Whole-Genome Resequencing−Based Qualitative Trait Locus Mapping Correlated Iyellow/I with the Mutant Color in Honeybees, IApis cerana cerana/I

This study examined the genetic basis of a mutation in cuticle color in the honeybee Apis cerana cerana using genome resequencing of wild−type and mutant drones produced by a single virgin queen. A candidate locus was identified by calculating the Euclidean distance between mutants and wild types at...

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Veröffentlicht in:Animals (Basel) 2024-03, Vol.14 (6)
Hauptverfasser: Shao, Shanshan, Huang, Qiang, Pei, Yalin, Hu, Junyan, Wang, Zilong, Zhang, Lizhen, He, Xujiang, Wu, Xiaobo, Yan, Weiyu
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container_issue 6
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container_title Animals (Basel)
container_volume 14
creator Shao, Shanshan
Huang, Qiang
Pei, Yalin
Hu, Junyan
Wang, Zilong
Zhang, Lizhen
He, Xujiang
Wu, Xiaobo
Yan, Weiyu
description This study examined the genetic basis of a mutation in cuticle color in the honeybee Apis cerana cerana using genome resequencing of wild−type and mutant drones produced by a single virgin queen. A candidate locus was identified by calculating the Euclidean distance between mutants and wild types at each SNP, performing Lowess regression to fit a curve to these data, and setting a threshold of the top 0.5% Euclidean distance for candidate region selection. From this, genes with synonymous substitutions became candidate genes. One of these genes, the yellow gene, had a 2 bp deletion causing a frameshift mutation. RT−qPCR of this gene was performed on RNA extracted from mutant and wild−type drones; gene expression was only significantly different between wild types and mutants at the yellow gene. Finally, RNA interference silencing of the yellow gene was used to reduce yellow gene expression in workers and putatively result in a lighter coloration. These results indicate that the yellow gene participated in the body pigmentation, and its defect was responsible for the brown mutation. It promotes the understanding of the molecular basis of body coloration in honeybees, enriching the molecular mechanisms underlying insect pigmentation. The honeybee, Apis cerana cerana (Ac), is an important pollinator and has adapted to the local ecological environment with relevant coloration. The cuticle coloration of the brown (br) mutant is brown instead of black in wild−type individuals. Therefore, this study aimed to identify and characterize the gene responsible for the br mutation. Genome resequencing with allele segregation measurement using Euclidean distance followed by Lowess regression analysis revealed that the color locus linked to the mutation was located on chromosome 11. A 2−base deletion on exon 4 was identified in the g7628 (yellow) gene after genome assembly and sequence cloning. In addition, the cuticle color of the abdomen of worker bees changed from black to brown when a defect was induced in the yellow gene using short interfering RNA (siRNA); however, the survival rate did not decrease significantly. These results indicate that the yellow gene participated in the body pigmentation, and its defect was responsible for the br mutation. This study promotes the understanding of the molecular basis of body coloration in honeybees, enriching the molecular mechanisms underlying insect pigmentation.
doi_str_mv 10.3390/ani14060862
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A candidate locus was identified by calculating the Euclidean distance between mutants and wild types at each SNP, performing Lowess regression to fit a curve to these data, and setting a threshold of the top 0.5% Euclidean distance for candidate region selection. From this, genes with synonymous substitutions became candidate genes. One of these genes, the yellow gene, had a 2 bp deletion causing a frameshift mutation. RT−qPCR of this gene was performed on RNA extracted from mutant and wild−type drones; gene expression was only significantly different between wild types and mutants at the yellow gene. Finally, RNA interference silencing of the yellow gene was used to reduce yellow gene expression in workers and putatively result in a lighter coloration. These results indicate that the yellow gene participated in the body pigmentation, and its defect was responsible for the brown mutation. It promotes the understanding of the molecular basis of body coloration in honeybees, enriching the molecular mechanisms underlying insect pigmentation. The honeybee, Apis cerana cerana (Ac), is an important pollinator and has adapted to the local ecological environment with relevant coloration. The cuticle coloration of the brown (br) mutant is brown instead of black in wild−type individuals. Therefore, this study aimed to identify and characterize the gene responsible for the br mutation. Genome resequencing with allele segregation measurement using Euclidean distance followed by Lowess regression analysis revealed that the color locus linked to the mutation was located on chromosome 11. A 2−base deletion on exon 4 was identified in the g7628 (yellow) gene after genome assembly and sequence cloning. In addition, the cuticle color of the abdomen of worker bees changed from black to brown when a defect was induced in the yellow gene using short interfering RNA (siRNA); however, the survival rate did not decrease significantly. These results indicate that the yellow gene participated in the body pigmentation, and its defect was responsible for the br mutation. 