Gardel C, Johnson K, Jacq A, Beckwith J
Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, MA 02115.
EMBO J. 1990 Oct;9(10):3209-16. doi: 10.1002/j.1460-2075.1990.tb07519.x.
Cold-sensitive mutations in the secD locus of Escherichia coli result in severe defects in protein export at the non-permissive temperature of 23 degrees C. DNA sequence of a cloned fragment that includes the secD locus reveals open reading frames for seven polypeptide chains. Both deletions and TnphoA insertions in this clone have been used in maxicell and complementation studies to define the secD locus and its products. The secD mutations fall into two complementation groups, defining genes we have named secD and secF. These two genes comprise an operon, the first case of two genes involved in the export process being co-transcribed. The DNA sequence of the two genes along with alkaline phosphatase fusion analysis indicates that they code for integral proteins of the cytoplasmic membrane. We suggest that these two proteins may form a complex in the membrane which acts at late steps in the export process.
大肠杆菌secD基因座中的冷敏感突变在23摄氏度的非允许温度下导致蛋白质输出出现严重缺陷。包含secD基因座的克隆片段的DNA序列揭示了七条多肽链的开放阅读框。该克隆中的缺失和TnphoA插入已用于大细胞和互补研究,以定义secD基因座及其产物。secD突变分为两个互补组,定义了我们命名为secD和secF的基因。这两个基因组成一个操纵子,这是参与输出过程的两个基因共转录的首例情况。这两个基因的DNA序列以及碱性磷酸酶融合分析表明,它们编码细胞质膜的整合蛋白。我们认为这两种蛋白质可能在膜中形成复合物,在输出过程的后期发挥作用。