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Mouse Hair Significantly Lightened Through Replacement of the Cysteine Residue in the N-Terminal Domain of Mc1r Using the CRISPR/Cas9 System

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/82865

Title: Mouse Hair Significantly Lightened Through Replacement of the Cysteine Residue in the N-Terminal Domain of Mc1r Using the CRISPR/Cas9 System
Authors: Suzuki, Hitoshi Browse this author →KAKEN DB
Kinoshita, Gohta Browse this author →KAKEN DB
Tsunoi, Takeru Browse this author
Noju, Koki Browse this author
Araki, Kimi Browse this author →KAKEN DB
Keywords: CRISPR/Cas9
hair color variant
loss of function
melanocortin 1 receptor
Issue Date: Oct-2020
Publisher: Oxford University Press
Journal Title: Journal of Heredity
Volume: 111
Issue: 7
Start Page: 640
End Page: 645
Publisher DOI: 10.1093/jhered/esaa054
Abstract: A loss-of-function mutation in the melanocortin 1 receptor gene (MC1R), which switches off the eumelanin production, causes yellowish coat color variants in mammals. In a wild population of sables (Martes zibellina) in Hokkaido, Japan, the mutation responsible for a bright yellow coat color variant was inferred to be a cysteine replacement at codon 35 of the N-terminal extracellular domain of the Mc1r receptor. In the present study, we validated these findings by applying genome editing on Mc1r in mouse strains C3H/HeJ and C57BL/6N, altering the codon for cysteine (Cys33Phe). The resulting single amino acid substitution (Cys33Phe) and unintentionally generated frameshift mutations yielded a color variant exhibiting substantially brighter body color, indicating that the Cys35 replacement produced sufficient MC1R loss of function to confirm that this mutation is responsible for producing the Hokkaido sable yellow color variant. Notably, the yellowish mutant mouse phenotype exhibited brown coloration in subapical hair on the dorsal side in both the C3H/HeJ and C57BL/6N strains, despite the inability of the latter to produce the agouti signaling protein (Asip). This darker hair and body coloration was not apparent in the Hokkaido sable variant, implying the presence of an additional genetic system shaping yellowish hair variability.
Rights: This is a pre-copyedited, author-produced version of an article accepted for publication in "Journal of Heredity" following peer review. The version of record "Journal of Heredity. 111(7), 2020, p.640–645" is available online at: https://doi.org/10.1093/jhered/esaa054
Type: article (author version)
URI: http://hdl.handle.net/2115/82865
Appears in Collections:環境科学院・地球環境科学研究院 (Graduate School of Environmental Science / Faculty of Environmental Earth Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 鈴木 仁

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