Bioinformatic identification of candidate cis-regulatory elements involved in human mRNA polyadenylation

被引:197
作者
Hu, J
Lutz, CS
Wilusz, J
Tian, B [1 ]
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Biochem & Mol Biol, Newark, NJ 07101 USA
[2] Colorado State Univ, Dept Microbiol Immunol & Pathol, Ft Collins, CO 80523 USA
关键词
polyadenylation; cis elements; regulation;
D O I
10.1261/rna.2107305
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
Polyadenylation is an essential step for the maturation of almost all cellular mRNAs in eukaryotes. in human cells, most poly(A) sites are flanked by the upstream AAUAAA hexamer or a close variant, and downstream U/GU-rich elements. In yeast and plants, additional cis elements have been found to be located upstream of the poly(A) site, including UGUA, UAUA, and U-rich elements. In this study, we have developed a computer program named PROBE (Polyadenylation-Related Oligonucleotide Bidimensional Enrichment) to identify cis elements that may play regulatory roles in mRNA polyadenylation. By comparing human genomic sequences surrounding frequently used poly(A) sites with those surrounding less frequently used ones, we found that cis elements occurring in yeast and plants also exist in human poly(A) regions, including the upstream U-rich elements, and UAUA and UGUA elements. In addition, several novel elements were found to be associated with human poly(A) sites, including several G-rich elements. Thus, we suggest that many cis elements are evolutionarily conserved among eukaryotes, and human poly(A) sites have an additional set of cis elements that may be involved in the regulation of mRNA polyadenylation.
引用
收藏
页码:1485 / 1493
页数:9
相关论文
共 42 条
[1]   Downstream sequence elements with different affinities for the hnRNP H/H′ protein influence the processing efficiency of mammalian polyadenylation signals [J].
Arhin, GK ;
Boots, M ;
Bagga, PS ;
Milcarek, C ;
Wilusz, J .
NUCLEIC ACIDS RESEARCH, 2002, 30 (08) :1842-1850
[2]   THE G-RICH AUXILIARY DOWNSTREAM ELEMENT HAS DISTINCT SEQUENCE AND POSITION REQUIREMENTS AND MEDIATES EFFICIENT 3' END PRE-MESSENGER-RNA PROCESSING THROUGH A TRANS-ACTING FACTOR [J].
BAGGA, PS ;
FORD, LP ;
CHEN, F ;
WILUSZ, J .
NUCLEIC ACIDS RESEARCH, 1995, 23 (09) :1625-1631
[3]   ARED: human AU-rich element-containing mRNA database reveals an unexpectedly diverse functional repertoire of encoded proteins [J].
Bakheet, T ;
Frevel, M ;
Williams, BRG ;
Greer, W ;
Khabar, KSA .
NUCLEIC ACIDS RESEARCH, 2001, 29 (01) :246-254
[4]   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
[5]   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
[6]   Recognition of GU-rich polyadenylation regulatory elements by human CstF-64 protein [J].
Cañadillas, JMP ;
Varani, G .
EMBO JOURNAL, 2003, 22 (11) :2821-2830
[7]   EFFICIENCY OF UTILIZATION OF THE SIMIAN VIRUS-40 LATE POLYADENYLATION SITE - EFFECTS OF UPSTREAM SEQUENCES [J].
CARSWELL, S ;
ALWINE, JC .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (10) :4248-4258
[8]   AU-RICH ELEMENTS - CHARACTERIZATION AND IMPORTANCE IN MESSENGER-RNA DEGRADATION [J].
CHEN, CYA ;
SHYU, AB .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (11) :465-470
[9]   CLEAVAGE SITE DETERMINANTS IN THE MAMMALIAN POLYADENYLATION SIGNAL [J].
CHEN, F ;
MACDONALD, CC ;
WILUSZ, J .
NUCLEIC ACIDS RESEARCH, 1995, 23 (14) :2614-2620
[10]   SEQUENCE AND POSITION REQUIREMENTS FOR URIDYLATE-RICH DOWNSTREAM ELEMENTS OF POLYADENYLATION SIGNALS [J].
CHOU, ZF ;
CHEN, F ;
WILUSZ, J .
NUCLEIC ACIDS RESEARCH, 1994, 22 (13) :2525-2531