Wainwright L A, Pritchard K H, Seifert H S
Department of Microbiology/Immunology, Northwestern University Medical School, Chicago, Illinois 60611.
Mol Microbiol. 1994 Jul;13(1):75-87. doi: 10.1111/j.1365-2958.1994.tb00403.x.
Antigenic variation of the Neisseria gonorrhoeae pilus occurs when a variant pilin sequence from a silent locus recombines into the expression locus by predominantly unidirectional, homologous recombination. At the 3' end of all pilin loci lies a conserved DNA sequence, called the Sma/Cla repeat, which has sequence similarity to several recombinase-binding sites, and therefore may be involved in pilin recombination. We have developed a novel reverse transcriptase/polymerase chain reaction (RT-PCR) assay for direct monitoring of pilin recombination, and both RT-PCR and phase variation were used to examine pilin recombination in a gonococcal strain that had had the pilE Sma/Cla repeat removed. Results from these experiments showed a decrease in pilin recombination when the Sma/Cla sequence was deleted from the expression locus, showing that a specialized site (Sma/Cla) is involved in efficient pilin recombination.
淋病奈瑟菌菌毛的抗原变异发生在来自沉默基因座的变异菌毛蛋白序列通过主要单向的同源重组重新组合到表达基因座时。在所有菌毛蛋白基因座的3'端存在一个保守的DNA序列,称为Sma/Cla重复序列,它与几个重组酶结合位点具有序列相似性,因此可能参与菌毛蛋白重组。我们开发了一种新型逆转录酶/聚合酶链反应(RT-PCR)检测方法,用于直接监测菌毛蛋白重组,并且使用RT-PCR和相变来检测去除了pilE Sma/Cla重复序列的淋球菌菌株中的菌毛蛋白重组。这些实验的结果表明,当从表达基因座中删除Sma/Cla序列时,菌毛蛋白重组减少,表明一个特化位点(Sma/Cla)参与了有效的菌毛蛋白重组。