In Search of a Function for BCLAF1

被引:55
作者
Sarras, Haya [1 ]
Azami, Solmaz Alizadeh [1 ]
McPherson, J. Peter [1 ]
机构
[1] Univ Toronto, Dept Pharmacol & Toxicol, Toronto, ON M5S 1A1, Canada
关键词
BCLAF1; apoptosis; transcription; RS domain; lung development; Kaposi's sarcoma; ribonucleoprotein; TRAP150; RNA transport; PRE-MESSENGER-RNA; PROMOTING TRANSCRIPTIONAL REPRESSOR; NUCLEAR RIBONUCLEOPROTEIN-H; DNA-SEQUENCES; LUNG DEVELOPMENT; PROTEIN; EMERIN; GENE; ACTIVATION; MULTIPLE;
D O I
10.1100/tsw.2010.132
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
BCLAF1 was originally identified as a protein that interacts with antiapoptotic members of the Bcl2 family. Initial studies indicated a role for this protein as an inducer of apoptosis and repressor of transcription. Subsequent studies have shown that BCLAF1 plays criticals roles in a wide range of processes that are not normally associated with actions of Bcl2 family members, including lung development, T-cell activation, and control of the lytic infection program of Kaposi's sarcoma-associated herpesvirus. Here, we provide an overview of findings from past studies that both support and challenge the role of BCLAF1 in cell death and transcriptional control. We also present recent findings from our laboratory and others indicating a role for BCLAF1 in post-transcriptional processes that impact mRNA metabolism, instead of a direct role for this protein in apoptosis or transcription.
引用
收藏
页码:1450 / 1461
页数:12
相关论文
共 67 条
[1]   Multiple and surprising new functions for emerin, a nuclear membrane protein [J].
Bengtsson, L ;
Wilson, KL .
CURRENT OPINION IN CELL BIOLOGY, 2004, 16 (01) :73-79
[2]   STRUCTURE OF ADENOVIRUS 2 EARLY MESSENGER-RNAS [J].
BERK, AJ ;
SHARP, PA .
CELL, 1978, 14 (03) :695-711
[3]   IDENTIFICATION OF A NOVEL X-LINKED GENE RESPONSIBLE FOR EMERY-DREIFUSS MUSCULAR-DYSTROPHY [J].
BIONE, S ;
MAESTRINI, E ;
RIVELLA, S ;
MANCINI, M ;
REGIS, S ;
ROMEO, G ;
TONIOLO, D .
NATURE GENETICS, 1994, 8 (04) :323-327
[4]   Mammary epithelial-mesenchymal interaction regulates fibronectin alternative splicing via phosphatidylinositol 3-kinase [J].
Blaustein, M ;
Pelisch, F ;
Coso, OA ;
Bissell, MJ ;
Kornblihtt, AR ;
Srebrow, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (20) :21029-21037
[5]   Aids-related malignancies [J].
Boshoff, C ;
Weiss, R .
NATURE REVIEWS CANCER, 2002, 2 (05) :373-382
[6]   Herpesvirus saimiri ORF57: a post-transcriptional regulatory protein [J].
Boyne, James R. ;
Colgan, Kevin J. ;
Whitehouse, Adrian .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2008, 13 :2928-2938
[7]   Recruitment of the Complete hTREX Complex Is Required for Kaposi's Sarcoma-Associated Herpesvirus Intronless mRNA Nuclear Export and Virus Replication [J].
Boyne, James R. ;
Colgan, Kevin J. ;
Whitehouse, Adrian .
PLOS PATHOGENS, 2008, 4 (10)
[8]   γ-2 Herpes virus post-transcriptional gene regulation [J].
Boyne, JR ;
Whitehouse, A .
CLINICAL MICROBIOLOGY AND INFECTION, 2006, 12 (02) :110-117
[9]   Regulation of cyclin D1 RNA stability by SNIP1 [J].
Bracken, Cameron P. ;
Wall, Steven J. ;
Barre, Benjamin ;
Panov, Kostya I. ;
Ajuh, Paul M. ;
Perkins, Neil D. .
CANCER RESEARCH, 2008, 68 (18) :7621-7628
[10]   Role of the modular domains of SR proteins in subnuclear localization and alternative splicing specificity [J].
Caceres, JF ;
Misteli, T ;
Screaton, GR ;
Spector, DL ;
Krainer, AR .
JOURNAL OF CELL BIOLOGY, 1997, 138 (02) :225-238