Promoter usage and alternative splicing

被引:169
作者
Kornblihtt, AR [1 ]
机构
[1] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Lab Fisiol & Biol Mol, RA-1428 Buenos Aires, DF, Argentina
关键词
D O I
10.1016/j.ceb.2005.04.014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent findings justify a renewed interest in alternative splicing (AS): the process is more a rule than an exception as it affects the expression of 60% of human genes; it explains how a vast mammalian proteomic complexity is achieved with a limited number of genes; and mutations in AS regulatory sequences are a widespread source of human disease. AS regulation not only depends on the interaction of splicing factors with their target sequences in the pre-mRNA but is coupled to transcription. A clearer picture is emerging of the mechanisms by which transcription affects AS through promoter identity and occupation. These mechanisms involve the recruitment of factors with dual functions in transcription and splicing (i.e. that contain both functional domains and hence link the two processes) and the control of RNA polymerase II elongation.
引用
收藏
页码:262 / 268
页数:7
相关论文
共 47 条
[41]   SPECIFICITY OF RNA MATURATION PATHWAYS - RNAS TRANSCRIBED BY RNA POLYMERASE-III ARE NOT SUBSTRATES FOR SPLICING OR POLYADENYLATION [J].
SISODIA, SS ;
SOLLNERWEBB, B ;
CLEVELAND, DW .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (10) :3602-3612
[42]   TRANSCRIPTION OF HERPES-SIMPLEX VIRUS TK SEQUENCES UNDER THE CONTROL OF WILD-TYPE AND MUTANT HUMAN RNA POLYMERASE-I PROMOTERS [J].
SMALE, ST ;
TJIAN, R .
MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (02) :352-362
[43]   Chromatin modification by DNA tracking [J].
Travers, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) :13634-13637
[44]   Steroid hormones induce bcl-X gene expression through direct activation of distal promoter P4 [J].
Viegas, LR ;
Vicent, GP ;
Barañao, JL ;
Beato, M ;
Pecci, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (11) :9831-9839
[45]   Pin1 modulates the structure and function of human RNA polymerase II [J].
Xu, YX ;
Hirose, Y ;
Zhou, XZ ;
Lu, KP ;
Manley, JL .
GENES & DEVELOPMENT, 2003, 17 (22) :2765-2776
[46]   The C-terminal domain of the largest subunit of RNA polymerase II interacts with a novel set of serine/arginine-rich proteins [J].
Yuryev, A ;
Patturajan, M ;
Litingtung, Y ;
Joshi, RV ;
Gentile, C ;
Gebara, M ;
Corden, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) :6975-6980
[47]   Participation of the C-terminal domain of RNA polymerase II in exon definition during pre-mRNA splicing [J].
Zeng, CQ ;
Berget, SM .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (21) :8290-8301