THE ELONGATION-TERMINATION DECISION IN TRANSCRIPTION

被引:84
作者
VONHIPPEL, PH [1 ]
YAGER, TD [1 ]
机构
[1] UNIV OREGON,DEPT CHEM,EUGENE,OR 97403
关键词
D O I
10.1126/science.1536005
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
At any template position, the decision to extend the transcript by one residue or to release the nascent RNA represents a kinetic competition between elongation and termination pathways. This competition is discussed in terms of alternative Eyring transition state barriers; changes in termination efficiency correspond to small changes in the relative heights of these barriers. Elongation complexes are stable at nonterminator positions; a model is presented to explain the destabilization of these complexes at intrinsic termination sites. Functionally analogous effects can operate at rho-dependent terminators. Mechanisms for modulation of termination efficiency by regulatory proteins are described.
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页码:809 / 812
页数:4
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