An intronic polyadenylation site in human and mouse CstF-77 genes suggests an evolutionarily conserved regulatory mechanism

被引:34
作者
Pan, ZH [1 ]
Zhang, HB [1 ]
Hague, LK [1 ]
Lee, JY [1 ]
Lutz, CS [1 ]
Tian, B [1 ]
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Biochem & Mol Biol, Newark, NJ 07101 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
polyadenylation; gene regulation; CstF-77; SAGE;
D O I
10.1016/j.gene.2005.09.024
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Human CstF-77 is one of the three subunits of cleavage stimulation factor (CstF) that is essential for mRNA polyadenylation. Its Drosophila homologue, suppressor of forked [su(f)], contains in intronic poly(A) site, which can lead to a short transcript without a stop codon. By both bioinformatic searches and validation with molecular biology experiments, we found that human and mouse CstF-77 genes also contain an intronic poly(A) site, which can be utilized to produce short CstF-77 transcripts lacking sequences encoding domains that are involved in many of the CstF-77 functions. The genomic sequence surrounding the poly(A) site is highly conserved among all vertebrates, but is not present in nonvertebrate species. Using public Serial Analysis of Gene Expression (SAGE) data, we found that the intronic poly(A) site is utilized in a wide range of tissues. This finding indicates that vertebrates may employ a similar alternative polyadenylation mechanism to modulate CstF-77, highlighting the importance of the regulation of CstF-77 in various species. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:325 / 334
页数:10
相关论文
共 48 条
[1]   Whole-genome shotgun assembly and analysis of the genome of Fugu rubripes [J].
Aparicio, S ;
Chapman, J ;
Stupka, E ;
Putnam, N ;
Chia, J ;
Dehal, P ;
Christoffels, A ;
Rash, S ;
Hoon, S ;
Smit, A ;
Gelpke, MDS ;
Roach, J ;
Oh, T ;
Ho, IY ;
Wong, M ;
Detter, C ;
Verhoef, F ;
Predki, P ;
Tay, A ;
Lucas, S ;
Richardson, P ;
Smith, SF ;
Clark, MS ;
Edwards, YJK ;
Doggett, N ;
Zharkikh, A ;
Tavtigian, SV ;
Pruss, D ;
Barnstead, M ;
Evans, C ;
Baden, H ;
Powell, J ;
Glusman, G ;
Rowen, L ;
Hood, L ;
Tan, YH ;
Elgar, G ;
Hawkins, T ;
Venkatesh, B ;
Rokhsar, D ;
Brenner, S .
SCIENCE, 2002, 297 (5585) :1301-1310
[2]   Autoregulation at the level of mRNA 3′ end formation of the suppressor of forked gene of Drosophila melanogaster is conserved in Drosophila virilis [J].
Audibert, A ;
Simonelig, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (24) :14302-14307
[3]  
Barrett T, 2005, NUCLEIC ACIDS RES, V33, pD562
[4]  
Bateman A, 2004, NUCLEIC ACIDS RES, V32, pD138, DOI [10.1093/nar/gkp985, 10.1093/nar/gkr1065, 10.1093/nar/gkh121]
[5]   Patterns of variant polyadenylation signal usage in human genes [J].
Beaudoing, E ;
Freier, S ;
Wyatt, JR ;
Claverie, JM ;
Gautheret, D .
GENOME RESEARCH, 2000, 10 (07) :1001-1010
[6]   Chimeric human CstF-77/Drosophila suppressor of forked proteins rescue suppressor of forked mutant lethality and mRNA 3′ end processing in Drosophila [J].
Benoit, B ;
Juge, F ;
Iral, F ;
Audibert, A ;
Simonelig, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10593-10598
[7]   Poly(A) tail length control in Saccharomyces cerevisiae occurs by message-specific deadenylation [J].
Brown, CE ;
Sachs, AB .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (11) :6548-6559
[8]   EFFICIENT POLYADENYLATION WITHIN THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 LONG TERMINAL REPEAT REQUIRES FLANKING U3-SPECIFIC SEQUENCES [J].
BROWN, PH ;
TILEY, LS ;
CULLEN, BR .
JOURNAL OF VIROLOGY, 1991, 65 (06) :3340-3343
[9]   B-cell and plasma-cell splicing differences: A potential role in regulated immunoglobulin RNA processing [J].
Bruce, SR ;
Dingle, RWC ;
Peterson, ML .
RNA, 2003, 9 (10) :1264-1273
[10]   Recognition of GU-rich polyadenylation regulatory elements by human CstF-64 protein [J].
Cañadillas, JMP ;
Varani, G .
EMBO JOURNAL, 2003, 22 (11) :2821-2830