Distal enhancer regulation by promoter derepression in topologically constrained DNA in vitro

被引:24
作者
Barton, MC
Madani, N
Emerson, BM
机构
[1] UNIV CINCINNATI,SCH MED,DEPT MOL GENET,CINCINNATI,OH 45267
[2] OREGON HLTH SCI UNIV,SCH MED,DEPT BIOCHEM & MOL BIOL,PORTLAND,OR 97201
[3] SALK INST BIOL STUDIES,REGULATORY BIOL LAB,LA JOLLA,CA 92037
关键词
beta-globin gene; in vitro transcription; DNA topology; GATA-1; derepression; enhancers;
D O I
10.1073/pnas.94.14.7257
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
Long-range promoter-enhancer interactions are a crucial regulatory feature of many eukaryotic genes yet little is known about the mechanisms involved. Using cloned chicken beta(A)-globin genes, either individually or within the natural chromosomal locus, enhancer-dependent transcription is achieved in vitro at a distance of 2 kb with developmentally staged erythroid extracts. This occurs by promoter derepression and is critically dependent upon DNA topology. In the presence of the enhancer, genes must exist in a supercoiled conformation to be actively transcribed, whereas relaxed or linear templates are inactive. Distal protein-protein interactions in vitro may be favored on supercoiled DNA because of topological constraints. In this system, enhancers act primarily to increase the probability of rapid and efficient transcription complex formation and initiation. Repressor and activator proteins binding within the promoter, including erythroid-specific GATA-1, mediate this process.
引用
收藏
页码:7257 / 7262
页数:6
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