RNA-guided assembly of Rev-RRE nuclear export complexes

被引:72
作者
Bai, Yun [1 ]
Tambe, Akshay [1 ]
Zhou, Kaihong [1 ,2 ]
Doudna, Jennifer A. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Phys Biosci Div, Berkeley, CA 94720 USA
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; SELECTIVE 2'-HYDROXYL ACYLATION; SECONDARY STRUCTURE PREDICTION; SINGLE-NUCLEOTIDE RESOLUTION; RESPONSE ELEMENT; HIV-1; REV; MESSENGER-RNA; VIRION EXPRESSION; SHAPE CHEMISTRY; GENE-EXPRESSION;
D O I
10.7554/eLife.03656
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
HIV replication requires nuclear export of unspliced and singly spliced viral transcripts. Although a unique RNA structure has been proposed for the Rev-response element (RRE) responsible for viral mRNA export, how it recruits multiple HIV Rev proteins to form an export complex has been unclear. We show here that initial binding of Rev to the RRE triggers RNA tertiary structural changes, enabling further Rev binding and the rapid formation of a viral export complex. Analysis of the Rev-RRE assembly pathway using SHAPE-Seq and small-angle X-ray scattering (SAXS) reveals two major steps of Rev-RRE complex formation, beginning with rapid Rev binding to a pre-organized region presenting multiple Rev binding sites. This step induces long-range remodeling of the RNA to expose a cryptic Rev binding site, enabling rapid assembly of additional Rev proteins into the RNA export complex. This kinetic pathway may help maintain the balance between viral replication and maturation.
引用
收藏
页码:1 / 17
页数:17
相关论文
共 65 条
[1]
Concurrent nucleation of 16S folding and induced fit in 30S ribosome assembly [J].
Adilakshmi, Tadepalli ;
Bellur, Deepti L. ;
Woodson, Sarah A. .
NATURE, 2008, 455 (7217) :1268-1272
[2]
Aviran Sharon, 2011, 2011 49th Annual Allerton Conference on Communication, Control, and Computing (Allerton), P1743
[3]
Modeling and automation of sequencing-based characterization of RNA structure [J].
Aviran, Sharon ;
Trapnell, Cole ;
Lucks, Julius B. ;
Mortimer, Stefanie A. ;
Luo, Shujun ;
Schroth, Gary P. ;
Doudna, Jennifer A. ;
Arkin, Adam P. ;
Pachter, Lior .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (27) :11069-11074
[4]
Hepatitis C virus 3′UTR regulates viral translation through direct interactions with the host translation machinery [J].
Bai, Yun ;
Zhou, Kaihong ;
Doudna, Jennifer A. .
NUCLEIC ACIDS RESEARCH, 2013, 41 (16) :7861-7874
[5]
alpha helix-RNA major groove recognition in an HIV-1 Rev peptide RRE RNA complex [J].
Battiste, JL ;
Mao, HY ;
Rao, NS ;
Tan, RY ;
Muhandiram, DR ;
Kay, LE ;
Frankel, AD ;
Williamson, JR .
SCIENCE, 1996, 273 (5281) :1547-1551
[6]
Crystal Structure of the HCV IRES Central Domain Reveals Strategy for Start-Codon Positioning [J].
Berry, Katherine E. ;
Waghray, Shruti ;
Mortimer, Stefanie A. ;
Bai, Yun ;
Doudna, Jennifer A. .
STRUCTURE, 2011, 19 (10) :1456-1466
[7]
The role of dynamic conformational ensembles in biomolecular recognition [J].
Boehr, David D. ;
Nussinov, Ruth ;
Wright, Peter E. .
NATURE CHEMICAL BIOLOGY, 2009, 5 (11) :789-796
[8]
Two distinct binding modes of a protein cofactor with its target RNA [J].
Bokinsky, Gregory ;
Nivon, Lucas G. ;
Liu, Shixin ;
Chai, Geqing ;
Hong, Minh ;
Weeks, Kevin M. ;
Zhuang, Xiaowei .
JOURNAL OF MOLECULAR BIOLOGY, 2006, 361 (04) :771-784
[9]
Identification of a regulated pathway for nuclear pre-mRNA turnover [J].
Bousquet-Antonelli, C ;
Presutti, C ;
Tollervey, D .
CELL, 2000, 102 (06) :765-775
[10]
Rev proteins of human and simian immunodeficiency virus enhance RNA encapsidation [J].
Brandt, Sabine ;
Blissenbach, Maik ;
Grewe, Bastian ;
Konietzny, Rebecca ;
Grunwald, Thomas ;
Ueberla, Klaus .
PLOS PATHOGENS, 2007, 3 (04) :518-525