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流产起始仅在腺病毒2型主要晚期启动子的一组下游突变体中最弱的成员中增加。

Abortive initiation is increased only for the weakest members of a set of down mutants of the adenovirus 2 major late promoter.

作者信息

Jacob G A, Luse S W, Luse D S

机构信息

Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati College of Medicine, Ohio 45267-0524.

出版信息

J Biol Chem. 1991 Nov 25;266(33):22537-44.

PMID:1939271
Abstract

We have shown that accurate initiation of productive RNA synthesis in vitro at the adenovirus 2 major late promoter is accompanied by abortive initiation of very short transcripts (Luse, D. S., and Jacob, G. A. (1987) J. Biol. Chem. 262, 14990-14997). We made a set of sequence variants of this promoter, using every possible base at position -28 (in the TATA box) in the context of either the normal base (A) or a T at position +1 on the nontemplate strand. All changes from wild type reduced promoter strength. The two weakest promoters were 10- and 30-fold less active than wild type in productive RNA synthesis. We tested the possibility that the down mutations also caused an increase in the proportion of in vitro initiations which are abortive. This effect was seen only with the two weakest members of the promoter set. For these promoters, which share an A----C change at the -28 position of the TATA box, the ratio of abortive to productive initiations was 3-4-fold higher than for the other promoters. Interestingly, the sequence change at +1, although a down mutation, did not lead to an increase in abortive initiation.

摘要

我们已经表明,在腺病毒2型主要晚期启动子处体外高效RNA合成的准确起始伴随着极短转录本的流产起始(卢斯,D. S.,和雅各布,G. A.(1987年)《生物化学杂志》262卷,14990 - 14997页)。我们制备了该启动子的一组序列变体,在非模板链上第 +1 位为正常碱基(A)或T的情况下,在 -28 位(TATA 框中)使用了每一种可能的碱基。与野生型相比,所有变化均降低了启动子强度。在高效RNA合成中,两个最弱的启动子的活性比野生型分别低10倍和30倍。我们测试了向下突变是否也会导致体外流产起始比例增加的可能性。仅在启动子组中两个最弱的成员中观察到这种效应。对于这些在TATA框 -28 位共享A→C变化的启动子,流产起始与高效起始的比率比其他启动子高3至4倍。有趣的是,+1 位的序列变化虽然是向下突变,但并未导致流产起始增加。

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