46.
20. Olesen JR, Libri D, Jensen TH. A link between transcription and mRNP quality in Soccharomyces cerevisiae. RNA Biol 2005 ; 2 : 45-8.
21. Kadaba S, Krueger A, Trice T, et al. Nuclear surveillance and degradation of hypomodified initiator tRNAMet in S. cerevisiae. Genes Dev 2004 ; 18 : 1227-40.
22. Wyers F, Rougemaille M, Badis G, et al. Cryptic pol II transcripts are degraded by a nuclear quality control pathway involving a new poly(A) polymerase. Cell 2005 ; 121 : 725-37.
23. LaCava J, Houseley J, Saveanu C, et al. RNA degradation by the exosome is promoted by a nuclear polyadenylation complex. Cell 2005 ; 121 : 713-24.
24. Amrani N, Sachs MS, Jacobson A. Early nonsense: mRNA decay solves a translational problem. Nat Rev Mol Cell Biol 2006 ; 7 : 415-25.
25. Le Hir H, Moore MJ, Maquat LE. Pre-mRNA splicing alters mRNP composition: evidence for stable association of proteins at exon-exon junctions. Genes Dev 2000 ; 14 : 1098-108.
26. Vasudevan S, Peltz SW, Wilusz CJ. Non-stop decay: a new mRNA surveillance pathway. Bioessays 2002 ; 24 : 785-8.
27. Doma MK, Parker R. Endonucleolytic cleavage of eukaryotic mRNAs with stalls in translation elongation. Nature 2006 ; 440 : 561-4.
28. Brengues M, Teixeira D, Parker R. Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies. Science 2005 ; 310 : 486-9.
29. Cheadle C, Fan J, Cho-Chung YS, et al. Control of gene expression during T cell activation: alternate regulation of mRNA transcription and mRNA stability. BMC Genomics 2005 ; 6 : 75.
30. Wickens M, Bernstein DS, Kimble J, Parker R. A PUF family portrait: 3'UTR regulation as a way of life. Trends Genet 2002 ; 18 : 150-7.
31. Goldstrohm AC, Hook BA, Seay DJ, Wickens M. PUF proteins bind Pop2p to regulate messenger RNAs. Nat Struct Mol Biol 2006 ; 13 : 533-9.
32. Barreau C, Paillard L, Osborne HB. AU-rich elements and associated factors: are there unifying principles? Nucleic Acids Res 2005 ; 33 : 7138-50.
33. Lykke-Andersen J, Wagner E. Recruitment and activation of mRNA decay enzymes by two ARE-mediated decay activation domains in the proteins TTP and BRF-1. Genes Dev 2005 ; 19 : 351-61.
34. Peng SS, Chen CY, Xu N, Shyu AB. RNA stabilization by the AU-rich element binding protein, HuR, an ELAV protein. EMBO J 1998 ; 17 : 3461-70.
35. Tang G. siRNA and miRNA: an insight into RISCs. Trends Biochem Sci 2005 ; 30 : 106-14.
36. Parker JS, Barford D. Argonaute: a scaffold for the function of short regulatory RNAs. Trends Biochem Sci 2006 ; 31 : 622-30.
37. Rana TM. Illuminating the silence: understanding the structure and function of small RNAs. Nat Rev Mol Cell Biol 2007 ; 8 : 23-36.
38. Samuel CE. Antiviral actions of interferons. Clin Microbiol Rev 2001 ; 14 : 778-809.
39. Harel-Bellan A. Prix Nobel de Médecine à Andrew Z. Fire et Craig c. Mello : silence, on désactive les gènes. Med Sci (Paris) 2006 ; 22 : 993-4.