Beall B, Lutkenhaus J
Department of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical Center, Kansas City 66103.
J Bacteriol. 1989 Dec;171(12):6821-34. doi: 10.1128/jb.171.12.6821-6834.1989.
Located at 135 degrees on the Bacillus subtilis genetic map are several genes suspected to be involved in cell division and sporulation. Previously isolated mutations mapping at 135 degrees include the tms-12 mutation and mutations in the B. subtilis homologs of the Escherichia coli cell division genes ftsA and ftsZ. Previously, we cloned and sequenced the B. subtilis ftsA and ftsZ genes that are present on an 11-kilobase-pair EcoRI fragment and found that the gene products and organization of these two genes are conserved between the two bacterial species. We have since found that the mutation in the temperature-sensitive filamenting tms-12 mutant maps upstream of the ftsA gene on the same 11-kilobase-pair EcoRI fragment in a gene we designated dds. Sequence analysis of the dds gene and four other open reading frames upstream of ftsA revealed no significant homology to other known genes. It was found that the dds gene is not absolutely essential for viability since the dds gene could be insertionally inactivated. The dds null mutants grew slowly, were filamentous, and exhibited a reduced level of sporulation. Additionally, these mutants were extremely temperature sensitive and were unable to form colonies at 37 degrees C. Another insertion, which resulted in the elimination of 103 C-terminal residues, resulted in a temperature-sensitive phenotype less severe than that in the dds null mutant and similar to that in the known tms-12 mutant. The tms-12 mutation was cloned and sequenced, revealing a nonsense codon that was predicted to result in an amber fragment that was about 65% of the wild-type size (elimination of 93 C-terminal residues).
在枯草芽孢杆菌遗传图谱的135度位置上有几个被怀疑参与细胞分裂和芽孢形成的基因。之前分离出的位于135度位置的突变包括tms - 12突变以及大肠杆菌细胞分裂基因ftsA和ftsZ在枯草芽孢杆菌中的同源基因突变。此前,我们克隆并测序了位于一个11千碱基对的EcoRI片段上的枯草芽孢杆菌ftsA和ftsZ基因,发现这两个基因的基因产物和基因组织在这两种细菌之间是保守的。此后我们发现,温度敏感型丝状化tms - 12突变体中的突变位于ftsA基因上游,在同一个11千碱基对的EcoRI片段上的一个我们命名为dds的基因中。对dds基因以及ftsA上游的其他四个开放阅读框的序列分析表明,它们与其他已知基因没有明显的同源性。已发现dds基因对于生存力并非绝对必需,因为dds基因可以被插入失活。dds基因缺失突变体生长缓慢,呈丝状,并且芽孢形成水平降低。此外,这些突变体对温度极其敏感,在37℃时无法形成菌落。另一个插入导致103个C末端残基被消除,产生了一种温度敏感型表型,其严重程度低于dds基因缺失突变体,与已知的tms - 12突变体相似。tms - 12突变被克隆并测序,揭示出一个无义密码子,预计会导致一个约为野生型大小65%的琥珀片段(消除93个C末端残基)。