3′-End processing of pre-mRNA in eukaryotes

被引:194
作者
Wahle, E
Rüegsegger, U
机构
[1] Univ Halle Wittenberg, Inst Biochem, D-06120 Halle, Germany
[2] Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
关键词
RNA processing; poly(A) tail; polyadenylation;
D O I
10.1016/S0168-6445(99)00008-X
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
3'-Ends of almost all eukaryotic mRNAs are generated by endonucleolytic cleavage and addition of a poly(A) tail. In mammalian cells, the reaction depends on the sequence AAUAAA upstream of the cleavage site, a degenerate GU-rich sequence element downstream of the cleavage site and stimulatory sequences upstream of AAUAAA, Six factors have been identified that carry out the two reactions, With a single exception, they have been purified to homogeneity and cDNAs for 11 subunits have been cloned. Some of the cooperative RNA-protein and protein-protein interactions within the processing complex have been analyzed, but many details, including the identity of the endonuclease, remain unknown. Several examples of regulated polyadenylation are being analyzed at the molecular level. In the yeast Saccharomyces cerevisiae, sequences directing cleavage and polyadenylation are more degenerate than in metazoans, and a downstream element has not been identified. The list of processing factors may be complete now with approximately a dozen polypeptides, but their functions in the reaction are largely unknown. 3'-Processing is known to be coupled to transcription. This connection is thought to involve interactions of processing factors with the mRNA cap as well as with RNA polymerase II. (C) 1999 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:277 / 295
页数:19
相关论文
共 138 条
[1]   PCF11 encodes a third protein component of yeast cleavage and polyadenylation factor I [J].
Amrani, N ;
Minet, M ;
Wyers, F ;
Dufour, ME ;
Aggerbeck, LP ;
Lacroute, F .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (03) :1102-1109
[2]   Yeast Pab1 interacts with Rna15 and participates in the control of the poly(A) tail length in vitro [J].
Amrani, N ;
Minet, M ;
LeGouar, M ;
Lacroute, F ;
Wyers, F .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (07) :3694-3701
[3]   The suppressor of forked protein of Drosophila, a homologue of the human 77K protein required for mRNA 3′-end formation, accumulates in mitotically-active cells [J].
Audibert, A ;
Juge, F ;
Simonelig, M .
MECHANISMS OF DEVELOPMENT, 1998, 72 (1-2) :53-63
[4]   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
[5]   Solution structure of the N-terminal RNP domain of U1A protein: The role of C-terminal residues in structure stability and RNA binding [J].
Avis, JM ;
Allain, FHT ;
Howe, PWA ;
Varani, G ;
Nagai, K ;
Neuhaus, D .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 257 (02) :398-411
[6]  
Bai CY, 1996, MOL CELL BIOL, V16, P6661
[7]   Drosophila clipper/CPSF 30K is a post-transcriptionally regulated nuclear protein that binds RNA containing GC clusters [J].
Bai, CY ;
Tolias, PP .
NUCLEIC ACIDS RESEARCH, 1998, 26 (07) :1597-1604
[8]  
BALLANTYNE S, 1995, RNA, V1, P64
[9]   The 30-kD subunit of mammalian cleavage and polyadenylation specificity factor and its yeast homolog are RNA-binding zinc finger proteins [J].
Barabino, SML ;
Hubner, W ;
Jenny, A ;
MinvielleSebastia, L ;
Keller, W .
GENES & DEVELOPMENT, 1997, 11 (13) :1703-1716
[10]   DEGRADATION OF MESSENGER-RNA IN EUKARYOTES [J].
BEELMAN, CA ;
PARKER, R .
CELL, 1995, 81 (02) :179-183