Hendrickson Heather, Slechta E Susan, Bergthorsson Ulfar, Andersson Dan I, Roth John R
Department of Biology, University of Utah, Salt Lake City, UT 84112, USA.
Proc Natl Acad Sci U S A. 2002 Feb 19;99(4):2164-9. doi: 10.1073/pnas.032680899. Epub 2002 Feb 5.
When a particular lac mutant of Escherichia coli starves in the presence of lactose, nongrowing cells appear to direct mutations preferentially to sites that allow growth (adaptive mutation). This observation suggested that growth limitation stimulates mutability. Evidence is provided here that this behavior is actually caused by a standard Darwinian process in which natural selection acts in three sequential steps. First, growth limitation favors growth of a subpopulation with an amplification of the mutant lac gene; next, it favors cells with a lac(+) revertant allele within the amplified array. Finally, it favors loss of mutant copies until a stable haploid lac(+) revertant arises and overgrows the colony. By increasing the lac copy number, selection enhances the likelihood of reversion within each developing clone. This sequence of events appears to direct mutations to useful sites. General mutagenesis is a side-effect of growth with an amplification (SOS induction). The F' plasmid, which carries lac, contributes by stimulating gene duplication and amplification. Selective stress has no direct effect on mutation rate or target specificity, but acts to favor a succession of cell types with progressively improved growth on lactose. The sequence of events--amplification, mutation, segregation--may help to explain both the origins of some cancers and the evolution of new genes under selection.
当大肠杆菌的一种特定乳糖突变体在乳糖存在的情况下挨饿时,不生长的细胞似乎优先将突变导向允许生长的位点(适应性突变)。这一观察结果表明生长限制会刺激突变率。本文提供的证据表明,这种行为实际上是由一个标准的达尔文过程引起的,在这个过程中自然选择按三个连续步骤起作用。首先,生长限制有利于具有突变乳糖基因扩增的亚群的生长;其次,它有利于扩增阵列中具有乳糖(+)回复等位基因的细胞。最后,它有利于突变拷贝的丢失,直到稳定的单倍体乳糖(+)回复体出现并在菌落中占优势生长。通过增加乳糖拷贝数,选择增加了每个发育中的克隆内回复的可能性。这一系列事件似乎将突变导向有用的位点。一般诱变是扩增生长的副作用(SOS诱导)。携带乳糖的F'质粒通过刺激基因复制和扩增起作用。选择性压力对突变率或靶标特异性没有直接影响,但有利于一系列在乳糖上生长逐渐改善的细胞类型。扩增、突变、分离这一系列事件可能有助于解释某些癌症的起源以及选择作用下新基因的进化。