Article Abstract

Volume 25, No. (6), 2015 (December)
PRLR, MC4R AND LEP POLYMORPHISMS, AND ADIPOQ, A-FABP AND LEP EXPRESSION IN CROSSBRED MANGALICA PIGS
Tempfli, Károly, Simon, Zoltán, Kovács, Bálint, Posgay, Miklós, and Bali Papp, Ágnes

Tempfli, Károly, Simon, Zoltán, Kovács, Bálint, Posgay, Miklós, and Bali Papp, Ágnes

1University of West Hungary, Faculty of Agricultural and Food Sciences, Institute of Animal Sciences, 4 Vár st., 9200 Mosonmagyaróvár, Hungary
2Olmos and Tóth Ltd., 6 Hatvan st., 4025 Debrecen, Hungary

Corresponding Author: tempflik@gmail.com
DOI: NA
Page Number(s): 1746-1752
Published Online First: December 01, 2015
Publication Date: December 01, 2015
ABSTRACT

Mangalica×Duroc crossbred pigs were genotyped for the G1789prolactin receptor (PRLR), G1426melanocortin-4 receptor (MC4R), and T3469leptin (LEP) single nucleotide polymorphisms (SNPs) by means of the PCR-RFLP method; genotype-trait associations were also analysed. The PRLR genotype did not influence (P>0.05) any production traits monitored, whereas the MC4R genotype significantly (P<0.05) affected backfat thickness and average daily gain during the fattening period. The LEP genotype was also significantly (P<0.05) associated with average daily gain. In crossbred gilts the expression of the adiponectin (ADIPOQ), adipocyte fatty acid-binding protein (A-FABP), and LEP genes was analysed in adipose and muscle tissues using qRT-PCR. ADIPOQ was predominantly expressed in backfat (P<0.05); however, mRNA was also detected in muscle samples indicating high intramuscular fat content. The A-FABP and LEP genes were more active in fat tissue with moderately lower levels also in muscle, contributing to intramuscular fat accumulation. MC4R and LEP polymorphisms are promising markers for production traits in the crossbred animals, whereas ADIPOQ expression is suggested as a potential indicator of elevated intramuscular fat content.

Keywords: gene expression; polymorphism; backfat thickness, Mangalica pig
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JCR Year: 2025

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Print ISSN: 1018-7081

Electronic ISSN: 2309-8694

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