Stern A, Brown M, Nickel P, Meyer T F
Cell. 1986 Oct 10;47(1):61-71. doi: 10.1016/0092-8674(86)90366-1.
The chromosome of N. gonorrhoeae contains several complete expression genes coding for variant opacity proteins. DNA sequence analysis of two opacity genes derived from the same locus (opaE1) of two isogenic gonococcal variants reveals common and variable regions in these genes. Genomic blotting experiments using synthetic probes suggest gene conversion as a principle for the assembly of variant sequence information in opacity genes. The 5' region of opacity genes is composed of identical pentameric pyrimidine units (CTCTT) encoding the hydrophobic portion of the opacity leader peptide. This coding repeat is variable in a given locus with respect of the number of pentameric units. While all expression loci in a single cell are constitutively transcribed, the production of opacity proteins is determined by the coding repeat sequence on the translational level.
淋病奈瑟菌的染色体包含几个编码可变不透明蛋白的完整表达基因。对来自两个同基因淋病奈瑟菌变体同一基因座(opaE1)的两个不透明基因进行DNA序列分析,揭示了这些基因中的共同区域和可变区域。使用合成探针的基因组印迹实验表明基因转换是不透明基因中可变序列信息组装的一个原理。不透明基因的5'区域由相同的五聚体嘧啶单元(CTCTT)组成,编码不透明前导肽的疏水部分。这种编码重复在给定基因座中五聚体单元的数量方面是可变的。虽然单个细胞中的所有表达基因座都是组成性转录的,但不透明蛋白的产生在翻译水平上由编码重复序列决定。