GEPHE SUMMARY Print
Gephebase Gene
Entry Status
Published
GepheID
GP00001955
Main curator
Courtier
PHENOTYPIC CHANGE
Trait Category
Trait State in Taxon A
wild-type coloration
Trait State in Taxon B
absence of all black and brown pigmentation in the skin; iris and retina
Ancestral State
Taxon A
Taxonomic Status
Taxon A
Common Name
-
Synonyms
Chromis auratus; Tilapia aurea; golden mbuna; Melanochromis auratus (Boulenger, 1897)
Rank
species
Lineage
Show more ... ypterygia; Ctenosquamata; Acanthomorphata; Euacanthomorphacea; Percomorphaceae; Ovalentaria; Cichlomorphae; Cichliformes; Cichlidae; African cichlids; Pseudocrenilabrinae; Haplochromini; Melanochromis
NCBI Taxonomy ID
is Taxon A an Infraspecies?
No
Taxon B
Common Name
-
Synonyms
Chromis auratus; Tilapia aurea; golden mbuna; Melanochromis auratus (Boulenger, 1897)
Rank
species
Lineage
Show more ... ypterygia; Ctenosquamata; Acanthomorphata; Euacanthomorphacea; Percomorphaceae; Ovalentaria; Cichlomorphae; Cichliformes; Cichlidae; African cichlids; Pseudocrenilabrinae; Haplochromini; Melanochromis
NCBI Taxonomy ID
is Taxon B an Infraspecies?
No
GENOTYPIC CHANGE
Presumptive Null
Yes
Molecular Type
Aberration Type
Deletion Size
1-10 kb
Molecular Details of the Mutation
deletion covering a total of 5.4kb including exon 2 and parts of the flanking introns 1 and 2
Experimental Evidence
Authors
Kratochwil CF; Urban S; Meyer A
Abstract
The tropical freshwater fish family Cichlidae is famous for its record-breaking rates of speciation and diversity in colors and color patterns. Here, we sequenced the genome of the Lake Malawi cichlid Melanochromis auratus to study the genetic basis of an amelanistic morph of this species that lacks the typical melanic stripes and markings. Genome sequencing of the amelanistic and wild-type morph revealed the loss of the second exon of the known pigmentation gene oculocutaneous albinism II (oca2), also known as p(ink-eyed dilution) gene or melanocyte-specific transporter gene. Additional genotyping confirms the complete association with this recessive Mendelian phenotype. The deletion results in a shorter transcript, lacking an acidic di-leucine domain that is crucial for trafficking of the Oca2 protein to melanosomes. The fact that oca2 is involved in a wide range of amelanistic morphs across vertebrates demonstrates its highly conserved function.

© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
Additional References
RELATED GEPHE
Related Genes
No matches found.
Related Haplotypes
No matches found.
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