The role of the DEAD-box RNA helicase DDX3 in mRNA metabolism

被引:106
作者
Soto-Rifo, Ricardo [1 ]
Ohlmann, Theophile [2 ,3 ,4 ,5 ,6 ]
机构
[1] Univ Chile, Fac Med, Inst Ciencias Biomed, Programa Virol, Santiago 7, Chile
[2] Univ Lyon, Int Ctr Infectiol Res, CIRI, Lyon, France
[3] INSERM, U1111, F-69008 Lyon, France
[4] Ecole Normale Super Lyon, F-69364 Lyon, France
[5] Univ Lyon 1, Ctr Int Rech Infectiol, F-69365 Lyon, France
[6] CNRS, UMR5308, Lyon, France
关键词
CORE PROTEIN INTERACTS; DEPENDENT TRANSLATION; CRYSTAL-STRUCTURE; CELL-GROWTH; ATPASE DDX3; IN-VITRO; EXPORT; COMPLEX; GENE; TARGET;
D O I
10.1002/wrna.1165
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
DDX3 belongs to the DEAD-box proteins, a large family of ATP-dependent RNA helicases that participate in all aspects of RNA metabolism. Human DDX3 is a component of several messenger ribonucleoproteins that are found in the spliceosome, the export and the translation initiation machineries but also in different cytoplasmic mRNA granules. DDX3 has been involved in several cellular processes such as cell cycle progression, apoptosis, cancer, innate immune response, and also as a host factor for viral replication. Interestingly, not all these functions require the catalytic activities of DDX3 and thus, the precise roles of this apparently multifaceted protein remain largely obscure. The aim of this review is to provide a rapid and critical overview of the structure and functions of DDX3 with a particular emphasis on its role during mRNA metabolism. WIREs RNA 2013, 4:369-385. doi: 10.1002/wrna.1165 Conflict of interest: The authors have declared no conflicts of interest for this article. For further resources related to this article, please visit the WIREs website.
引用
收藏
页码:369 / 385
页数:17
相关论文
共 115 条
[1]   Bypassing of stems versus linear base-by-base inspection of mammalian mRNAs during ribosomal scanning [J].
Abaeva, Irina S. ;
Marintchev, Assen ;
Pisareva, Vera P. ;
Hellen, Christopher U. T. ;
Pestova, Tatyana V. .
EMBO JOURNAL, 2011, 30 (01) :115-129
[2]   Inositol hexakisphosphate and Gle1 activate the DEAD-box protein Dbp5 for nuclear mRNA export [J].
Alcazar-Roman, Abel R. ;
Tran, Elizabeth J. ;
Guo, Shuangli ;
Wente, Susan R. .
NATURE CELL BIOLOGY, 2006, 8 (07) :711-U131
[3]   RNA granules [J].
Anderson, P ;
Kedersha, N .
JOURNAL OF CELL BIOLOGY, 2006, 172 (06) :803-808
[4]   Stress granules: The Tao of RNA triage [J].
Anderson, Paul ;
Kedersha, Nancy .
TRENDS IN BIOCHEMICAL SCIENCES, 2008, 33 (03) :141-150
[5]   RNA granules: post-transcriptional and epigenetic modulators of gene expression [J].
Anderson, Paul ;
Kedersha, Nancy .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (06) :430-436
[6]   Requirement of cellular DDX3 for hepatitis C virus replication is unrelated to its interaction with the viral core protein [J].
Angus, Allan G. N. ;
Dalrymple, David ;
Boulant, Steeve ;
McGivern, David R. ;
Clayton, Reginald F. ;
Scott, Martin J. ;
Adair, Richard ;
Graham, Susan ;
Owsianka, Ania M. ;
Targett-Adams, Paul ;
Li, Kui ;
Wakita, Takaji ;
McLauchlan, John ;
Lemon, Stanley M. ;
Patel, Arvind H. .
JOURNAL OF GENERAL VIROLOGY, 2010, 91 :122-132
[7]  
[Anonymous], PLOS ONE
[8]   DDX3 DEAD-box RNA helicase is required for hepatitis C virus RNA replication [J].
Ariumi, Yasuo ;
Kuroki, Misao ;
Abe, Ken-ichi ;
Dansako, Hiromichi ;
Ikeda, Masanori ;
Wakita, Takaji ;
Kato, Nobuyuki .
JOURNAL OF VIROLOGY, 2007, 81 (24) :13922-13926
[9]   The exon junction core complex is locked onto RNA by inhibition of eIF4AIII ATPase activity [J].
Ballut, L ;
Marchadier, B ;
Baguet, A ;
Tomasetto, C ;
Séraphin, B ;
Le Hir, H .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2005, 12 (10) :861-869
[10]   The DEAD-box RNA helicase Ded1p affects and accumulates in Saccharomyces cerevisiae P-bodies [J].
Beckham, Carla ;
Hilliker, Angela ;
Cziko, Anne-Marie ;
Noueiry, Amine ;
Ramaswami, Mani ;
Parker, Roy .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (03) :984-993