Abstract

Single nucleotide polymorphisms (SNPs) located in transcript sequences showing allele-specific expression (ASE SNPs) were previously identified in the Longissimus thoracis muscle of a Nelore (Bos indicus) population consisting of 190 steers. Given that the allele-specific expression pattern may result from cis-regulatory SNPs, called allele-specific expression quantitative trait loci (aseQTLs), in this study, we searched for aseQTLs in a window of 1 Mb upstream and downstream from each ASE SNP. After this initial analysis, aiming to investigate variants with a potential regulatory role, we further screened our aseQTL data for sequence similarity with transcription factor binding sites and microRNA (miRNA) binding sites. These aseQTLs were overlapped with methylation data from reduced representation bisulfite sequencing (RRBS) obtained from 12 animals of the same population. We identified 1134 aseQTLs associated with 126 different ASE SNPs. For 215 aseQTLs, one allele potentially affected the affinity of a muscle-expressed transcription factor to its binding site. 162 aseQTLs were predicted to affect 149 miRNA binding sites, from which 114 miRNAs were expressed in muscle. Also, 16 aseQTLs were methylated in our population. Integration of aseQTL with GWAS data revealed enrichment for traits such as meat tenderness, ribeye area, and intramuscular fat . To our knowledge, this is the first report of aseQTLs identification in bovine muscle. Our findings indicate that various cis-regulatory and epigenetic mechanisms can affect multiple variants to modulate the allelic expression. Some of the potential regulatory variants described here were associated with the expression pattern of genes related to interesting phenotypes for livestock. Thus, these variants might be useful for the comprehension of the genetic control of these phenotypes.

Highlights

  • Single nucleotide polymorphisms (SNPs) located in transcript sequences showing allele-specific expression (ASE single nucleotide polymorphisms (SNP)) were previously identified in the Longissimus thoracis muscle of a Nelore (Bos indicus) population consisting of 190 steers

  • We identified 1134 aseQTLs associated with the Allele-specific expression (ASE) pattern of 126 SNPs in the Longissimus thoracis muscle of Nelore steers

  • Thirty-seven ASE SNPs associated with aseQTLs were described in a previous ASE study developed with bovine muscle ­samples[8]

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Summary

Introduction

Single nucleotide polymorphisms (SNPs) located in transcript sequences showing allele-specific expression (ASE SNPs) were previously identified in the Longissimus thoracis muscle of a Nelore (Bos indicus) population consisting of 190 steers. Given that the allele-specific expression pattern may result from cis-regulatory SNPs, called allele-specific expression quantitative trait loci (aseQTLs), in this study, we searched for aseQTLs in a window of 1 Mb upstream and downstream from each ASE SNP After this initial analysis, aiming to investigate variants with a potential regulatory role, we further screened our aseQTL data for sequence similarity with transcription factor binding sites and microRNA (miRNA) binding sites. De Souza et al.[5] identified SNPs in transcribed regions showing allele-specific expression patterns (ASE SNPs) in the muscle of Nelore (Bos indicus) related to meat tenderness, an important trait for meat consumer’s ­approval[6,7] Many of these SNPs were located within genes responsible for essential biological functions for muscle development and meat t­enderness[5]. In a heterozygous locus, if the regulatory region of only one allele has an affinity with the transcription factor (TF), this cis-regulatory variant can lead to A­ SE16

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