The TRAP100 component of the TRAP/Mediator complex is essential in broad transcriptional events and development

被引:97
作者
Ito, M
Okano, HJ
Darnell, RB
Roeder, RG [1 ]
机构
[1] Rockefeller Univ, Biochem & Mol Biol Lab, New York, NY 10021 USA
[2] Rockefeller Univ, Mol Neurooncol Lab, New York, NY 10021 USA
关键词
embryonic lethality; RNA polymerase II; TRAP100-TRAP95-SUR2; submodule; TRAP220; TRAP/Mediator;
D O I
10.1093/emboj/cdf348
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
The multisubunit TRAP/Mediator complex is a mammalian counterpart of the yeast Mediator that shows diverse coactivation functions. Genetic ablation of the murine TRAP100 component of this complex has revealed that it is not essential for cell viability per se. However, null mutant mice die at an early developmental stage with severe malformations, and cultured TRAP100-deficient cells exhibit attenuated functions of a wide variety of transcriptional activators on ectopic reporters. The TRAP100-deficient TRAP/Mediator complex also lacks TRAP95 and TRAP150beta/SUR2, which together with TRAP100 may form a submodule, and contains a reduced amount of SRB10/CDK8. Nevertheless, the residual complex shows unaltered binding both to RNA polymerase II and, with the exception of the oncoprotein E1A, to various activators. These findings suggest that TRAP/Mediator is broadly involved in transcription and that a TRAP100-containing submodule plays a secondary role, beyond primary activator interactions and RNA polymerase recruitment by the TRAP complex, in magnifying effects of activators on the general transcriptional machinery.
引用
收藏
页码:3464 / 3475
页数:12
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