Forward translocation is the natural pathway of RNA release at an intrinsic terminator

被引:89
作者
Santangelo, TJ [1 ]
Roberts, JW [1 ]
机构
[1] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
关键词
D O I
10.1016/S1097-2765(04)00154-6
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
Intrinsic terminators of bacterial RNA polymerase are small < ∼30 bp) sequences containing a dyad symmetry that encodes a hairpin in the RNA, followed immediately by a uridine-rich stretch of 5-9 nucleotides just before the site of RNA release. Formation of the RNA hairpin destabilizes the elongation complex, leading to transcript release. We test a model in which hairpin formation drives RNA polymerase and the melted DNA bubble downstream without transcript elongation, thus releasing the transcript from its enclosure within the enzyme as an RNA/DNA hybrid. We show that blocking downstream translocation of RNAP and preventing downstream DNA unwinding both inhibit transcript release. We argue that translocation of RNA polymerase is essential and that translocation of the bubble stimulates, but is not required, for RNA release; we conclude that forward translocation is the natural pathway of RNA release at an intrinsic terminator.
引用
收藏
页码:117 / 126
页数:10
相关论文
共 21 条
[1]   GENE STRUCTURE, ORGANIZATION, AND EXPRESSION IN ARCHAEBACTERIA [J].
BROWN, JW ;
DANIELS, CJ ;
REEVE, JN .
CRC CRITICAL REVIEWS IN MICROBIOLOGY, 1989, 16 (04) :287-338
[2]   SYNTHESIS AND CHARACTERIZATION OF DISULFIDE CROSS-LINKED OLIGONUCLEOTIDES [J].
FERENTZ, AE ;
KEATING, TA ;
VERDINE, GL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (20) :9006-9014
[3]  
FERENTZ AE, 1994, NUCL ACIDS MOL BIOL, P14
[4]   Structural basis of transcription:: An RNA polymerase II elongation complex at 3.3 Å resolution [J].
Gnatt, AL ;
Cramer, P ;
Fu, JH ;
Bushnell, DA ;
Kornberg, RD .
SCIENCE, 2001, 292 (5523) :1876-1882
[5]   USE OF MONO-Q HIGH-RESOLUTION ION-EXCHANGE CHROMATOGRAPHY TO OBTAIN HIGHLY PURE AND ACTIVE ESCHERICHIA-COLI RNA-POLYMERASE [J].
HAGER, DA ;
JIN, DJ ;
BURGESS, RR .
BIOCHEMISTRY, 1990, 29 (34) :7890-7894
[6]   Shortening of RNA:DNA hybrid in the elongation complex of RNA polymerase is a prerequisite for transcription termination [J].
Komissarova, N ;
Becker, J ;
Solter, S ;
Kireeva, M ;
Kashlev, M .
MOLECULAR CELL, 2002, 10 (05) :1151-1162
[7]   A structural model of transcription elongation [J].
Korzheva, N ;
Mustaev, A ;
Kozlov, M ;
Malhotra, A ;
Nikiforov, V ;
Goldfarb, A ;
Darst, SA .
SCIENCE, 2000, 289 (5479) :619-625
[8]   DETERMINATION OF INTRINSIC TRANSCRIPTION TERMINATION EFFICIENCY BY RNA-POLYMERASE ELONGATION RATE [J].
MCDOWELL, JC ;
ROBERTS, JW ;
JIN, DJ ;
GROSS, C .
SCIENCE, 1994, 266 (5186) :822-825
[9]   COUPLING BETWEEN TRANSCRIPTION TERMINATION AND RNA-POLYMERASE INCHWORMING [J].
NUDLER, E ;
KASHLEV, M ;
NIKIFOROV, V ;
GOLDFARB, A .
CELL, 1995, 81 (03) :351-357
[10]   E-coli transcription repair coupling factor (Mfd protein) rescues arrested complexes by promoting forward translocation [J].
Park, JS ;
Marr, MT ;
Roberts, JW .
CELL, 2002, 109 (06) :757-767