Overlapping promoter targeting by Elk-1 and other divergent ETS-domain transcription factor family members

被引:33
作者
Boros, Joanna [1 ]
O'Donnell, Amanda [1 ]
Donaldson, Ian J. [1 ]
Kasza, Aneta [1 ]
Zeef, Leo [1 ]
Sharrocks, Andrew D. [1 ]
机构
[1] Univ Manchester, Fac Life Sci, Manchester M13 9PT, Lancs, England
基金
英国惠康基金;
关键词
SERUM RESPONSE FACTOR; TERNARY COMPLEX FACTORS; FACTOR-BINDING SITES; EXPRESSION; PROTEIN; GENE; SPECIFICITY; INHIBITION; SAP-1; WEB;
D O I
10.1093/nar/gkp804
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
ETS-domain transcription factors play important roles in controlling gene expression in a variety of different contexts; however, these proteins bind to very similar sites and it is unclear how in vivo specificity is achieved. In silico analysis is unlikely to reveal specific targets for individual family members and direct experimental approaches are therefore required. Here, we take advantage of an inducible dominant-negative expression system to identify a group of novel target genes for the ETS-domain transcription factor Elk-1. Elk-1 is thought to mainly function through cooperation with a second transcription factor SRF, but the targets we identify are largely SRF-independent. Furthermore, we demonstrate that there is a high degree of overlapping, cell type-specific, target gene binding by Elk-1 and other ETS-domain transcription factors. Our results are therefore consistent with the notion that there is a high degree of functional redundancy in target gene regulation by ETS-domain transcription factors in addition to the specific target gene regulation that can be dictated through heterotypic interactions exemplified by the Elk-1-SRF complex.
引用
收藏
页码:7368 / 7380
页数:13
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