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需要多个自发突变的适应性进化。I. 涉及插入序列的突变。

Adaptive evolution that requires multiple spontaneous mutations. I. Mutations involving an insertion sequence.

作者信息

Hall B G

机构信息

Molecular and Cell Biology, University of Connecticut, Storrs 06268.

出版信息

Genetics. 1988 Dec;120(4):887-97. doi: 10.1093/genetics/120.4.887.

Abstract

Escherichia coli K12 strain chi 342LD requires two mutations in the bgl (beta-glucosidase) operon, bglR0----bglR+ and excision of IS103 from within bglF, in order to utilize salicin. In growing cells the two mutations occur at rates of 4 x 10(-8) per cell division and less than 2 x 10(-12) per cell division, respectively. In 2-3-week-old colonies on MacConkey salicin plates the double mutants occur at frequencies of 10(-8) per cell, yet the rate of an unselected mutation, resistance to valine, is unaffected. The two mutations occur sequentially. Colonies that are 8-12 days old contain from 1% to about 10% IS103 excision mutants, from which the Sal+ secondary bglR0----bglR+ mutants arise. It is shown that the excision mutants are not advantageous within colonies; thus, they must result from a burst of independent excisions late in the life of the colony. Excision of IS103 occurs only on medium containing salicin, despite the fact that the excision itself confers no detectable selective advantage and serves only to create the potential for a secondary selectively advantageous mutation.

摘要

大肠杆菌K12菌株chi 342LD需要β-葡萄糖苷酶(bgl)操纵子发生两个突变,即bglR0转变为bglR+以及从bglF内部切除IS103,才能利用水杨苷。在生长的细胞中,这两个突变的发生率分别为每细胞分裂4×10⁻⁸次和每细胞分裂少于2×10⁻¹²次。在MacConkey水杨苷平板上2 - 3周龄的菌落中,双突变体的出现频率为每细胞10⁻⁸次,然而未选择的突变(对缬氨酸的抗性)发生率不受影响。这两个突变是顺序发生的。8 - 12日龄的菌落含有1%至约10%的IS103切除突变体,Sal+二级bglR0转变为bglR+突变体由此产生。结果表明,切除突变体在菌落内部并无优势;因此,它们必定是在菌落生命周期后期由一系列独立的切除事件导致的。IS103的切除仅发生在含有水杨苷的培养基上,尽管切除本身并未赋予可检测到的选择优势,只是为产生二级选择优势突变创造了可能性。

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本文引用的文献

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Spontaneous Mutation in Non-Dividing Bacteria.非分裂细菌中的自发突变。
Genetics. 1955 Sep;40(5):726-38. doi: 10.1093/genetics/40.5.726.
3
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IS1-mediated DNA rearrangements.IS1介导的DNA重排。
Cold Spring Harb Symp Quant Biol. 1981;45 Pt 1:93-8. doi: 10.1101/sqb.1981.045.01.017.
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Topological repression of gene activity by a transposable element.转座元件对基因活性的拓扑抑制作用。
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