Orndorff P E, Spears P A, Schauer D, Falkow S
J Bacteriol. 1985 Oct;164(1):321-30. doi: 10.1128/jb.164.1.321-330.1985.
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.
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。