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

机译:pilA的两种控制模式,即编码大肠杆菌中1型菌毛蛋白的基因。

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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.
机译:大肠杆菌中的1型毛发在转录水平上受到亚稳态调控(B. I. Eisenstein,Science 214:337-339,1981)。但是,以这种方式控制的基因尚不清楚。我们目前的证据,编码1型菌毛的结构亚基的pilA基因受到亚稳态转录调控。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突变体结合使用,以将融合体引入编码Pil的染色体区域。发现这种融合受到亚稳态转录控制。从Lac +切换到Lac-表型的速率为每代细胞每细胞4 X 10(-4),反方向为6.2 X 10(-4)。大约在表型上“ ON”(Lac +)和“ OFF”(Lac-)群体之间观察到β-半乳糖苷酶活性有10倍的差异。 P1转导实验表明,决定ON或OFF表型的元件与pilA紧密相关。除了对pilA的亚稳态调控外,第二种转录调控还受到与pilA相邻的hyp基因产物的影响。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中的病变所赋予的β-半乳糖苷酶活性比具有亲本hyp基因的菌株高约5倍。构建为在染色体中具有pilA'-lacZ融合体和hyp :: Tn5-132突变的突变体显示出从Lac +切换到Lac-的频率,反之亦然,与亲本菌株的频率没有区别。但是,在ON模式下,hyp :: Tn5-132突变体显示出更高的β-半乳糖苷酶活性。因此,hyp似乎不会影响亚稳态变异,但会影响ON(转录)模式下pilA基因的转录水平。

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