Loss-of-function mutations in the melanocortin 1 receptor cause disruption of dorso-ventral countershading in teleost fish

Laura Cal, Paula Suarez-Bregua, Ingo Braasch, Uwe Irion, Robert Kelsh, Jose Miguel Cerdá-Reverter, Josep Rotllant

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

The melanocortin 1 receptor (MC1R) is the central melanocortin receptor involved in vertebrate pigmentation. Mutations in this gene cause variations in coat coloration in amniotes. Additionally, in mammals MC1R is the main receptor for agouti-signaling protein (ASIP), making it the critical receptor for the establishment of dorsal-ventral countershading. In fish, Mc1r is also involved in pigmentation, but it has been almost exclusively studied in relation to melanosome dispersion activity and as a putative genetic factor involved in dark/light adaptation. However, its role as the crucial component for the Asip1-dependent control of dorsal-ventral pigmentation remains unexplored. Using CRISPR/Cas9, we created mc1r homozygous knockout zebrafish and found that loss-of-function of mc1r causes a reduction of countershading and a general paling of the animals. We find ectopic development of melanophores and xanthophores, accompanied by a decrease in iridophore numbers in the ventral region of mc1r mutants. We also reveal subtle differences in the role of mc1r in repressing pigment cell development between the skin and scale niches in ventral regions.

Original languageEnglish
Pages (from-to)817-828
Number of pages12
JournalPigment Cell and Melanoma Research
Volume32
Issue number6
Early online date28 Jun 2019
DOIs
Publication statusPublished - 1 Nov 2019

Keywords

  • Asip1
  • chromatophore
  • countershading
  • CRISPR
  • iridophores
  • Mc1r
  • melanophores
  • pigmentation
  • xanthophores
  • zebrafish

ASJC Scopus subject areas

  • Oncology
  • Biochemistry, Genetics and Molecular Biology(all)
  • Dermatology

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