Transcription termination by RNA polymerase III in fission yeast - A genetic and biochemically tractable model system

被引:64
作者
Hamada, M [1 ]
Sakulich, AL [1 ]
Koduru, SB [1 ]
Maraia, RJ [1 ]
机构
[1] NICHHD, Lab Mol Growth Regulat, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1074/jbc.M003980200
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
In order for RNA polymerase (pol) III to produce a sufficient quantity of RNAs of appropriate structure, initiation, termination, and reinitiation must be accurate and efficient. Termination-associated factors have been shown to facilitate reinitiation and regulate transcription in some species. Suppressor tRNA genes that differ in the dT(n) termination signal were examined for function in Schizosaccharomyces pombe, We also developed an S. pombe extract that is active for tRNA transcription that is described here for the first time. The ability of this tRNA gene to be transcribed in extracts from different species allowed us to compare termination in three model systems. Although human pol III terminates efficiently at 4 dTs and S. pombe at 5 dTs, Saccharomyces cerevisiae pol III requires 6 dTs to direct comparable but lower termination efficiency and also appears qualitatively distinct. Interestingly, this pattern of sensitivity to a minimal dT(n) termination signal was found to correlate with the sensitivity to alpha-amanitin, as S. pombe was intermediate between human and S. cerevisiae pols III. The results establish that the pols III of S. cerevisiae, S. pombe, and human exhibit distinctive properties and that termination occurs in S. pombe in a manner that is functionally more similar to human than is S. cerevisiae.
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收藏
页码:29076 / 29081
页数:6
相关论文
共 63 条
[1]   GENERATION OF LONG READ-THROUGH TRANSCRIPTS INVIVO AND INVITRO BY DELETION OF 3' TERMINATION AND PROCESSING SEQUENCES IN THE HUMAN TRANSFER RNAIMET GENE [J].
ADENIYIJONES, S ;
ROMEO, PH ;
ZASLOFF, M .
NUCLEIC ACIDS RESEARCH, 1984, 12 (02) :1101-1115
[2]   EFFECTS OF ALTERATIONS IN THE 3' FLANKING SEQUENCE ON INVIVO AND INVITRO EXPRESSION OF THE YEAST SUP4-0 TRANSFER RNATYR GENE [J].
ALLISON, DS ;
HALL, BD .
EMBO JOURNAL, 1985, 4 (10) :2657-2664
[3]  
Arrebola R, 1998, MOL CELL BIOL, V18, P1
[4]  
Baserga S., 1993, In The RNA world, P359
[5]   Substrate specificity of the RNase activity of yeast RNA polymerase III [J].
Bobkova, EV ;
Hall, BD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (36) :22832-22839
[6]   NUCLEOTIDE-SEQUENCES IN XENOPUS 5S DNA REQUIRED FOR TRANSCRIPTION TERMINATION [J].
BOGENHAGEN, DF ;
BROWN, DD .
CELL, 1981, 24 (01) :261-270
[7]   TRANSCRIPTION TERMINATION BY RNA POLYMERASE-III - UNCOUPLING OF POLYMERASE RELEASE FROM TERMINATION SIGNAL RECOGNITION [J].
CAMPBELL, FE ;
SETZER, DR .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (05) :2260-2272
[8]  
CASTANO JG, 1985, J BIOL CHEM, V260, P9002
[9]   ACTION OF ALPHA-AMANITIN DURING PYROPHOSPHOROLYSIS AND ELONGATION BY RNA-POLYMERASE-II [J].
CHAFIN, DR ;
GUO, HL ;
PRICE, DH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (32) :19114-19119
[10]   The RNA cleavage activity of RNA polymerase III is mediated by an essential TFIIS-like subunit and is important for transcription termination [J].
Chédin, S ;
Riva, M ;
Schultz, P ;
Sentenac, A ;
Carles, C .
GENES & DEVELOPMENT, 1998, 12 (24) :3857-3871