Apelian D, Inouye S
Department of Biochemistry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway 08854-5635.
J Bacteriol. 1993 Jun;175(11):3335-42. doi: 10.1128/jb.175.11.3335-3342.1993.
A third putative sigma factor gene, sigC, has been isolated from Myxococcus xanthus by using the sigA gene (formerly rpoD of M. xanthus) as a probe. The nucleotide sequence of sigC has been determined, and an open reading frame of 295 residues (M(r) = 33,430) has been identified. The deduced amino acid sequence of sigC exhibits the features which are characteristic of other bacterial sigma factors. The characterization of a sigC-lacZ strain has demonstrated that sigC expression is induced immediately after cells enter into the developmental cycle and is dramatically reduced at the onset of sporulation. A deletion mutant of sigC grows normally in vegetative culture and is able to develop normally. However, in contrast to the wild-type cells, the sigC deletion mutant cells became capable of forming fruiting bodies and myxospores on semirich agar plates. This suggests that sigC may play a role in expression of genes involved in negatively regulating the initiation of fruiting body formation.
通过使用sigA基因(以前称为黄色粘球菌的rpoD)作为探针,从黄色粘球菌中分离出了第三个假定的σ因子基因sigC。已确定sigC的核苷酸序列,并鉴定出一个由295个残基组成的开放阅读框(M(r)=33430)。sigC推导的氨基酸序列具有其他细菌σ因子的特征。对sigC-lacZ菌株的表征表明,sigC表达在细胞进入发育周期后立即被诱导,并在孢子形成开始时显著降低。sigC的缺失突变体在营养培养中正常生长,并且能够正常发育。然而,与野生型细胞相比,sigC缺失突变体细胞能够在半丰富琼脂平板上形成子实体和粘孢子。这表明sigC可能在参与负调控子实体形成起始的基因表达中起作用。