G B Ruvkun, S R Long, H M Meade, R C van den Bos, F M Ausubel
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引用次数: 0
摘要
转座子Tn5诱变后,很大比例的梅氏根瘤菌共生突变体在共生基因中不含Tn5插入。相反,这些菌株的突变与固氮基因(nif)或与nif基因相邻的共生基因中内源性插入序列(ISRm1)的存在有关。ISRm1是1.4 kb,在nif区以10(-2)和10(-3)之间的频率转置到至少3个限制性片段。从无法共生固定氮(fix -)的突变株中克隆出含有ISRm1的nif区限制性片段,并将所得到的质粒用作杂交探针。ISRm1在R. meliloti基因组中至少存在10次,但在任何其他R. meliloti菌株,大肠杆菌菌株或根瘤菌中均不存在。我们通过将含有ISRm1的克隆片段偶联到野生型Fix+ R. meliloti宿主中,并用nif::ISRm1片段替换正常基因组的nif片段,证明了与ISRm1转位相关的Fix-表型确实是由ISRm1插入引起的。得到的菌株是Fix-。
ISRm1: A Rhizobium meliloti insertion sequence that transposes preferentially into nitrogen fixation genes.
After transposon Tn5 mutagenesis, a high proportion of Rhizobium meliloti symbiotic mutants do not contain Tn5 insertions in symbiotic genes. Instead, the mutations in these strains are correlated with the presence of an endogenous insertion sequence (ISRm1) in nitrogen fixation (nif) or symbiotic genes which are adjacent to the nif genes. ISRm1 is 1.4 kb and transposes to at least three restriction fragments in the nif region at a frequency between 10(-2) and 10(-3). A nif region restriction fragment containing ISRm1 was cloned from one of the mutant strains unable to fix nitrogen symbiotically (Fix-) and the resulting plasmid was used as a hybridization probe. ISRm1 is present at least ten times in the R. meliloti genome but is not present in any other R. meliloti strains, E. coli strains, or Rhizobium species tested. We demonstrated that the Fix- phenotype correlated with ISRm1 transposition is indeed caused by ISRm1 insertion by conjugating a cloned fragment containing ISRm1 into a wild type Fix+ R. meliloti host and replacing the normal genomic nif fragment with the nif::ISRm1 fragment. The resulting strain was Fix-.