Alternative splicing of U12-type introns

被引:3
作者
Chang, Wen-Cheng [1 ,2 ]
Chen, Hung-Hsi [1 ]
Tarn, Woan-Yuh [1 ]
机构
[1] Acad Sinica, Inst Biomed Sci, Taipei 115, Taiwan
[2] Natl Def Med Ctr, Grad Inst Life Sci, Taipei, Taiwan
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2008年 / 13卷
关键词
alternative splicing; U2-type intron; U12-type intron; U2; spliceosome; hybrid intron; U12; splice site selection; exon skipping; intron retention; review;
D O I
10.2741/2791
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
Precise removal of introns from metazoan precursor mRNAs is critical for gene expression. Nevertheless, alternative splicing provides a means for higher eukaryotes to increase genomic complexity and proteome diversity and to regulate certain cellular functions. The presence of rare U12-type pre-mRNA introns in eukaryotic genomes further complicates splicing events. In this review, we discuss the mechanism of U12-type intron splicing with emphasis on how the U12 spliceosome selects alternative splice sites in various U12-type intron-containing pre-mRNAs. Moreover, we propose possible roles for U12-type introns in a wide range of gene regulation through splicing regulation.
引用
收藏
页码:1681 / 1690
页数:10
相关论文
共 99 条
[1]   U12DB: a database of orthologous U12-type spliceosomal introns [J].
Alioto, Tyler S. .
NUCLEIC ACIDS RESEARCH, 2007, 35 :D110-D115
[2]   NCAM1 association study of bipolar disorder and schizophrenia: polymorphisms and alternatively spliced isoforms lead to similarities and differences [J].
Atz, Mary E. ;
Rollins, Brandi ;
Vawter, Marquis P. .
PSYCHIATRIC GENETICS, 2007, 17 (02) :55-67
[3]   Sequence conservation, relative isoform frequencies, and nonsense-mediated decay in evolutionarily conserved alternative splicing [J].
Baek, D ;
Green, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (36) :12813-12818
[4]   Splicing in action: assessing disease causing sequence changes [J].
Baralle, D ;
Baralle, M .
JOURNAL OF MEDICAL GENETICS, 2005, 42 (10) :737-748
[5]   Donor splice-site mutations in WT1 are responsible for Frasier syndrome [J].
Barbaux, S ;
Niaudet, P ;
Gubler, MC ;
Grunfeld, JP ;
Jaubert, F ;
Kuttenn, F ;
Fekete, CN ;
SouleyreauTherville, N ;
Thibaud, E ;
Fellous, M ;
McElreavey, K .
NATURE GENETICS, 1997, 17 (04) :467-470
[6]  
Bartosova Z, 2007, NEOPLASMA, V54, P101
[7]   EXON RECOGNITION IN VERTEBRATE SPLICING [J].
BERGET, SM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (06) :2411-2414
[8]   Mechanisms of alternative pre-messenger RNA splicing [J].
Black, DL .
ANNUAL REVIEW OF BIOCHEMISTRY, 2003, 72 :291-336
[9]   Alternative splicing: New insights from global analyses [J].
Blencowe, Benjamin J. .
CELL, 2006, 126 (01) :37-47
[10]   The relevance of alternative RNA splicing to pharmacogenomics [J].
Bracco, L ;
Kearsey, J .
TRENDS IN BIOTECHNOLOGY, 2003, 21 (08) :346-353