Podbielski A, Woischnik M, Leonard B A, Schmidt K H
Department of Medical Microbiology and Hygiene, University Hospital Ulm, Germany.
Mol Microbiol. 1999 Feb;31(4):1051-64. doi: 10.1046/j.1365-2958.1999.01241.x.
During sequencing of an 11.5 kb genomic region of a serotype M49 group A streptococcal (GAS) strain, a series of genes were identified including nra(negative regulator of GAS). Transcriptional analysis of the region revealed that nra was primarily monocistronically transcribed. Polycistronic expression was found for the three open reading frames (ORFs) downstream and for the four ORFs upstream of nra. The deduced Nra protein sequence exhibited 62% homology to the GAS RofA positive regulator. In contrast to RofA, Nra was found to be a negative regulator of its own expression and that of the two adjacent operons by analysis of insertional inactivation mutants. By polymerase chain reaction and hybridization assays of 10 different GAS serotypes, the genomic presence of nra, rofA or both was demonstrated. Nra-regulated genes include the fibronectin-binding protein F2 gene (prtF2) and a novel collagen-binding protein (cpa). The Cpa polypeptide was purified as a recombinant maltose-binding protein fusion and shown to bind type I collagen but not fibronectin. In accordance with nra acting as a negative regulator of prtF2 and cpa, levels of attachment of the nra mutant strain to immobilized collagen and fibronectin was increased above wild-type levels. In addition, nra was also found to regulate negatively (four- to 16-fold) the global positive regulator gene, mga. Using a strain carrying a chromosomally integrated duplication of the nra 3' end and an nra-luciferase reporter gene transcriptional fusion, nra expression was observed to reach its maximum during late logarithmic growth phase, while no significant influence of atmospheric conditions could be distinguished clearly.
在对一株M49血清型A组链球菌(GAS)菌株的11.5 kb基因组区域进行测序时,鉴定出了一系列基因,包括nra(GAS的负调控因子)。对该区域的转录分析表明,nra主要以单顺反子形式转录。在nra下游的三个开放阅读框(ORF)和上游的四个ORF中发现了多顺反子表达。推导的Nra蛋白序列与GAS的RofA正调控因子具有62%的同源性。与RofA不同,通过对插入失活突变体的分析发现,Nra是其自身表达以及两个相邻操纵子表达的负调控因子。通过对10种不同GAS血清型的聚合酶链反应和杂交分析,证实了nra、rofA或两者在基因组中的存在。Nra调控的基因包括纤连蛋白结合蛋白F2基因(prtF2)和一种新型胶原结合蛋白(cpa)。Cpa多肽作为重组麦芽糖结合蛋白融合体被纯化,并显示其能结合I型胶原,但不能结合纤连蛋白。与nra作为prtF2和cpa的负调控因子一致,nra突变株与固定化胶原和纤连蛋白的附着水平高于野生型水平。此外,还发现nra对全局正调控因子基因mga也有负调控作用(4至16倍)。使用携带nra 3'末端染色体整合重复和nra - 荧光素酶报告基因转录融合的菌株,观察到nra表达在对数生长后期达到最大值,而未发现大气条件有明显显著影响。