López de Felipe F, Magni C, de Mendoza D, López P
Centro de Investigaciones Biológicas, C.S.I.C., Velázquez, Madrid, Spain.
Mol Gen Genet. 1995 Mar 10;246(5):590-9. doi: 10.1007/BF00298965.
The transport of citrate in Lactococcus lactis biovar diacetylactis is mediated by the citrate permease P. This polypeptide is encoded by the citP gene carried by plasmid pCIT264. In this report, we characterize the citP transcript, identify a cluster of two genes cotranscribed with citP and describe their post-transcriptional regulation. The transcriptional promoter is located 1500 nucleotides upstream of the citP gene and the transcriptional terminator is positioned next to the 3'-end of this gene. The DNA sequence was determined of the region upstream of the citP gene, including the promoter. Two partially overlapping open reading frames, citQ and citR were identified, which could encode polypeptides of 3.9 and 13 kDa respectively. These two genes, together with citP, constitute the cit cluster. Moreover, an IS-like element located between the cit promoter and the citQ open reading frame was identified. This element includes an open reading frame ORF1, which could encode a 33 kDa polypeptide. A translational fusion between the citP and a cat reporter gene showed that translation of citR and citP is coupled, and regulated by CitR. The cit mRNA was subjected to specific cleavage after addition of rifampicin to the bacterial cultures. We propose that expression of the cit cluster is controlled at the post-transcriptional level by mRNA processing at a putative complex secondary structure and by translational repression mediated by CitR.
乳酸乳球菌双乙酰变种中柠檬酸盐的转运由柠檬酸盐通透酶P介导。该多肽由质粒pCIT264携带的citP基因编码。在本报告中,我们对citP转录本进行了表征,鉴定了与citP共转录的两个基因簇,并描述了它们的转录后调控。转录启动子位于citP基因上游1500个核苷酸处,转录终止子位于该基因3'端旁边。测定了citP基因上游区域(包括启动子)的DNA序列。鉴定出两个部分重叠的开放阅读框citQ和citR,它们分别可编码3.9 kDa和13 kDa的多肽。这两个基因与citP一起构成了cit基因簇。此外,在cit启动子和citQ开放阅读框之间鉴定出一个类IS元件。该元件包括一个开放阅读框ORF1,它可编码一个33 kDa的多肽。citP与cat报告基因之间的翻译融合表明,citR和citP的翻译是偶联的,并受CitR调控。在向细菌培养物中添加利福平后,cit mRNA发生特异性切割。我们提出,cit基因簇的表达在转录后水平上受假定复杂二级结构处的mRNA加工以及CitR介导的翻译抑制的控制。