Klug G, Adams C W, Belasco J, Doerge B, Cohen S N
Department of Genetics, Stanford University School of Medicine, CA 94305.
EMBO J. 1987 Nov;6(11):3515-20. doi: 10.1002/j.1460-2075.1987.tb02677.x.
It has been proposed that intercistronic stem and loop structures located in the puf operon of the photosynthetic bacterium Rhodobacter capsulatus account for segmental differences in transcript stability and consequently, the differential expression of the B870 and reaction center (RC) proteins encoded by puf. We report here that deletion of these structures leads to a failure to detect as discrete fragments the B870-encoding 0.49 kb and 0.50 kb mRNA segments located upstream from the site of the hairpins. The absence of these stable transcript fragments is associated with altered stoichiometry of the B870 and RC pigment-protein complexes in the bacterial intracytoplasmic membrane and a decreased rate of cell growth under photosynthetic conditions. These results support the view that the hairpin loop structures of the puf intercistronic region function in vivo to impede exoribonucleolytic degradation of upstream mRNA and establish that segmental variations in mRNA stability have a biologically important role in regulating the expression of puf operon genes.
有人提出,光合细菌荚膜红细菌(Rhodobacter capsulatus)的puf操纵子中的顺反子间茎环结构导致了转录本稳定性的片段差异,进而导致puf编码的B870和反应中心(RC)蛋白的差异表达。我们在此报告,删除这些结构会导致无法将位于发夹位点上游的编码B870的0.49 kb和0.50 kb mRNA片段检测为离散片段。这些稳定转录本片段的缺失与细菌胞内膜中B870和RC色素蛋白复合物的化学计量变化以及光合条件下细胞生长速率降低有关。这些结果支持了这样一种观点,即puf顺反子间区域的发夹环结构在体内起到阻碍上游mRNA外切核糖核酸酶降解的作用,并证实mRNA稳定性的片段变化在调节puf操纵子基因的表达中具有生物学重要作用。