snRNA 3′ end formation: the dawn of the Integrator complex

被引:59
作者
Chen, Jiandong
Wagner, Eric J. [1 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Dept Biochem & Mol Biol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
cleavage and polyadenylation specificity factor (CPSF); Integrator complex; beta-lactamase; RNA cleavage; RNA polymerase II; small nuclear RNA (snRNA); RNA-POLYMERASE-II; HISTONE MESSENGER-RNAS; POLYADENYLATION FACTOR CPSF-73; HUMAN U2 SNRNA; SMALL NUCLEAR; 3'-END FORMATION; BINDING-PROTEIN; U1; SNRNA; ELONGATION COMPLEX; GENE-EXPRESSION;
D O I
10.1042/BST0381082
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The ubiquitously expressed uridine-rich snRNAs (small nuclear RNAs) are essential for the removal of introns, proper expression of histone mRNA and biosynthesis of ribosomal RNA. Much is known about their assembly into snRNP (small nuclear ribonucleoprotein) particles and their ultimate function in the expression of other genes; however, in comparison, less is known about the biosynthesis of these critical non-coding RNAs. The sequence elements necessary for 3' end formation of snRNAs have been identified and, intriguingly, the processing of snRNAs is uniquely dependent on the snRNA promoter, indicating that co-transcriptional processing is important. However, the trans-acting RNA-processing factors that mediate snRNA processing remained elusive, hindering overall progress. Recently, the factors involved in this process were biochemically purified, and designated the Integrator complex. Since their initial discovery, Integrator proteins have been implicated not only in the production of snRNA, but also in other cellular processes that may be independent of snRNA biogenesis. In the present study, we discuss snRNA biosynthesis and the roles of Integrator proteins. We compare models of 3' end formation for different classes of RNA polymerase II transcripts and formulate/propose a model of Integrator function in snRNA biogenesis.
引用
收藏
页码:1082 / 1087
页数:6
相关论文
共 50 条
[1]
THE HIGHLY CONSERVED U SMALL NUCLEAR-RNA 3'-END FORMATION SIGNAL IS QUITE TOLERANT TO MUTATION [J].
ACH, RA ;
WEINER, AM .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (06) :2070-2079
[2]
TFIIH Kinase Places Bivalent Marks on the Carboxy-Terminal Domain of RNA Polymerase II [J].
Akhtar, Md. Sohail ;
Heidemann, Martin ;
Tietjen, Joshua R. ;
Zhang, David W. ;
Chapman, Rob D. ;
Eick, Dirk ;
Ansari, Aseem Z. .
MOLECULAR CELL, 2009, 34 (03) :387-393
[3]
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
[4]
Progression through the RNA Polymerase II CTD Cycle [J].
Buratowski, Stephen .
MOLECULAR CELL, 2009, 36 (04) :541-546
[5]
Metallo-β-lactamase fold within nucleic acids processing enzymes:: the β-CASP family [J].
Callebaut, I ;
Moshous, D ;
Mornon, JP ;
de Villartay, JP .
NUCLEIC ACIDS RESEARCH, 2002, 30 (16) :3592-3601
[6]
A COMMON OCTAMER MOTIF BINDING-PROTEIN IS INVOLVED IN THE TRANSCRIPTION OF U6 SNRNA BY RNA POLYMERASE-III AND U2 SNRNA BY RNA POLYMERASE-II [J].
CARBON, P ;
MURGO, S ;
EBEL, JP ;
KROL, A ;
TEBB, G ;
MATTAJ, IW .
CELL, 1987, 51 (01) :71-79
[7]
SEA-URCHIN SMALL NUCLEAR-RNA GENES ARE ORGANIZED IN DISTINCT TANDEMLY REPEATING UNITS [J].
CARD, CO ;
MORRIS, GF ;
BROWN, DT ;
MARZLUFF, WF .
NUCLEIC ACIDS RESEARCH, 1982, 10 (23) :7677-7688
[8]
Transcribing RNA polymerase II is phosphorylated at CTD residue serine-7 [J].
Chapman, Rob D. ;
Heidemann, Martin ;
Albert, Thomas K. ;
Mailhammer, Reinhard ;
Flatley, Andrew ;
Meisterernst, Michael ;
Kremmer, Elisabeth ;
Eick, Dirk .
SCIENCE, 2007, 318 (5857) :1780-1782
[9]
Transcription of the human U2 snRNA genes continues beyond the 3′ box in vivo [J].
Cuello, P ;
Boyd, DC ;
Dye, MJ ;
Proudfoot, NJ ;
Murphy, S .
EMBO JOURNAL, 1999, 18 (10) :2867-2877
[10]
DEVEGVAR HEN, 1986, CELL, V47, P259