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从重组亚基组装具有转录活性的RNA聚合酶I起始因子SL1。

Assembly of transcriptionally active RNA polymerase I initiation factor SL1 from recombinant subunits.

作者信息

Zomerdijk J C, Beckmann H, Comai L, Tjian R

机构信息

Howard Hughes Medical Institute, Department of Molecular and Cell Biology, University of California, Berkeley 94720-3204.

出版信息

Science. 1994 Dec 23;266(5193):2015-8. doi: 10.1126/science.7801130.

Abstract

Initiation of ribosomal RNA synthesis by RNA polymerase I requires the promoter selectivity factor SL1, which consists of the TATA-binding protein, TBP, and three associated factors, TAFIS 110, 63, and 48. Here the in vivo and in vitro assembly of functional SL1 complexes from recombinant TAFIS and TBP are reported. Complexes containing TBP and all three TAFIS were as active in supporting transcription from the human ribosomal RNA gene promoter as endogenous SL1, whereas partial complexes without TBP did not efficiently direct transcription in vitro. These results suggest that TAFIS 110, 63, and 48, together with TBP, are necessary and sufficient to reconstitute a transcriptionally active SL1 complex.

摘要

RNA聚合酶I引发核糖体RNA合成需要启动子选择性因子SL1,它由TATA结合蛋白TBP以及三个相关因子TAFIS 110、63和48组成。本文报道了从重组TAFIS和TBP体内和体外组装功能性SL1复合物的过程。含有TBP和所有三个TAFIS的复合物在支持从人类核糖体RNA基因启动子转录方面与内源性SL1一样活跃,而不含TBP的部分复合物在体外不能有效地指导转录。这些结果表明,TAFIS 110、63和48与TBP一起,对于重建转录活性SL1复合物是必要且充分的。

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