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大肠杆菌中编码1型菌毛蛋白的基因pilA的两种调控模式。

Two modes of control of pilA, the gene encoding type 1 pilin in Escherichia coli.

作者信息

Orndorff P E, Spears P A, Schauer D, Falkow S

出版信息

J Bacteriol. 1985 Oct;164(1):321-30. doi: 10.1128/jb.164.1.321-330.1985.

Abstract

Type 1 piliation in Escherichia coli is subject to metastable regulation at the transcriptional level (B. I. Eisenstein, Science 214:337-339, 1981). However, the genes controlling in this fashion are not known. We present evidence that the pilA gene, encoding the structural subunit of type 1 pili, is subject to metastable transcriptional regulation. A pilA'-lacZ fusion, constructed in vitro on a recombinant plasmid, was used in conjunction with a recBC sbcB mutant of E. coli K-12 to introduce the fusion into the chromosomal region encoding Pil. This fusion was found to be subject to metastable transcriptional control. The rate of switching from the Lac+ to the Lac- phenotype was 4 X 10(-4) per cell per generation and 6.2 X 10(-4) in the opposite direction. A ca. 10-fold difference in beta-galactosidase activity was observed between phenotypically "ON" (Lac+) and "OFF" (Lac-) populations. P1 transduction experiments showed that the element determining the ON or OFF phenotype was tightly linked to pilA. In addition to the metastable regulation of pilA, a second type of transcriptional regulation was effected by the product of a gene, hyp, adjacent to pilA. By using a recombinant plasmid containing just a pilA'-lacZ fusion and the putative pilA promoter, we found that a lesion in hyp conferred a beta-galactosidase activity about fivefold higher than that of a strain possessing the parental hyp gene. Mutants constructed to have a pilA'-lacZ fusion and a hyp::Tn5-132 mutation in the chromosome exhibited a frequency of switching from Lac+ to Lac- and vice versa indistinguishable from that of the parental strain. However, in the ON mode, hyp::Tn5-132 mutants showed a twofold-higher beta-galactosidase activity. Thus, hyp does not appear to affect metastable variation but does affect the level of transcription of the pilA gene in the ON (transcribed) mode.

摘要

大肠杆菌中的1型菌毛在转录水平上受到亚稳定调控(B. I. 艾森斯坦,《科学》214:337 - 339,1981)。然而,以这种方式控制的基因尚不清楚。我们提供证据表明,编码1型菌毛结构亚基的pilA基因受到亚稳定转录调控。在重组质粒上体外构建的pilA'-lacZ融合体与大肠杆菌K - 12的recBC sbcB突变体一起用于将融合体引入编码菌毛蛋白(Pil)的染色体区域。发现该融合体受到亚稳定转录控制。从Lac +表型转换为Lac -表型的速率为每细胞每代4×10⁻⁴,相反方向为6.2×10⁻⁴。在表型上“开启”(Lac +)和“关闭”(Lac -)的群体之间观察到β - 半乳糖苷酶活性约有10倍的差异。P1转导实验表明,决定开启或关闭表型的元件与pilA紧密连锁。除了pilA的亚稳定调控外,第二种转录调控类型由与pilA相邻的hyp基因的产物介导。通过使用仅包含pilA'-lacZ融合体和假定的pilA启动子的重组质粒,我们发现hyp中的损伤赋予的β - 半乳糖苷酶活性比具有亲本hyp基因的菌株高约五倍。构建的在染色体上具有pilA'-lacZ融合体和hyp::Tn5 - 132突变的突变体,从Lac +转换为Lac -以及反之亦然的频率与亲本菌株无明显差异。然而,在开启模式下,hyp::Tn5 - 132突变体显示出两倍高的β - 半乳糖苷酶活性。因此,hyp似乎不影响亚稳定变异,但确实影响pilA基因在开启(转录)模式下的转录水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28e0/214247/301aac443423/jbacter00215-0335-a.jpg

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