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. 2021 Aug 11:12:698163.
doi: 10.3389/fgene.2021.698163. eCollection 2021.

A Missense Mutation in the MYBPH Gene Is Associated With Abdominal Fat Traits in Meat-Type Chickens

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A Missense Mutation in the MYBPH Gene Is Associated With Abdominal Fat Traits in Meat-Type Chickens

Priscila Anchieta Trevisoli et al. Front Genet. .

Abstract

Chicken is an important source of protein for human nutrition and a model system for growth and developmental biology. Although the genetic architecture of quantitative traits in meat-type chickens has been the subject of ongoing investigation, the identification of mutations associated with carcass traits of economic interest remains challenging. Therefore, our aim was to identify predicted deleterious mutation, which potentially affects protein function, and test if they were associated with carcass traits in chickens. For that, we performed a genome-wide association analysis (GWAS) for breast, thigh and drumstick traits in meat-type chickens and detected 19 unique quantitative trait loci (QTL). We then used: (1) the identified windows; (2) QTL for abdominal fat detected in a previous study with the same population and (3) previously obtained whole genome sequence data, to identify 18 predicted deleterious single nucleotide polymorphisms (SNPs) in those QTL for further association with breast, thigh, drumstick and abdominal fat traits. Using the additive model, a predicted deleterious SNP c.482C > T (SIFT score of 0.4) was associated (p-value < 0.05) with abdominal fat weight and percentage. This SNP is in the second exon of the MYBPH gene, and its allele frequency deviates from Hardy-Weinberg equilibrium. In conclusion, our study provides evidence that the c.482C > T SNP in the MYBPH gene is a putative causal mutation for fat deposition in meat-type chickens.

Keywords: MYBPH; abdominal fat; chicken; meat-type; predicted deleterious SNPs.

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Conflict of interest statement

FAPESP, CAPES, CNPq, and the Brazilian Government through Embrapa provided financial support to generate the data; however, they did not participate in the design of the study, sample collection, analysis, data interpretation, and writing of the manuscript. The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as apotential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Workflow of genomic analysis performed.

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