Sadosky A B, Davidson A, Lin R J, Hill C W
Department of Biological Chemistry, Milton S. Hershey Medical Center, Pennsylvania State University, Hershey 17033.
J Bacteriol. 1989 Feb;171(2):636-42. doi: 10.1128/jb.171.2.636-642.1989.
Two additional members of a novel Escherichia coli gene family, the rhs genes, have been cloned and characterized. The structures of these loci, rhsC and rhsD, have been compared with those of rhsA and rhsB. All four loci contain a homologous 3.7-kilobase-pair core. Sequence comparison of the first 300 nucleotides of the cores showed that rhsA, rhsB, and rhsC are closely related, with only 1 to 2% sequence divergence, whereas rhsD is 18% divergent from the others. The beginning of the core coincides with the initiation of an open reading frame that extends beyond the 300 nucleotides compared. Whether a protein product is produced from this open reading frame has not been established. However, nucleotide substitutions which differentiate the cores have highly conservative effects on the predicted protein products; this suggests that products are made from the open reading frame and are under severe selection. The four rhs loci have been placed on both the genetic and restriction maps of E. coli K-12. A fifth rhs locus remains to be characterized. In terms of size, number, and sequence conservation, the rhs genes make up one of the most significant repetitions in E. coli, comparable to the rRNA operons.
已克隆并鉴定了新型大肠杆菌基因家族(rhs基因)的另外两个成员。已将这些基因座(rhsC和rhsD)的结构与rhsA和rhsB的结构进行了比较。所有四个基因座都包含一个同源的3.7千碱基对核心。对核心的前300个核苷酸进行序列比较表明,rhsA、rhsB和rhsC密切相关,序列差异仅为1%至2%,而rhsD与其他基因座的差异为18%。核心的起始与一个开放阅读框的起始重合,该开放阅读框延伸超过了所比较的300个核苷酸。尚未确定是否从这个开放阅读框产生蛋白质产物。然而,区分核心的核苷酸替换对预测的蛋白质产物具有高度保守的影响;这表明产物是由开放阅读框产生的,并且受到严格的选择。这四个rhs基因座已定位在大肠杆菌K-12的遗传图谱和限制性图谱上。第五个rhs基因座有待鉴定。就大小、数量和序列保守性而言,rhs基因构成了大肠杆菌中最显著的重复序列之一,与rRNA操纵子相当。