Gosset Guillermo, Zhang Zhongge, Nayyar Samir, Cuevas William A, Saier Milton H
Division of Biological Sciences, University of California at San Diego, La Jolla, California 92093-0116, USA.
J Bacteriol. 2004 Jun;186(11):3516-24. doi: 10.1128/JB.186.11.3516-3524.2004.
We report here the transcriptome analyses of highly expressed genes that are subject to catabolite repression or activation mediated by the cyclic AMP receptor protein (Crp). The results reveal that many operons encoding enzymes of central carbon metabolic pathways (e.g., Krebs cycle enzymes), as well as transporters and enzymes that initiate carbon metabolism, are subject to direct Crp-mediated catabolite repression. By contrast, few enzyme-encoding genes (direct regulation) but many ribosomal protein- and tRNA-encoding genes (indirect regulation) are subject to Crp-dependent glucose activation. Additionally, Crp mediates strong indirect catabolite repression of many cytoplasmic stress response proteins, including the major chaperone proteins, five ATP-dependent protease complexes, and several cold and heat shock proteins. These results were confirmed by (i) phenotypic analyses, (ii) real-time PCR studies, (iii) reporter gene fusion assays, and (iv) previously published reports about representative genes. The results serve to define and extend our appreciation of the Crp regulon.
我们在此报告了对受环腺苷酸受体蛋白(Crp)介导的分解代谢物阻遏或激活作用的高表达基因的转录组分析。结果显示,许多编码中心碳代谢途径酶(如三羧酸循环酶)的操纵子,以及启动碳代谢的转运蛋白和酶,都受到Crp直接介导的分解代谢物阻遏作用。相比之下,很少有编码酶的基因(直接调控),但许多编码核糖体蛋白和tRNA的基因(间接调控)受到Crp依赖的葡萄糖激活作用。此外,Crp介导了对许多细胞质应激反应蛋白的强烈间接分解代谢物阻遏作用,包括主要的伴侣蛋白、五种ATP依赖的蛋白酶复合物以及几种冷休克和热休克蛋白。这些结果通过以下方式得到证实:(i)表型分析,(ii)实时PCR研究,(iii)报告基因融合分析,以及(iv)先前发表的关于代表性基因的报告。这些结果有助于定义和扩展我们对Crp调控子的认识。