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A candidate locus was identified by calculating the Euclidean distance between mutants and wild types at each SNP, performing Lowess regression to fit a curve to these data, and setting a threshold of the top 0.5% Euclidean distance for candidate region selection. From this, genes with synonymous substitutions became candidate genes. One of these genes, the yellow gene, had a 2 bp deletion causing a frameshift mutation. RT−qPCR of this gene was performed on RNA extracted from mutant and wild−type drones; gene expression was only significantly different between wild types and mutants at the yellow gene. Finally, RNA interference silencing of the yellow gene was used to reduce yellow gene expression in workers and putatively result in a lighter coloration. These results indicate that the yellow gene participated in the body pigmentation, and its defect was responsible for the brown mutation. It promotes the understanding of the molecular basis of body coloration in honeybees, enriching the molecular mechanisms underlying insect pigmentation. The honeybee, Apis cerana cerana (Ac), is an important pollinator and has adapted to the local ecological environment with relevant coloration. The cuticle coloration of the brown (br) mutant is brown instead of black in wild−type individuals. Therefore, this study aimed to identify and characterize the gene responsible for the br mutation. Genome resequencing with allele segregation measurement using Euclidean distance followed by Lowess regression analysis revealed that the color locus linked to the mutation was located on chromosome 11. A 2−base deletion on exon 4 was identified in the g7628 (yellow) gene after genome assembly and sequence cloning. In addition, the cuticle color of the abdomen of worker bees changed from black to brown when a defect was induced in the yellow gene using short interfering RNA (siRNA); however, the survival rate did not decrease significantly. These results indicate that the yellow gene participated in the body pigmentation, and its defect was responsible for the br mutation. 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A candidate locus was identified by calculating the Euclidean distance between mutants and wild types at each SNP, performing Lowess regression to fit a curve to these data, and setting a threshold of the top 0.5% Euclidean distance for candidate region selection. From this, genes with synonymous substitutions became candidate genes. One of these genes, the yellow gene, had a 2 bp deletion causing a frameshift mutation. RT−qPCR of this gene was performed on RNA extracted from mutant and wild−type drones; gene expression was only significantly different between wild types and mutants at the yellow gene. Finally, RNA interference silencing of the yellow gene was used to reduce yellow gene expression in workers and putatively result in a lighter coloration. These results indicate that the yellow gene participated in the body pigmentation, and its defect was responsible for the brown mutation. It promotes the understanding of the molecular basis of body coloration in honeybees, enriching the molecular mechanisms underlying insect pigmentation. The honeybee, Apis cerana cerana (Ac), is an important pollinator and has adapted to the local ecological environment with relevant coloration. The cuticle coloration of the brown (br) mutant is brown instead of black in wild−type individuals. Therefore, this study aimed to identify and characterize the gene responsible for the br mutation. Genome resequencing with allele segregation measurement using Euclidean distance followed by Lowess regression analysis revealed that the color locus linked to the mutation was located on chromosome 11. A 2−base deletion on exon 4 was identified in the g7628 (yellow) gene after genome assembly and sequence cloning. In addition, the cuticle color of the abdomen of worker bees changed from black to brown when a defect was induced in the yellow gene using short interfering RNA (siRNA); however, the survival rate did not decrease significantly. These results indicate that the yellow gene participated in the body pigmentation, and its defect was responsible for the br mutation. This study promotes the understanding of the molecular basis of body coloration in honeybees, enriching the molecular mechanisms underlying insect pigmentation.</abstract><pub>MDPI AG</pub><doi>10.3390/ani14060862</doi></addata></record>
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subjects Analysis
Bees
Gene expression
Genetic aspects
Genomes
Genomics
Honeybee
RNA
title Whole-Genome Resequencing−Based Qualitative Trait Locus Mapping Correlated Iyellow/I with the Mutant Color in Honeybees, IApis cerana cerana/I
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