Physiological and Evolutionary Genomics Laboratory, School of Biology, Scottish Oceans Institute, University of St Andrews, St Andrews, Fife, United Kingdom.
Mol Biol Evol. 2010 Aug;27(8):1886-902. doi: 10.1093/molbev/msq071. Epub 2010 Mar 11.
The most studied members of the calpain protease superfamily are CAPN1 and 2, which are conserved across vertebrates. Another similar family member called mu/m-CAPN has been identified in birds alone. Here, we establish that mu/m-CAPN shares one-to-one orthology with CAPN11, previously described only in eutherians (placental mammals). We use the name CAPN11 for this family member and identify orthologues across vertebrate lineages, which form a monophyletic phylogenetic clade directly ancestral to CAPN1 and 2. In lineages branching before therians (live-bearing mammals), the CAPN11 coding region has evolved under strong purifying selection, with low nonsynonymous (d(N)) versus synonymous (d(S)) substitution rates (d(N)/d(S) = 0.076 across pretherians), and its transcripts were detected widely across different tissues. These characteristics are present in CAPN1 and 2 across vertebrate lineages and indicate that pretherian CAPN11 likewise has conserved a wide physiological function. However, an approximately 7-fold elevation in d(N)/d(S) is evident along the CAPN11 branch splitting eutherians from platypus, paralleled by a shift to "testis-specific" gene regulation. Estimates of d(N)/d(S) in eutherians were approximately 3-fold elevated compared with pretherians and coding and transcriptional-level evidence suggests that CAPN11 is functionally absent in marsupials. Many CAPN11 sites are functionally constrained in eutherians to conserve a residue with radically different biochemical properties to a fixed state shared between pretherian CAPN11 and CAPN1 and 2. Protein homology modeling demonstrated that many such eutherian-specific residue replacements modify or ablate interactions with the calpain inhibitor calpastatin that are observed in both pretherian orthologues and CAPN1/2. We propose a model akin to the Dykhuizen-Hartl effect, where inefficient purifying selection and increased genetic drift associated with a reduction in effective population size, drove the fixation of mutations in regulatory and coding regions of CAPN11 of a common marsupial-eutherian ancestor. A subset of these changes had a cumulative adaptive advantage in a eutherian ancestor because of lineage-specific aspects of sperm physiology, whereas in marsupials, no advantage was realized and the gene was disabled. This work supports that functional divergence among gene family member orthologues is possible in the absence of widespread positive selection.
钙蛋白酶蛋白酶超家族中研究最多的成员是 CAPN1 和 CAPN2,它们在脊椎动物中是保守的。另一种类似的家族成员 mu/m-CAPN 仅在鸟类中被发现。在这里,我们确定 mu/m-CAPN 与 CAPN11 具有一一对应关系,CAPN11 以前仅在真兽类(胎盘哺乳动物)中被描述。我们将这个家族成员命名为 CAPN11,并在脊椎动物谱系中鉴定了其同源物,它们形成了一个直接祖先是 CAPN1 和 CAPN2 的单系进化枝。在真兽类(有胎盘哺乳动物)分支之前的谱系中,CAPN11 编码区受到强烈的净化选择,非同义(d(N))与同义(d(S))取代率(d(N)/d(S) 在 pretherians 中为 0.076)较低,其转录本在不同组织中广泛检测到。这些特征在脊椎动物谱系中的 CAPN1 和 CAPN2 中都存在,并表明 pretherian CAPN11 同样具有保守的广泛生理功能。然而,CAPN11 分支从鸭嘴兽中分离出真兽类时,d(N)/d(S) 升高了约 7 倍,同时基因调控转向“睾丸特异性”。与 pretherians 相比,真兽类的 d(N)/d(S) 估计值升高了约 3 倍,并且编码和转录水平的证据表明,CAPN11 在有袋类动物中没有功能。许多 CAPN11 位点在真兽类中受到功能限制,以保守一种具有根本不同生化特性的残基处于 pretherian CAPN11 和 CAPN1 和 CAPN2 之间的固定状态。蛋白质同源建模表明,许多这样的真兽类特异性残基替换改变或消除了与钙蛋白酶抑制剂钙蛋白酶抑制蛋白的相互作用,这种相互作用在 pretherian 同源物和 CAPN1/2 中都观察到。我们提出了一个类似于 Dykhuizen-Hartl 效应的模型,其中与有效种群大小减少相关的低效净化选择和遗传漂变导致了 CAPN11 调控和编码区突变的固定。这些变化中的一部分在真兽类祖先中具有累积的适应性优势,因为精子生理学具有谱系特异性方面,而在有袋类动物中,没有实现优势,并且该基因失活。这项工作支持在没有广泛正选择的情况下,基因家族成员同源物之间的功能分化是可能的。