A Dominant Mutation in Gαs-Protein Increases Hair Pigmentation

IF 3.9 3区 医学 Q2 CELL BIOLOGY
Philip S. Goff, Peter Budd, Darren W. Logan, Margaret Keighren, Marta Cantero, Lisa McKie, Lluis Montoliu, Ian J. Jackson, Elena V. Sviderskaya
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Abstract

We have identified a chemically induced mouse mutation which increases the eumelanic hair pigmentation. We identify a coding mutation, A3533G, resulting in an amino acid substitution Y1133C, in the Gnas gene encoding the Gαs subunit of the tripartite G-protein, consistent with an activation of signalling via MC1R. In addition heterozygous mutant females are significantly lighter than wild type littermates. In cultured melanocytes, derived from mutant mice crossed to C57BL6 mice carrying Cdkn2atm1Rdp, basal pigmentation is higher than wild type melanocytes derived from litter mates. However, the addition of exogenous NDP-MSH does not increase pigmentation in mutant melanocytes in contrast to the pigmentation response of non-mutant melanocytes. The mutant and wild type cells respond in the same way to agouti signalling protein (ASP), consistent with ASP signalling mediated through a pathway other than Gαs-protein.

Abstract Image

g αs蛋白的显性突变增加头发色素沉着
我们已经确定了一种化学诱导的小鼠突变,它增加了黑色素头发的色素沉着。我们在编码三方g蛋白Gαs亚基的Gnas基因中发现了一个编码突变A3533G,导致氨基酸替换Y1133C,这与通过MC1R激活信号一致。此外,杂合突变雌鼠的体重明显低于野生型雌鼠。在与携带Cdkn2atm1Rdp的突变小鼠杂交的C57BL6小鼠培养的黑素细胞中,基底色素沉着高于来自产仔配偶的野生型黑素细胞。然而,与非突变黑色素细胞的色素沉着反应相比,外源性NDP-MSH的加入并不会增加突变黑色素细胞的色素沉着。突变型细胞和野生型细胞对agouti信号蛋白(ASP)的响应方式相同,与ASP信号通过g - α - s蛋白以外的途径介导一致。
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来源期刊
Pigment Cell & Melanoma Research
Pigment Cell & Melanoma Research 医学-皮肤病学
CiteScore
8.90
自引率
2.30%
发文量
54
审稿时长
6-12 weeks
期刊介绍: Pigment Cell & Melanoma Researchpublishes manuscripts on all aspects of pigment cells including development, cell and molecular biology, genetics, diseases of pigment cells including melanoma. Papers that provide insights into the causes and progression of melanoma including the process of metastasis and invasion, proliferation, senescence, apoptosis or gene regulation are especially welcome, as are papers that use the melanocyte system to answer questions of general biological relevance. Papers that are purely descriptive or make only minor advances to our knowledge of pigment cells or melanoma in particular are not suitable for this journal. Keywords Pigment Cell & Melanoma Research, cell biology, melatonin, biochemistry, chemistry, comparative biology, dermatology, developmental biology, genetics, hormones, intracellular signalling, melanoma, molecular biology, ocular and extracutaneous melanin, pharmacology, photobiology, physics, pigmentary disorders
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