Thomas C M
Plasmid. 1986 Jul;16(1):15-29. doi: 10.1016/0147-619x(86)90075-2.
Plasmid pRK2501 is a deletion derivative of broad host range plasmid RK2 and encodes two trfB-regulated operons: the trfA operon which codes for both kilD, which interferes with plasmid maintenance if unregulated, and trfA whose protein product(s) is essential for replication from oriVRK2; and part of the trfB operon, containing both trfB/korA/korD, whose product negatively regulates transcription of both trfA and trfB operons, and incC, the product of which interferes in trans with inheritance of RK2 and certain of its derivatives. Plasmid pRK2501ts3 is a derivative with a point mutation in trfB, rendering plasmid maintenance temperature sensitive. Transcriptional fusions of the trfB operon and the galK gene demonstrate that this mutation derepresses trfB operon transcription at both 30 and 42 degrees C. The trfA operon is also derepressed by this mutation. Since the trfB gene product appears to be defective at both permissive and non-permissive temperatures the temperature sensitivity of pRK2501ts3 must be due to a secondary effect. In fact, it appears to arise from the inhibitory behavior of derepressed incC at the non-permissive temperature since a major class of "revertant" of pRK2501ts3 contains deletions inactivating incC and a reconstruction experiment demonstrates that such a deletion is sufficient for "reversion." Maxicell experiments show that at the non-permissive temperature the trfA operon polypeptide products are produced at much lower levels, an effect partly reversed by a deletion affecting incC. It is proposed that incC normally plays a role in maintenance of IncP plasmids by modulation of trfA operon expression.
质粒pRK2501是广宿主范围质粒RK2的缺失衍生物,编码两个受trfB调控的操纵子:trfA操纵子,其编码kilD(如果不受调控会干扰质粒维持)和trfA(其蛋白质产物对于从oriVRK2复制至关重要);以及trfB操纵子的一部分,包含trfB/korA/korD(其产物对trfA和trfB操纵子的转录起负调控作用)和incC(其产物可反式干扰RK2及其某些衍生物的遗传)。质粒pRK2501ts3是trfB发生点突变的衍生物,使质粒维持呈现温度敏感性。trfB操纵子与galK基因的转录融合表明,该突变在30℃和42℃时均解除对trfB操纵子转录的抑制。trfA操纵子也因该突变而解除抑制。由于trfB基因产物在允许温度和非允许温度下似乎均有缺陷,pRK2501ts3的温度敏感性必定归因于二级效应。实际上,它似乎源于非允许温度下解除抑制的incC的抑制行为,因为pRK2501ts3的一大类“回复突变体”含有使incC失活的缺失,且一项重建实验表明这种缺失足以导致“回复突变”。大细胞实验表明,在非允许温度下,trfA操纵子的多肽产物产生水平低得多,影响incC的缺失可部分逆转这种效应。有人提出,incC通常通过调节trfA操纵子的表达在IncP质粒的维持中发挥作用。