Guo D, Wu Y, Kaplan H B
Department of Microbiology and Molecular Genetics, The University of Texas-Houston Medical School, Houston, Texas 77030, USA.
J Bacteriol. 2000 Aug;182(16):4564-71. doi: 10.1128/JB.182.16.4564-4571.2000.
Starvation and cell density regulate the developmental expression of Myxococcus xanthus gene 4521. Three classes of mutants allow expression of this developmental gene during growth on nutrient agar, such that colonies of strains containing a Tn5 lac Omega4521 fusion are Lac(+). One class of these mutants inactivates SasN, a negative regulator of 4521 expression; another class activates SasS, a sensor kinase-positive regulator of 4521 expression; and a third class blocks lipopolysaccharide (LPS) O-antigen biosynthesis. To identify additional positive regulators of 4521 expression, 11 Lac(-) TnV. AS transposon insertion mutants were isolated from a screen of 18,000 Lac(+) LPS O-antigen mutants containing Tn5 lac Omega4521 (Tc(r)). Ten mutations identified genes that could encode positive regulators of 4521 developmental expression based on their ability to abolish 4521 expression during development in the absence of LPS O antigen and in an otherwise wild-type background. Eight of these mutations mapped to the sasB locus, which encodes the known 4521 regulators SasS and SasN. One mapped to sasS, whereas seven identified new genes. Three mutations mapped to a gene encoding an NtrC-like response regulator homologue, designated sasR, and four others mapped to a gene designated sasP. One mutation, designated ssp10, specifically suppressed the LPS O-antigen defect; the ssp10 mutation had no effect on 4521 expression in an otherwise wild-type background but reduced 4521 developmental expression in the absence of LPS O antigen to a level close to that of the parent strain. All of the mutations except those in sasP conferred defects during growth and development. These data indicate that a number of elements are required for 4521 developmental expression and that most of these are necessary for normal growth and fruiting body development.
饥饿和细胞密度调节黄色黏球菌基因4521的发育表达。三类突变体可使该发育基因在营养琼脂上生长期间表达,从而使含有Tn5 lac Omega4521融合体的菌株菌落呈Lac(+)。其中一类突变体使SasN失活,SasN是4521表达的负调节因子;另一类激活SasS,SasS是4521表达的传感激酶阳性调节因子;第三类阻断脂多糖(LPS)O抗原生物合成。为了鉴定4521表达的其他正调节因子,从18000个含有Tn5 lac Omega4521(Tc(r))的Lac(+) LPS O抗原突变体筛选中分离出11个Lac(-) TnV. AS转座子插入突变体。基于在没有LPS O抗原且在其他方面为野生型背景下发育期间消除4521表达的能力,10个突变鉴定出可能编码4521发育表达正调节因子的基因。这些突变中的8个定位于sasB位点,该位点编码已知的4521调节因子SasS和SasN。一个定位于sasS,而7个鉴定出了新基因。3个突变定位于编码NtrC样应答调节因子同源物的基因,命名为sasR,另外4个定位于命名为sasP的基因。一个命名为ssp10的突变特异性抑制LPS O抗原缺陷;ssp10突变在其他方面为野生型背景下对4521表达没有影响,但在没有LPS O抗原的情况下将4521发育表达降低到接近亲本菌株的水平。除了sasP中的突变外,所有突变在生长和发育期间都导致缺陷。这些数据表明4个521发育表达需要许多元件,并且其中大多数对于正常生长和子实体发育是必需的。