The SR protein family of splicing factors: master regulators of gene expression

被引:867
作者
Long, Jennifer C. [1 ]
Caceres, Javier F. [1 ]
机构
[1] Western Gen Hosp, Inst Genet & Mol Med, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
alternative splicing; pre-mRNA splicing; RS domain; SR proteins; SR-related proteins; translation regulation; PRE-MESSENGER-RNA; SPINAL MUSCULAR-ATROPHY; U4/U6-CENTER-DOT-U5; TRI-SNRNP; SERINE/ARGININE-RICH PROTEINS; GENOME-WIDE SURVEY; SITE SELECTION; IN-VIVO; RS DOMAIN; PREMESSENGER RNA; FACTOR ASF/SF2;
D O I
10.1042/BJ20081501
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 SR protein family comprises a number of phylogenetically conserved and structurally related proteins with a characteristic domain rich in arginine and serine residues, known as the RS domain. They play significant roles ill constitutive pre-mRNA splicing and are also important regulators of alternative splicing. In addition they participate in post-splicing activities, such as mRNA nuclear export, nonsense-mediated ill RNA decay and mRNA translation. These wide-ranging roles of SR proteins highlight their importance as pivotal regulators of mRNA metabolism, and if these functions are disrupted, developmental defects or disease may result. Furthermore, animal models have shown a highly specific, non-redundant role for individual SR proteins in the regulation of developmental processes. Here, we will review the Current literature to demonstrate how SR proteins are emerging as one of the master regulators of gene expression.
引用
收藏
页码:15 / 27
页数:13
相关论文
共 215 条
[1]   THE SEX-DETERMINING GENE TRA-2 OF DROSOPHILA ENCODES A PUTATIVE RNA-BINDING PROTEIN [J].
AMREIN, H ;
GORMAN, M ;
NOTHIGER, R .
CELL, 1988, 55 (06) :1025-1035
[2]   Insights into the selective activation of alternatively used splice acceptors by the human immunodeficiency virus type-1 bidirectional splicing enhancer [J].
Asang, Corinna ;
Hauber, Ilona ;
Schaal, Heiner .
NUCLEIC ACIDS RESEARCH, 2008, 36 (05) :1450-1463
[3]   Small-molecule inhibition of HIV pre-mRNA splicing as a novel antiretroviral therapy to overcome drug resistance [J].
Bakkour, Nadia ;
Lin, Yea-Lih ;
Maire, Sophie ;
Ayadi, Lilia ;
Mahuteau-Betzer, Florence ;
Nguyen, Chi Hung ;
Mettling, Clement ;
Portales, Pierre ;
Grierson, David ;
Chabot, Benoit ;
Jeanteur, Philippe ;
Branlant, Christiane ;
Corbeau, Pierre ;
Tazi, Jamal .
PLOS PATHOGENS, 2007, 3 (10) :1530-1539
[4]   Highly active antiretroviral therapy: Current state of the art, new agents and their pharmacological interactions useful for improving therapeutic outcome [J].
Barbaro, G ;
Scozzafava, A ;
Mastrolorenzo, A ;
Supuran, CT .
CURRENT PHARMACEUTICAL DESIGN, 2005, 11 (14) :1805-1843
[5]   Regulation of alternative splicing by SRrp86 through coactivation and repression of specific SR proteins [J].
Barnard, DC ;
Li, J ;
Peng, R ;
Patton, JG .
RNA, 2002, 8 (04) :526-533
[6]   Stimulating full-length SMN2 expression by delivering bifunctional RNAs via a viral vector [J].
Baughan, Travis ;
Shababi, Monir ;
Coady, Tristan H. ;
Dickson, Alexa M. ;
Tullis, Gregory E. ;
Lorson, Christian L. .
MOLECULAR THERAPY, 2006, 14 (01) :54-62
[7]   SPLICING OF BALBIANI RING-1 GENE PREMESSENGER RNA OCCURS SIMULTANEOUSLY WITH TRANSCRIPTION [J].
BAUREN, G ;
WIESLANDER, L .
CELL, 1994, 76 (01) :183-192
[8]   A nucleo-cytoplasmic SR protein functions in viral IRES-mediated translation initiation [J].
Bedard, Kristin M. ;
Daijogo, Sarah ;
Semler, Bert L. .
EMBO JOURNAL, 2007, 26 (02) :459-467
[9]   Molecular cloning of htra2-beta-1 and htra2-beta-2, two human homologs of tra-2 generated by alternative splicing [J].
Beil, B ;
Screaton, G ;
Stamm, S .
DNA AND CELL BIOLOGY, 1997, 16 (06) :679-690
[10]   SPLICED SEGMENTS AT 5' TERMINUS OF ADENOVIRUS 2 LATE MESSENGER-RNA [J].
BERGET, SM ;
MOORE, C ;
SHARP, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (08) :3171-3175