| Literature DB >> 32615043 |
Sayed Haidar Abbas Raza1, Li Shijun1, Rajwali Khan1, Nicola M Schreurs2, Zeinab Manzari3, Ayman Hassan Abd El-Aziz4, Irfan Ullah5, Nurgulsim Kaster1, Mujahid Ali Shah6, Linsen Zan1,7.
Abstract
The PLIN1 gene produces a phosphorylated protein wrapped in lipid droplets in adipocytes. This phosphorylation assists the mobilization of fat into adipose tissue. The purpose of the experiment was to study the polymorphism of the PLIN1 gene and its relationship with the body and carcass characteristics of Qinchuan cattle to find molecular genetic markers that can be used for breeding. The expression level of the PLIN1 gene was determined in various tissues by qRT-PCR. The results showed that the highest level of PLN1 expression was found in subcutaneous fat, followed by the heart and longissimus muscle, and the lowest level was found in the kidney. Five SNP loci of the PLIN1 gene were identified in 510 Qinchuan cattle, including g.3580T>C (SNP1), g.3898G>A (SNP2), g.8333G>A (SNP3), g.10517T>C (SNP4), and g.10538G>T (SNP5). The results show that SNP1, SNP2, SNP3, and SNP4 were moderately polymorphic (0.25 < PIC < 0.5), while SNP5 was minimally polymorphic (PIC < 0.25). SNP2, SNP3, and SNP5 were within Hardy-Weinberg equilibrium (P > 0.05), but SNP1 and SNP4 were not (P < 0.05). Correlation analysis showed that the five SNPs of the PLIN1 gene were correlated with back-fat depth, intramuscular fat, and chest depth of Qinchuan cattle. The double haplotype H2H4 in Qinchuan beef was associated with body and carcass traits. We conclude that variants mapped within PLIN1 can be used in marker-assisted selection for carcass quality and body traits in breed improvement programs for Qinchuan cattle.Entities:
Keywords: PLIN1 gene; Qinchuan cattle; body measurement traits; bovins Qinchuan; caractères de la morphologie corporelle; expression de l’ARNm; gène PLIN1; mRNA expression; marker-assisted selection; polymorphismes mononucléotidiques; single nucleotide polymorphisms; sélection assistée par marqueurs
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Year: 2020 PMID: 32615043 DOI: 10.1139/gen-2019-0184
Source DB: PubMed Journal: Genome ISSN: 0831-2796 Impact factor: 2.166