Verification of Key Target Molecules for Intramuscular Fat Deposition and Screening of SNP Sites in Sheep from Small-Tail Han Sheep Breed and Its Cross with Suffolk

Author:

Fu Lingjuan1,Shi Jinping1,Meng Quanlu1,Tang Zhixiong1,Liu Ting1,Zhang Quanwei2ORCID,Cheng Shuru1

Affiliation:

1. College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China

2. College of Life Science and Technology, Gansu Agricultural University, Lanzhou 730070, China

Abstract

Intramuscular fat (IMF) is vital for meat tenderness and juiciness. This study aims to explore the IMF deposition mechanism and the related molecular markers in sheep. Two populations, Small-tail Han Sheep (STH) and STH × Suffolk (SFK) F1 (SFK × STH), were used as the research object. Histological staining techniques compared the differences in the longissimus dorsi muscle among populations. A combination of transcriptome sequencing and biological information analysis screened and identified IMF-related target genes. Further, sequencing technology was employed to detect SNP loci of target genes to evaluate their potential as genetic markers. Histological staining revealed that the muscle fiber gap in the SFK × STH F1 was larger and the IMF content was higher. Transcriptome analysis revealed that PIK3R1 and PPARA were candidate genes. Histological experiments revealed that the expressions of PIK3R1 mRNA and PPARA mRNA were lower in SFK × STH F1 compared with the STH. Meanwhile, PIK3R1 and PPARA proteins were located in intramuscular adipocytes and co-located with the lipid metabolism marker molecule (FASN). SNP locus analysis revealed a mutation site in exon 7 of the PIK3R1 gene, which served as a potential genetic marker for IMF deposition. This study’s findings will provide a new direction for meat quality breeding in sheep.

Funder

Gansu Provincial Department of Science and Technology’s Technical Innovation Guidance Plan—Rural Revitalization Special Project

Gansu Agricultural University Discipline Team Project

Publisher

MDPI AG

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