Slc45a2 and V-ATPase are regulators of melanosomal pH homeostasis in zebrafish, providing a mechanism for human pigment evolution and disease

被引:104
作者
Dooley, Christopher M. [1 ]
Schwarz, Heinz [1 ]
Mueller, Kaspar P. [2 ]
Mongera, Alessandro [1 ]
Konantz, Martina [1 ]
Neuhauss, Stephan C. F. [2 ]
Nuesslein-Volhard, Christiane [1 ]
Geisler, Robert [1 ]
机构
[1] Max Planck Inst Dev Biol, Tubingen, Germany
[2] Univ Zurich, Inst Mol Life Sci, Zurich, Switzerland
关键词
slc45a2; albinism; V-ATPase; melanosome; melanocyte; retinal pigment epithelium; skin color variation; OCULOCUTANEOUS ALBINISM; GENE; MUTATIONS; IDENTIFICATION; POLYMORPHISMS; TYROSINASE; ORGANELLES; EXCHANGER; MUTANTS; PROTEIN;
D O I
10.1111/pcmr.12053
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We present here the positional cloning of the Danio rerio albino mutant and show that the affected gene encodes Slc45a2. The human orthologous gene has previously been shown to be involved in human skin color variation, and mutations therein have been implicated in the disease OCA4. Through ultrastructural analysis of the melanosomes in albino alleles as well as the tyrosinase-deficient mutant sandy, we add new insights into the role of Slc45a2 in the production of melanin. To gain further understanding of the role of Slc45a2 and its possible interactions with other proteins involved in melanization, we further analyzed the role of the V-ATPase as a melanosomal acidifier. We show that it is possible to rescue the melanization potential of the albino melanosomes through genetic and chemical inhibition of V-ATPase, thereby increasing internal melanosome pH.
引用
收藏
页码:205 / 217
页数:14
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