2018
DOI: 10.1016/j.gene.2018.04.054
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Dynamic regulation of mRNA and miRNA associated with the developmental stages of skin pigmentation in Japanese ornamental carp

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Cited by 29 publications
(16 citation statements)
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“…Coloration is determined mainly by diverse pigments synthesized by pigment cells that are developed and differentiated from neural crest cells during embryonic development 3 . Unlike mammals, in which only melanophores (black or brown) are present, and amphibians and reptiles which possess xanthophores (yellow), erythrophores (red or orange), and iridophores (reflecting), six types of pigment cells, namely melanophores, xanthophores, erythrophores, iridophores, leucophores (white), and cyanophores (blue), have been identified in teleosts based on their hue, implying great plasticity in skin coloration 4 . Owing to the diversity of pigment cells in fish, skin color has become an essential phenotypic characteristic that assists the breeding of high yield and superior quality, and helps increase economic value 5 .…”
Section: Introductionmentioning
confidence: 99%
“…Coloration is determined mainly by diverse pigments synthesized by pigment cells that are developed and differentiated from neural crest cells during embryonic development 3 . Unlike mammals, in which only melanophores (black or brown) are present, and amphibians and reptiles which possess xanthophores (yellow), erythrophores (red or orange), and iridophores (reflecting), six types of pigment cells, namely melanophores, xanthophores, erythrophores, iridophores, leucophores (white), and cyanophores (blue), have been identified in teleosts based on their hue, implying great plasticity in skin coloration 4 . Owing to the diversity of pigment cells in fish, skin color has become an essential phenotypic characteristic that assists the breeding of high yield and superior quality, and helps increase economic value 5 .…”
Section: Introductionmentioning
confidence: 99%
“…For example, BCO2 encodes a carotenoid-cleavage enzyme which is associated with yellow/white skin and plumage color polymorphism in birds [18,19]; CYP2J19 encodes a ketolase that catalyzes the metabolic conversion of dietary yellow carotenoids into red ketocarotenoids in birds and turtles [20][21][22]; SCARB1 encodes a high-density lipoprotein receptor that mediates the cellular uptake of carotenoids and was found to be responsible for the presence/absence of carotenoid plumage coloration in canary breeds [23]. Comparative transcriptomic analyses revealed correlations between carotenoidbased skin color differences and the expression levels of some of the known carotenoid color genes, and identified novel candidate genes which might be involved in carotenoid-based coloration (e.g., [24][25][26][27][28]). In the present study, we used RNA sequencing (RNA-Seq) to test for differential gene expression associated with the presence/absence of carotenoid-based coloration in a cichlid fish.…”
Section: Introductionmentioning
confidence: 99%
“…Recent studies demonstrated that the expression profiles of miRNA showed tissue-specific expression patterns in the epidermis hair follicles, stage-specific expression in the periodic development of hair follicles as well as pigmentation [26][27][28]. miRNAs in different cell types form a comprehensive, multi-level network system through interactions with signal pathway and regulation factors [29,30].…”
Section: Discussionmentioning
confidence: 99%