Duda T F, Palumbi S R
Department of Organismic and Evolutionary Biology, Biological Laboratories, Harvard University, USA.
Mol Biol Evol. 2000 Sep;17(9):1286-93. doi: 10.1093/oxfordjournals.molbev.a026412.
In order to investigate the evolution of conotoxin multigene families among two closely related vermivorous CONUS: species, we sequenced 104 four-loop conotoxin mRNAs from two individuals of CONUS: ebraeus and compared these with sequences already obtained from CONUS: abbreviatus. In contrast to the diversity of conotoxin sequences obtained from C. abbreviatus, only two common sequence variants were recovered from C. ebraeus. Segregation patterns of the variants in these two individuals and restriction digests of four-loop conotoxin amplification products from nine additional individuals suggest that the common variants are alleles from a single locus. These two putative alleles differ at nine positions that occur nonrandomly in the toxin-coding region of the sequences. Moreover, all substitutions are at nonsynonymous sites and are responsible for seven amino acid differences among the predicted amino acid sequences of the alleles. These results imply that conotoxin diversity is driven by strong diversifying selection and some form of frequency-dependent or overdominant selection at conotoxin loci, and they suggest that diverse conotoxin multigene families can originate from duplications at polymorphic loci. Furthermore, none of the sequences recovered from C. ebraeus appeared to be orthologs of loci from C. abbreviatus, and attempts to amplify orthologous sequences with locus-specific primers were unsuccessful among these species. These patterns suggest that venoms of closely related CONUS: species may differ due to the differential expression of conotoxin loci.
为了研究两种亲缘关系密切的食虫芋螺属物种中芋螺毒素多基因家族的进化情况,我们对来自细纹芋螺两个个体的104个四环芋螺毒素mRNA进行了测序,并将这些序列与已从简略芋螺获得的序列进行比较。与从简略芋螺获得的芋螺毒素序列的多样性不同,从细纹芋螺中仅回收了两个常见的序列变体。这两个个体中变体的分离模式以及来自另外九个个体的四环芋螺毒素扩增产物的限制性酶切分析表明,这些常见变体是来自单个位点的等位基因。这两个推定的等位基因在序列的毒素编码区域中九个非随机出现的位置上存在差异。此外,所有替换都发生在非同义位点,并且导致等位基因预测氨基酸序列之间有七个氨基酸差异。这些结果意味着芋螺毒素的多样性是由强烈的多样化选择以及芋螺毒素位点上某种形式的频率依赖性或超显性选择驱动的,并且表明多样的芋螺毒素多基因家族可能起源于多态性位点的重复。此外,从细纹芋螺中回收的序列似乎都不是简略芋螺位点的直系同源物,并且在这些物种中使用位点特异性引物扩增直系同源序列的尝试未成功。这些模式表明,亲缘关系密切的芋螺属物种的毒液可能因芋螺毒素位点的差异表达而有所不同。