Formation of the 3′ end of histone mRNA:: Getting closer to the end

被引:143
作者
Dominski, Zbigniew
Marzluff, William F.
机构
[1] Univ N Carolina, Program Mol Biol & Biotechnol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
关键词
historic mRNA; 3 ' end processing; cleavage and polyadenylation; U7; snRNP; CPSF-73; symplekin;
D O I
10.1016/j.gene.2007.04.021
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Nearly all eukaryotic mRNAs end with a poly(A) tail that is added to their 3' end by the ubiquitous cleavage/polyadenylation machinery. The only known exceptions to this rule are metazoan replication-dependent histone mRNAs, which end with a highly conserved stem-loop structure. This distinct 3' end is generated by specialized 3' end processing machinery that cleaves histone pre-mRNAs 4-5 nucleotides downstream of the stem-loop and consists of the U7 small nuclear RNP (snRNP) and number of protein factors. Recently, the U7 snRNP has been shown to contain a unique Sin core that differs from that of the spliceosomal snRNPs, and an essential heat labile processing factor has been identified as symplekin. In addition, crosslinking studies have pinpointed CPSF-73 as the endonuclease, which catalyzes the cleavage reaction. Thus, many of the critical components of the 3' end processing machinery are now identified. Strikingly, this machinery is not as unique as initially thought but contains at least two factors involved in cleavage/polyadenylation, suggesting that the two mechanisms have a common evolutionary origin. The greatest challenge that ties ahead is to determine how all these factors interact with each other to form a catalytically competent processing complex capable of cleaving histone pre-mRNAs. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:373 / 390
页数:18
相关论文
共 182 条
[1]   The stem-loop binding protein (SLBP1) is present in coiled bodies of the Xenopus germinal vesicle [J].
Abbott, J ;
Marzluff, WF ;
Gall, JG .
MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (02) :487-499
[2]   Functional coupling of cleavage and polyadenylation with transcription of mRNA [J].
Adamson, TE ;
Shutt, DC ;
Price, DH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (37) :32262-32271
[3]   Cotranscriptional processing of Drosophila histone mRNAs [J].
Adamson, TE ;
Price, DH .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (12) :4046-4055
[4]   Phosphorylation of serine 2 within the RNA polymerase IIC-terminal domain couples transcription and 3′ end processing [J].
Ahn, SH ;
Kim, M ;
Buratowski, S .
MOLECULAR CELL, 2004, 13 (01) :67-76
[5]  
[Anonymous], THEORETICAL ISSUES E
[6]  
Aravind L, 1999, In Silico Biol, V1, P69
[7]   Toward an assembly line for U7 snRNPs -: Interactions of U7-specific Lsm proteins with PRMT5 and SMN complexes [J].
Azzouz, TN ;
Pillai, RS ;
Däpp, C ;
Chari, A ;
Meister, G ;
Kambach, C ;
Fischer, U ;
Schümperli, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (41) :34435-34440
[8]   U7 snRNP-specific Lsm11 protein:: dual binding contacts with the 100 kDa zinc finger processing factor (ZFP100) and a ZFP100-independent function in histone RNA 3′ end processing [J].
Azzouz, TN ;
Gruber, A ;
Schümperli, D .
NUCLEIC ACIDS RESEARCH, 2005, 33 (07) :2106-2117
[9]   Evolutionary conservation of the U7 small nuclear ribonucleoprotein in Drosophila melanogaster [J].
Azzouz, TN ;
Schümperli, D .
RNA, 2003, 9 (12) :1532-1541
[10]   Integrator, a multiprotein mediator of small nuclear RNA processing, associates with the C-terminal repeat of RNA polymerase II [J].
Baillat, D ;
Hakimi, MA ;
Näär, AM ;
Shilatifard, A ;
Cooch, N ;
Shiekhattar, R .
CELL, 2005, 123 (02) :265-276