School of Biological Sciences, Monash University, Melbourne, VIC 3800, Australia.
Evolution of Sensory and Physiological Systems, Max Planck Institute for Biological Intelligence, 82319, Seewiesen, Germany.
Heredity (Edinb). 2024 Nov;133(5):342-354. doi: 10.1038/s41437-024-00718-w. Epub 2024 Aug 22.
There is considerable evidence for mitochondrial-nuclear co-adaptation as a key evolutionary driver. Hypotheses regarding the roles of sex-linkage have emphasized Z-linked nuclear genes with mitochondrial function (N-mt genes), whereas it remains contentious whether the perfect co-inheritance of W genes with mitogenomes could hinder or facilitate co-adaptation. Young (neo-) sex chromosomes that possess relatively many N-mt genes compared to older chromosomes provide unprecedented hypothesis-testing opportunities. Eastern Yellow Robin (EYR) lineages in coastal and inland habitats with different climates are diverged in mitogenomes, and in a ~ 15.4 Mb nuclear region enriched with N-mt genes, in contrast with otherwise-similar nuclear genomes. This nuclear region maps to passerine chromosome 1A, previously found to be neo-sex in the inland EYR genome. To compare sex-linked Chr1A-derived genes between lineages, we assembled and annotated the coastal EYR genome. We found that: (i) the coastal lineage shares a similar neo-sex system with the inland lineage, (ii) neo-W and neo-Z N-mt genes are not more diverged between lineages than are comparable non-N-mt genes, and showed little evidence for broad positive selection, (iii) however, W-linked N-mt genes are more diverged between lineages than are their Z-linked gametologs. The latter effect was ~7 times stronger for N-mt than non-N-mt genes, suggesting that W-linked N-mt genes might have diverged between lineages under environmental selection through co-evolution with mitogenomes. Finally, we identify a candidate gene driver for divergent selection, NDUFA12. Our data represent a rare example suggesting a possible role for W-associated mitochondrial-nuclear interactions in climate-associated adaptation and lineage differentiation.
有大量证据表明线粒体-核共同适应是一个关键的进化驱动力。关于性连锁作用的假设强调了与线粒体功能相关的 Z 连锁核基因(N-mt 基因),而 W 基因与线粒体基因组的完美共同遗传是否会阻碍或促进共同适应仍然存在争议。与较老的染色体相比,拥有相对较多 N-mt 基因的年轻(新)性染色体为提供了前所未有的假设检验机会。沿海和内陆栖息地的东部黄鹀(EYR)谱系在不同气候的情况下在线粒体基因组中分化,并且在一个富含 N-mt 基因的约 15.4Mb 核区域中分化,而核基因组则相似。这个核区域映射到雀形目染色体 1A,之前在内陆 EYR 基因组中发现它是新性染色体。为了比较谱系之间的性连锁 Chr1A 衍生基因,我们组装并注释了沿海 EYR 基因组。我们发现:(i)沿海谱系与内陆谱系共享相似的新性系统,(ii)新 W 和新 Z N-mt 基因在谱系之间的分化程度并不高于可比的非 N-mt 基因,并且几乎没有广泛的正选择证据,(iii)然而,W 连锁的 N-mt 基因在谱系之间的分化程度高于其 Z 连锁的配子同源基因。与非 N-mt 基因相比,后者的影响强约 7 倍,这表明 W 连锁的 N-mt 基因可能在环境选择下通过与线粒体基因组的共同进化在谱系之间发生分化。最后,我们确定了一个候选基因驱动因子,NDUFA12。我们的数据代表了一个罕见的例子,表明 W 相关的线粒体-核相互作用可能在与气候相关的适应和谱系分化中发挥作用。