Nuzhdin S V, Reiwitch S G
Section of Evolution and Ecology, University of California at Davis, Davis, CA 95616, USA.
Heredity (Edinb). 2000 Jan;84 ( Pt 1):97-102. doi: 10.1038/sj.hdy.6886400.
The identification of genes contributing to speciation has the potential to provide important insights into the mechanisms of evolution. One of the most interesting unresolved puzzles is the relationship between intraspecific variability in morphological traits and their interspecific divergence. Intraspecific polymorphisms without major detrimental side-effects may serve as a substrate for selection response during speciation. The same quantitative trait loci (QTLs) may, then, account for the trait variability both within and between species. In contrast, the vast majority of intraspecific variants could be deleterious mutations that have not yet been selected out. In this case intraspecific variation would not ultimately generate interspecific trait differences. In previous work, QTLs responsible for morphological differences between animal species, including those for the secondary sexual trait sex comb tooth number, have been mapped with the resolution of chromosome segments. Here, we mapped QTLs for which alleles segregated between two laboratory lines of Drosophila melanogaster. The two QTLs identified mapped to the X chromosome and accounted for only 8% of the between-line differences, implying that a large number of small-effect genes modify sex combs. One intraspecific QTL mapped to the same interval as the QTL for interspecific differences between D. simulans and D. mauritiana. Whether or not these effects result from the same genes requires further examination.
鉴定促成物种形成的基因有可能为进化机制提供重要见解。最有趣的未解决谜题之一是形态性状的种内变异性与其种间差异之间的关系。没有重大有害副作用的种内多态性可能作为物种形成期间选择反应的底物。那么,相同的数量性状基因座(QTL)可能解释物种内部和物种之间的性状变异性。相比之下,绝大多数种内变异可能是尚未被淘汰的有害突变。在这种情况下,种内变异最终不会产生种间性状差异。在先前的工作中,已经以染色体片段的分辨率定位了负责动物物种之间形态差异的QTL,包括那些用于第二性征性梳齿数目的QTL。在这里,我们定位了在两个黑腹果蝇实验室品系之间等位基因分离的QTL。鉴定出的两个QTL定位于X染色体,仅占品系间差异的8%,这意味着大量小效应基因修饰性梳。一个种内QTL定位于与拟果蝇和毛里求斯果蝇种间差异的QTL相同的区间。这些效应是否由相同基因引起需要进一步研究。