Thomas A, Lloyd R G
J Gen Microbiol. 1983 Mar;129(3):681-6. doi: 10.1099/00221287-129-3-681.
DNA repair and genetic recombination have been studied in recF143 mutants of Escherichia coli in which expression of inducible, SOS repair activities was altered by additional mutations either in lexA or recA. recF143 and lexA3 appeared to act additively to increase sensitivity to UV irradiation and to reduce recombination proficiency. The recF defect was suppressed in strains carrying the tif-1 allele of recA but not in strains carrying mutations that increased synthesis of recA+ protein or which directly inactivated lexA repressor. These and other data are interpreted to suggest that the recF defect is related to a reduced activity of recA protein. The implications of these findings are discussed in relation to the control of SOS activities and cell division during normal growth.
在大肠杆菌的recF143突变体中对DNA修复和基因重组进行了研究,在这些突变体中,诱导型SOS修复活性的表达因lexA或recA中的额外突变而发生改变。recF143和lexA3似乎具有累加作用,可增加对紫外线照射的敏感性并降低重组能力。recF缺陷在携带recA的tif-1等位基因的菌株中得到抑制,但在携带增加recA+蛋白合成的突变或直接使lexA阻遏物失活的突变的菌株中未得到抑制。这些以及其他数据被解释为表明recF缺陷与recA蛋白活性降低有关。结合正常生长过程中SOS活性和细胞分裂的控制对这些发现的意义进行了讨论。