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在非洲爪蟾中,稳定的聚合酶I启动子复合物的形成需要xUBF和Rib 1两者。

xUBF and Rib 1 are both required for formation of a stable polymerase I promoter complex in X. laevis.

作者信息

McStay B, Hu C H, Pikaard C S, Reeder R H

机构信息

Hutchinson Cancer Research Center, Basic Sciences Division, Seattle, WA 98104.

出版信息

EMBO J. 1991 Aug;10(8):2297-303. doi: 10.1002/j.1460-2075.1991.tb07766.x.

Abstract

We show that three protein fractions are required for accurate transcription initiation at a Xenopus laevis ribosomal gene promoter in vitro: RNA polymerase I, Rib1 and xUBF. The Rib1 and xUBF fractions are both necessary and sufficient for formation of a stable initiation complex. The xUBF fraction can be completely replaced by recombinant xUBF. We also report the sequence of a cDNA clone for xUBF. xUBF is 701 amino acids in length, contains domain which are related to a domain found in chromosomal proteins HMG 1 and 2, and has an acidic carboxy terminus of 87 amino acids. xUBF is closely similar in amino acid sequence to its previously reported human homolog, hUBF, except that xUBF has only three of the HMG-related domains while hUBF has four and therefore is 63 amino acids longer than xUBF.

摘要

我们发现,在非洲爪蟾核糖体基因启动子的体外精确转录起始过程中,需要三种蛋白质组分:RNA聚合酶I、Rib1和xUBF。Rib1和xUBF组分对于稳定起始复合物的形成既是必需的也是充分的。xUBF组分可以被重组xUBF完全替代。我们还报道了xUBF的cDNA克隆序列。xUBF长度为701个氨基酸,包含与染色体蛋白HMG 1和2中发现的一个结构域相关的结构域,并且有一个87个氨基酸的酸性羧基末端。xUBF的氨基酸序列与其先前报道的人类同源物hUBF非常相似,不同之处在于xUBF只有三个与HMG相关的结构域,而hUBF有四个,因此比xUBF长63个氨基酸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0803/452920/e09005d5a039/emboj00106-0327-a.jpg

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