The exosome contains domains with specific endoribonuclease, exoribonuclease and cytoplasmic mRNA decay activities

被引:226
作者
Schaeffer, Daneen [1 ]
Tsanova, Borislava [1 ]
Barbas, Ana [2 ]
Reis, Filipa Pereira [2 ]
Dastidar, Eeshita Ghosh [1 ]
Sanchez-Rotunno, Maya [1 ]
Arraiano, Cecilia Maria [2 ]
van Hoof, Ambro [1 ]
机构
[1] Univ Texas Houston, Hlth Sci Ctr, Dept Microbiol & Mol Genet, Houston, TX 77030 USA
[2] Univ Nova Lisboa, Inst Tecnol Quim & Biol, P-2781901 Oeiras, Portugal
基金
美国国家卫生研究院;
关键词
ESCHERICHIA-COLI; YEAST EXOSOME; SACCHAROMYCES-CEREVISIAE; RIBOSOMAL-RNA; ARCHAEAL EXOSOME; RIBONUCLEASE-II; PIN-DOMAIN; CRYSTAL-STRUCTURE; STRUCTURAL BASIS; DEGRADATION;
D O I
10.1038/nsmb.1528
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 eukaryotic exosome is a ten-subunit 3' exoribonucleolytic complex responsible for many RNA-processing and RNA-degradation reactions. How the exosome accomplishes this is unknown. Rrp44 (also known as Dis3), a member of the RNase II family of enzymes, is the catalytic subunit of the exosome. We show that the PIN domain of Rrp44 has endoribonucleolytic activity. The PIN domain is preferentially active toward RNA with a 5' phosphate, suggesting coordination of 5' and 3' processing. We also show that the endonuclease activity is important in vivo. Furthermore, the essential exosome subunit Csl4 does not contain any domains that are required for viability, but its zinc-ribbon domain is required for exosome-mediated mRNA decay. These results suggest that specific exosome domains contribute to specific functions, and that different RNAs probably interact with the exosome differently. The combination of an endoRNase and an exoRNase activity seems to be a widespread feature of RNA-degrading machines.
引用
收藏
页码:56 / 62
页数:7
相关论文
共 59 条
[1]   The yeast exosome and human PM-Scl are related complexes of 3′→5′ exonucleases [J].
Allmang, C ;
Petfalski, E ;
Podtelejnikov, A ;
Mann, M ;
Tollervey, D ;
Mitchell, P .
GENES & DEVELOPMENT, 1999, 13 (16) :2148-2158
[2]   Functions of the exosome in rRNA, snoRNA and snRNA synthesis [J].
Allmang, C ;
Kufel, J ;
Chanfreau, G ;
Mitchell, P ;
Petfalski, E ;
Tollervey, D .
EMBO JOURNAL, 1999, 18 (19) :5399-5410
[3]   A single mutation in Escherichia coli ribonuclease II inactivates the enzyme without affecting RNA binding [J].
Amblar, M ;
Arraiano, CM .
FEBS JOURNAL, 2005, 272 (02) :363-374
[4]   Characterization of the functional domains of Escherichia coli RNase II [J].
Amblar, Monica ;
Barbas, Ana ;
Fialho, Arsenio M. ;
Arraiano, Cecilia M. .
JOURNAL OF MOLECULAR BIOLOGY, 2006, 360 (05) :921-933
[5]   The 3′ to 5′ degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3′ to 5′ exonucleases of the exosome complex [J].
Anderson, JSJ ;
Parker, R .
EMBO JOURNAL, 1998, 17 (05) :1497-1506
[6]  
ANDRADE JM, PROG NUCL A IN PRESS
[7]   A role for eIF4E and eIF4E-transporter in targeting mRNPs to mammalian processing bodies [J].
Andrei, MA ;
Ingelfinger, D ;
Heintzmann, R ;
Achsel, T ;
Rivera-Pomar, R ;
Lührmann, R .
RNA, 2005, 11 (05) :717-727
[8]   Distant structural homology leads to the functional characterization of an archaeal PIN domain as an exonuclease [J].
Arcus, VL ;
Bäckbro, K ;
Roos, A ;
Daniel, EL ;
Baker, EN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (16) :16471-16478
[9]   New insights into the mechanism of RNA degradation by ribonuclease II -: Identification of the residue responsible for setting the RNase II end product [J].
Barbas, Ana ;
Matos, Rute G. ;
Amblar, Monica ;
Lopez-Vinas, Eduardo ;
Gomez-Puertas, Paulino ;
Arraiano, Cecilia M. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (19) :13070-13076
[10]   A mouse cytoplasmic exoribonuclease (mXRN1p) with preference for G4 tetraplex substrates [J].
Bashkirov, VI ;
Scherthan, H ;
Solinger, JA ;
Buerstedde, JM ;
Heyer, WD .
JOURNAL OF CELL BIOLOGY, 1997, 136 (04) :761-773