Genomic Basis of Striking Fin Shapes and Colors in the Fighting Fish

Abstract Resolving the genomic basis underlying phenotypic variations is a question of great importance in evolutionary biology. However, understanding how genotypes determine the phenotypes is still challenging. Centuries of artificial selective breeding for beauty and aggression resulted in a plet...

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Bibliographic Details
Published in:Molecular biology and evolution 2021-08, Vol.38 (8), p.3383-3396
Main Authors: Wang, Le, Sun, Fei, Wan, Zi Yi, Ye, Baoqing, Wen, Yanfei, Liu, Huiming, Yang, Zituo, Pang, Hongyan, Meng, Zining, Fan, Bin, Alfiko, Yuzer, Shen, Yubang, Bai, Bin, Lee, May Shu Qing, Piferrer, Francesc, Schartl, Manfred, Meyer, Axel, Yue, Gen Hua
Format: Article
Language:English
Subjects:
Analysis
Animal behavior
Animal Fins - anatomy & histology
Animals
Discoveries
Domestication
Evolutionary biology
Female
Fishes
Genetic aspects
Genetic Variation
Genome
Genomes
Genomics
Male
Perciformes - anatomy & histology
Perciformes - genetics
Phenotype
Pigmentation - genetics
Potassium channels
Quantitative genetics
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Summary:Abstract Resolving the genomic basis underlying phenotypic variations is a question of great importance in evolutionary biology. However, understanding how genotypes determine the phenotypes is still challenging. Centuries of artificial selective breeding for beauty and aggression resulted in a plethora of colors, long-fin varieties, and hyper-aggressive behavior in the air-breathing Siamese fighting fish (Betta splendens), supplying an excellent system for studying the genomic basis of phenotypic variations. Combining whole-genome sequencing, quantitative trait loci mapping, genome-wide association studies, and genome editing, we investigated the genomic basis of huge morphological variation in fins and striking differences in coloration in the fighting fish. Results revealed that the double tail, elephant ear, albino, and fin spot mutants each were determined by single major-effect loci. The elephant ear phenotype was likely related to differential expression of a potassium ion channel gene, kcnh8. The albinotic phenotype was likely linked to a cis-regulatory element acting on the mitfa gene and the double-tail mutant was suggested to be caused by a deletion in a zic1/zic4 coenhancer. Our data highlight that major loci and cis-regulatory elements play important roles in bringing about phenotypic innovations and establish Bettas as new powerful model to study the genomic basis of evolved changes.
ISSN:1537-1719
0737-4038
1537-1719
DOI:10.1093/molbev/msab110