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启动子活性的序列决定因素。

Sequence determinants of promoter activity.

作者信息

Youderian P, Bouvier S, Susskind M M

出版信息

Cell. 1982 Oct;30(3):843-53. doi: 10.1016/0092-8674(82)90289-6.

Abstract

The bacteriophage P22 promoter for the antirepressor (ant) gene, Pant, in the absence of Arc repressor, directs the synthesis of extremely high levels of antirepressor. Overproduction of antirepressor leads secondarily to the failure to produce progeny phage upon lytic infection. A substantial fraction of revertants of P22 arc-amber phage are pseudorevertants that have acquired additional mutations that decrease the activity of the ant promoter. DNA sequence analysis of 72 independent Pant "promoter-down" mutations reveals more than 25 different alterations that define two regions critical for promoter activity. With few exceptions, these promoter-down mutations decrease the homology of Pant with the consensus promoter sequence, demonstrating that the conserved features among a large number of different wild-type promoters are the determinants of promoter strength.l In general, different substitution mutations at the same site within the promoter have similar effects, resulting in either a severe or a mild reduction in promoter activity.

摘要

在没有Arc阻遏物的情况下,抗阻遏物(ant)基因的噬菌体P22启动子Pant可指导合成极高水平的抗阻遏物。抗阻遏物的过量产生继而导致溶菌感染时无法产生子代噬菌体。P22 arc-琥珀突变噬菌体的很大一部分回复突变体是假回复突变体,它们获得了额外的突变,从而降低了ant启动子的活性。对72个独立的Pant“启动子下调”突变进行的DNA序列分析揭示了25种以上不同的改变,这些改变定义了对启动子活性至关重要的两个区域。除了少数例外,这些启动子下调突变降低了Pant与共有启动子序列的同源性,表明大量不同野生型启动子中的保守特征是启动子强度的决定因素。一般来说,启动子内同一位点的不同取代突变具有相似的效果,导致启动子活性严重或轻度降低。

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