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HIV-1 splicing is controlled by local RNA structure and binding of splicing regulatory proteins at the major 5' splice site
被引:16
作者:
Mueller, Nancy
[1
]
Berkhout, Ben
[1
]
Das, Atze T.
[1
]
机构:
[1] Univ Amsterdam, Acad Med Ctr, Lab Expt Virol, Dept Med Microbiol,Ctr Infect & Immun Amsterdam C, NL-1012 WX Amsterdam, Netherlands
关键词:
PRE-MESSENGER-RNA;
INHERITED DEMENTIA FTDP-17;
SPINAL MUSCULAR-ATROPHY;
SURVIVAL MOTOR-NEURON;
SECONDARY STRUCTURE;
GENE-EXPRESSION;
SILENCER ELEMENT;
CRITICAL EXON;
U1;
SNRNA;
SR;
D O I:
10.1099/vir.0.000122
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
The 5' leader region of the human immunodeficiency virus 1 (HIV-1) RNA genome contains the major 5' splice site (ss) that is used in the production of the many spliced viral RNAs. This splice-donor (SD) region can fold into a stable stem loop structure and the thermodynamic stability of this RNA hairpin influences splicing efficiency. In addition, splicing may be modulated by binding of splicing regulatory (SR) proteins, in particular SF2/ASF (SRSF1), SC35 (SRSF2), SRp40 (SRSF5) and SRp55 (SRSF6), to sequence elements in the SD region. The role of RNA structure and SR protein binding in splicing control was previously studied by functional analysis of mutant SD sequences. The interpretation of these studies was complicated by the fact that most mutations simultaneously affect both structure and sequence elements. We therefore tried to disentangle the contribution of these two variables by designing more precise SD region mutants with a single effect on either the sequence or the structure. The current analysis indicates that HIV-1 splicing at the major 5'ss is modulated by both the stability of the local RNA structure and the binding of splicing regulatory proteins.
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页码:1906 / 1917
页数:12
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