Lundrigan M D, Köster W, Kadner R J
Department of Microbiology, School of Medicine, University of Virginia, Charlottesville 22908.
Proc Natl Acad Sci U S A. 1991 Feb 15;88(4):1479-83. doi: 10.1073/pnas.88.4.1479.
The Escherichia coli btuB gene product is an outer membrane protein required for the active transport of vitamin B12 and other cobalamins. Synthesis of BtuB is repressed when cells are grown in the presence of cobalamins. Mapping of the 5' end of the btuB transcript revealed that a 240-nucleotide transcribed leader precedes the coding sequence. Point mutations causing increased expression under repressing conditions were isolated by use of a btuB-lacZ gene fusion. Mutations at many sites within the leader region affected btuB-lacZ regulation, whereas some base changes upstream of the start of transcription affected the absolute level of expression but not its repressibility. Analysis of btuB-phoA gene fusions and btuB-lacZ operon and gene fusions of various lengths showed that sequences within the btuB coding region (between nucleotides +250 and +350) had to be present for proper expression and transcriptional regulation. Sequences within the leader region (up to +250) conferred regulation of translational fusions. These results indicate that btuB expression is controlled at both the transcriptional and translational levels and that different but possibly overlapping sequences in the transcribed region, including the coding region for the transport protein itself, mediate these two modes of regulation.
大肠杆菌btuB基因产物是一种外膜蛋白,是维生素B12和其他钴胺素主动运输所必需的。当细胞在钴胺素存在的情况下生长时,BtuB的合成受到抑制。对btuB转录本5'端的定位显示,在编码序列之前有一个240个核苷酸的转录前导序列。通过使用btuB-lacZ基因融合,分离出了在抑制条件下导致表达增加的点突变。前导区内许多位点的突变影响了btuB-lacZ的调控,而转录起始点上游的一些碱基变化影响了表达的绝对水平,但不影响其可抑制性。对btuB-phoA基因融合以及不同长度的btuB-lacZ操纵子和基因融合的分析表明,btuB编码区内(核苷酸+250至+350之间)的序列必须存在才能实现正常表达和转录调控。前导区内(至+250)的序列赋予了翻译融合的调控。这些结果表明,btuB的表达在转录和翻译水平上均受到控制,并且转录区内不同但可能重叠的序列,包括转运蛋白本身的编码区,介导了这两种调控模式。