Montandon Sophie A, Beaudier Pierre, Ullate-Agote Asier, Helleboid Pierre-Yves, Kummrow Maya, Roig-Puiggros Sergi, Jabaudon Denis, Andersson Leif, Milinkovitch Michel C, Tzika Athanasia C
Laboratory of Artificial and Natural Evolution, Department of Genetics & Evolution, University of Geneva, Geneva, Switzerland.
Present address: Bracco Suisse S.A., Plan-les-Ouates, Switzerland.
Genome Biol. 2025 Mar 26;26(1):73. doi: 10.1186/s13059-025-03539-0.
Snakes exhibit a broad variety of adaptive colors and color patterns, generated by the spatial arrangement of chromatophores, but little is known of the mechanisms responsible for these spectacular traits. Here, we investigate a mono-locus trait with two recessive alleles, motley and stripe, that both cause pattern aberrations in the corn snake.
We use mapping-by-sequencing to identify the genomic interval where the causal mutations reside. With our differential gene expression analyses, we find that CLCN2 (Chloride Voltage-Gated Channel 2), a gene within the genomic interval, is significantly downregulated in Motley embryonic skin. Furthermore, we identify the stripe allele as the insertion of an LTR-retrotransposon in CLCN2, resulting in a disruptive mutation of the protein. We confirm the involvement of CLCN2 in color pattern formation by producing knock-out snakes that present a phenotype similar to Stripe. In humans and mice, disruption of CLCN2 results in leukoencephalopathy, as well as retinal and testes degeneration. Our single-cell transcriptomic analyses in snakes reveal that CLCN2 is indeed expressed in chromatophores during embryogenesis and in the adult brain, but the behavior and fertility of Motley and Stripe corn snakes are not impacted.
Our genomic, transcriptomic, and functional analyses identify a plasma membrane anion channel to be involved in color pattern development in snakes and show that an active LTR-retrotransposon might be a key driver of trait diversification in corn snakes.
蛇类呈现出各种各样的适应性颜色和色彩图案,这些是由色素细胞的空间排列产生的,但对于这些惊人特征背后的机制却知之甚少。在这里,我们研究了一个单基因座性状,它有两个隐性等位基因,即杂色和条纹,这两个等位基因都会导致玉米蛇的图案畸变。
我们使用测序定位法来确定因果突变所在的基因组区间。通过差异基因表达分析,我们发现基因组区间内的一个基因CLCN2(氯离子电压门控通道2)在杂色胚胎皮肤中显著下调。此外,我们确定条纹等位基因是CLCN2中一个LTR反转录转座子的插入,导致蛋白质发生破坏性突变。我们通过培育出表现出与条纹蛇相似表型的基因敲除蛇,证实了CLCN2参与了色彩图案的形成。在人类和小鼠中,CLCN2的破坏会导致白质脑病以及视网膜和睾丸退化。我们对蛇进行的单细胞转录组分析表明,CLCN2在胚胎发育过程中确实在色素细胞中表达,在成年大脑中也有表达,但杂色和条纹玉米蛇的行为和生育能力并未受到影响。
我们的基因组、转录组和功能分析确定了一种质膜阴离子通道参与蛇类的色彩图案发育,并表明一个活跃的LTR反转录转座子可能是玉米蛇性状多样化的关键驱动因素。