mc1r的破坏扰乱了热带非洲爪蟾的皮肤色素沉着

IF 3.9 3区 医学 Q2 CELL BIOLOGY
Lanxin Li, Jixuan Huang, Yonglong Chen, Rensen Ran
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引用次数: 0

摘要

黑素皮质素1受体(MC1R)在许多物种中被认为是色素沉着的关键调节因子。尽管对哺乳动物和鱼类进行了大量的研究,但Mc1r在两栖动物中的作用在很大程度上仍未被探索。本研究旨在阐明Mc1r在热带非洲爪蟾中的作用。我们的研究结果表明,靶向消融热带非洲爪蟾mc1r导致背侧皮肤色素沉着显著减少,同时加速了腹侧区域黑色素沉着的发生。这种双重效应导致了规范反遮阳模式的扰动。此外,敲除mc1r破坏了主要与色素沉着相关的多个基因的表达。总的来说,这些发现强调了MC1R在两栖动物色素沉着调控和反遮光发育中的关键作用,有助于越来越多的关于MC1R在脊椎动物物种中的进化和功能的文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Disruption of mc1r Disturbs Skin Pigmentation in Xenopus tropicalis

The melanocortin 1 receptor (MC1R) is well-established as a pivotal regulator of pigmentation in various species. Despite a wealth of research focused on mammals and fish, the role of Mc1r in amphibians has remained largely unexplored. This study was designed to elucidate the contribution of Mc1r in Xenopus tropicalis. Our results reveal that targeted ablation of mc1r in Xenopus tropicalis led to a significant reduction in dorsal skin pigmentation, while simultaneously accelerating the onset of melanophore pigmentation in the ventral region. This dual effect resulted in a perturbation of the canonical countershading pattern. Additionally, knockout of mc1r disrupted the expression of multiple genes primarily associated with pigmentation. Collectively, these findings underscore the critical role of MC1R in the regulation of pigmentation and the development of countershading in amphibians, contributing to the growing body of literature on the evolution and function of MC1R across vertebrate species.

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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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