Kaelin Christopher B, McGowan Kelly A, Trotman Joshaya C, Koroma Donald C, David Victor A, Menotti-Raymond Marilyn, Graff Emily C, Schmidt-Küntzel Anne, Oancea Elena, Barsh Gregory S
Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA; HudsonAlpha Institute for Biotechnology, Huntsville, AL 35806, USA.
Department of Neuroscience, Division of Biology and Medicine, Brown University, Providence, RI 02912, USA.
Curr Biol. 2025 Jun 23;35(12):2826-2836.e5. doi: 10.1016/j.cub.2025.04.055. Epub 2025 May 15.
The Sex-linked orange mutation in domestic cats causes variegated patches of reddish/yellow hair and is a defining signature of random X inactivation in female tortoiseshell and calico cats. Unlike the situation for most coat color genes, there is no apparent homolog for Sex-linked orange in other mammals. We show that Sex-linked orange is caused by a 5-kb deletion that leads to ectopic and melanocyte-specific expression of the Rho GTPase Activating Protein 36 (Arhgap36) gene. Single-cell RNA sequencing (RNA-seq) studies from fetal cat skin reveal that red/yellow hair color is caused by reduced expression of melanogenic genes that are normally activated by the melanocortin 1 receptor (Mc1r)-cyclic adenosine monophosphate (cAMP)-protein kinase A (PKA) pathway, but Mc1r and its ability to stimulate cAMP accumulation is intact. Instead, we show that expression of Arhgap36 in melanocytes leads to reduced levels of the PKA catalytic subunit (PKA); thus, Sex-linked orange is genetically and biochemically downstream of Mc1r. Our findings resolve a longstanding comparative genetic puzzle, provide in vivo evidence for the ability of Arhgap36 to inhibit PKA, and reveal a molecular explanation for a charismatic color pattern with a rich genetic history.
家猫的性连锁橙色突变会导致出现红/黄相间的斑驳毛色,这是雌性玳瑁猫和三色猫随机X染色体失活的一个典型特征。与大多数毛色基因的情况不同,在其他哺乳动物中没有明显的性连锁橙色基因的同源物。我们发现,性连锁橙色是由一个5kb的缺失引起的,该缺失导致Rho GTP酶激活蛋白36(Arhgap36)基因在黑素细胞中异位且特异性表达。对胎儿猫皮肤进行的单细胞RNA测序(RNA-seq)研究表明,红/黄毛色是由黑色素生成基因表达减少所致,这些基因通常由黑皮质素1受体(Mc1r)-环磷酸腺苷(cAMP)-蛋白激酶A(PKA)途径激活,但Mc1r及其刺激cAMP积累的能力是完整的。相反,我们发现Arhgap36在黑素细胞中的表达导致PKA催化亚基(PKA)水平降低;因此,性连锁橙色在遗传和生化层面上位于Mc1r的下游。我们的研究结果解决了一个长期存在的比较遗传学难题,为Arhgap36抑制PKA的能力提供了体内证据,并揭示了一种具有丰富遗传历史的迷人毛色模式的分子解释。
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