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切除一个P4样隐匿性原噬菌体可导致大肠杆菌中Alp蛋白酶的表达。

Excision of a P4-like cryptic prophage leads to Alp protease expression in Escherichia coli.

作者信息

Kirby J E, Trempy J E, Gottesman S

机构信息

Laboratory of Molecular Biology, National Cancer Institute, Bethesda, Maryland 20892.

出版信息

J Bacteriol. 1994 Apr;176(7):2068-81. doi: 10.1128/jb.176.7.2068-2081.1994.

Abstract

The Escherichia coli K-12 alpA gene product, when overproduced from a multicopy plasmid, leads to suppression of the capsule overproduction and UV sensitivity phenotypes of cells mutant for the Lon ATP-dependent protease. This suppression has previously been shown to correlate with increased in vivo activity of a previously unknown energy-dependent proteolytic activity capable of degrading Lon substrates, the Alp protease. We show in an accompanying paper that alpA, which has homology to a short open reading frame in bacteriophage P4, acts as a positive transcriptional regulator of slpA, a gene linked to alpA and necessary for suppression of lon mutants (J. E. Trempy, J. E. Kirby, and S. Gottesman, J. Bacteriol. 176:2061-2067). The sequence of slpA suggests that it encodes an integrase gene closely related to P4 int and that both alpA and slpA are part of a cryptic P4-like prophage. AlpA expression increases SlpA synthesis. Increased SlpA leads, in turn, to the excision and loss of the cryptic prophage. Excision is dependent on integration host factor as well as on SlpA. Prophage excision is necessary but not sufficient for full expression of the Alp protease. A second function (named AHA) allows full protease expression; this function can be provided by the kanamycin resistance element from Tn903 when the element is present on a multicopy plasmid. Excision and loss of the cryptic prophage apparently allow expression of the Alp protease by inactivating a small stable RNA (10Sa RNA) encoded by the ssrA gene. The precursor of this RNA has its 3' end within the cryptic prophage; the mature 3' end lies within the prophage attL site. Inactivation of ssrA by insertional mutagenesis is sufficient to allow expression of the suppressing Alp protease, even in the presence of the cryptic prophage. Therefore, 10Sa RNA acts as a negative regulator of protease synthesis or activity, and prophage excision must inactivate this inhibitory function of the RNA.

摘要

大肠杆菌K-12 alpA基因产物从多拷贝质粒过量表达时,可抑制Lon ATP依赖性蛋白酶突变细胞的荚膜过度产生和紫外线敏感性表型。此前已证明这种抑制作用与一种先前未知的、能够降解Lon底物的能量依赖性蛋白水解活性(Alp蛋白酶)的体内活性增加相关。我们在一篇随附论文中表明,与噬菌体P4中的一个短开放阅读框具有同源性的alpA,作为slpA的正转录调节因子发挥作用,slpA是一个与alpA连锁且对抑制lon突变体必不可少的基因(J. E. Trempy、J. E. Kirby和S. Gottesman,《细菌学杂志》176:2061 - 2067)。slpA的序列表明它编码一个与P4 int密切相关的整合酶基因,并且alpA和slpA都是一个隐匿性P4样原噬菌体的一部分。AlpA表达增加SlpA的合成。SlpA增加进而导致隐匿性原噬菌体的切除和丢失。切除依赖于整合宿主因子以及SlpA。原噬菌体切除对于Alp蛋白酶的完全表达是必要的,但并不充分。第二个功能(命名为AHA)允许蛋白酶完全表达;当来自Tn903的卡那霉素抗性元件存在于多拷贝质粒上时,这个功能可以由它提供。隐匿性原噬菌体的切除和丢失显然通过使由ssrA基因编码的一种小的稳定RNA(10Sa RNA)失活而允许Alp蛋白酶表达。这种RNA的前体在其3'端位于隐匿性原噬菌体内部;成熟的3'端位于原噬菌体attL位点内。通过插入诱变使ssrA失活足以允许抑制性Alp蛋白酶表达,即使在存在隐匿性原噬菌体的情况下也是如此。因此,10Sa RNA作为蛋白酶合成或活性的负调节因子发挥作用,并且原噬菌体切除必须使RNA的这种抑制功能失活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02c1/205313/1e51974980d7/jbacter00025-0277-a.jpg

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