Effect of single nucleotide polymorphisms on intramuscular fat content in Hungarian Simmental cattle.
The main aim of modern livestock agriculture is to satisfy the growing demands of consumers for high-quality, safe and delicious animal products. This trend is evident for the beef industry as well. The proper breeding scheme in the past was very successful in increasing of lean meat content, but resulted in reduced intramuscular fat content (IMF) and changed muscle fibre types as well . Nowadays, the main aim of numerous studies is improvement of IMF in beef  and investigation of relationship between beef quality and muscle biochemical characteristics such as connective tissue and muscle fibres . The Association of Hungarian Simmental Cattle Breeders has been taking measures in the last years to improve beef quality. For breeding purpose and market expectations, it was developed a new dual purpose index where weighting of breeding values is quoted as follows: 40% for milk, 30% for meat and 30% for fitness . At present, there is considerable interest in the application of genomic breeding value estimation to promote rapid and efficient selection in farm animals. Some single nucleotide polymorphisms (SNPs) have been demonstrated to affect IMF and meat quality traits in farm animals [5, 6]. Genome-wide association study (GWAS) based on typing of 777,000 SNPs by DNA chip technique is suitable for the improvement of beef quality and IMF in different cattle breeds. Availability of genomic information on a large number of animals has changed the dairy cattle breeding worldwide . In case of beef cattle [8, 9] and dual purpose cattle, result of GWAS can also change the selection progress, though the effective population number and the accuracy of estimated genomic breeding value is lower compared to dairy cattle. Aim of present investigation was to estimate the effect of SNP polymorphisms on IMF.
MATERIALS AND METHODS
A total of 146 Hungarian Simmental muscle samples from eleven farms were collected and were stored in liquid nitrogen at -196[degrees]C until DNA extraction. Animals were kept in identical conditions, fed the same diet and slaughtered at approximately similar live weight (530.6 [+ or -] 44.7 kg), under commercial conditions using Hungarian standard procedure.
During slaughtering, rib samples have been taken from longissimus dorsi muscle (LD) cut between the 11th to 13th rib. Chemical percentage IMF was determined from LD. After removing surface fat, lipid content of LD was determined gravimetrically by Soxhlet method, using petroleum ether as solvent . Lipid content (IMF values) ranged from 0.5% to 5.8%.
For isolation of genomic DNA from muscle, samples were incubated in 5% Chelex suspension and 0.6 [micro]g/[micro]L Proteinase-K solution at 56[degrees]C, overnight. Final treatment of the mixture was an incubating step at 98[degrees]C for ten minutes. After DNA extraction from LD, SNP typing was performed with high-resolution SNP chips developed for cattle (Illumina Bovine HD Chip, San Diego, CA, USA). Illumina Final Report file was imported into SVS software (GoldenHelix, Bozeman, MT, USA). Samples were excluded from analysis if call rate was below 95%. Only SNPs having consistently high call rate (>95%) were included in this study. Duplicated samples (IBD >0.95) were excluded from dataset. After excluding monomorphic loci and loci with minor allele frequency <0.05, dataset included 129 animals and 120,774 SNPs. Statistical analyses were performed by SVS software (GoldenHelix, USA). For visualising results, high resolution image has been produced by R using qqman library .
For correction of population structure, genomic kinship matrix has been used in multi-locus mixed-model . Phenotypic values have been left as they were, a continuous variable.
The used model was
y = X[beta]+Zu+e
Where y is the IMF, X is the matrix of fixed effects composed of SNPs and covariates (age and sex), Z is the matrix of random animal effects. The e means the residual effects. The [beta] and u are vectors representing coefficients of fixed and random effects, respectively.
The Ensemble cow UMD3.1 and gene ontology (GO)  databases were used to look for surrounding of most significant SNPs and for functional categories.
RESULTS AND DISCUSSION
Four loci have been identified to be highly associated with IMF (Figure 1). These loci (-[log.sub.10]P>12) seem to be useful in selection programs and are located on chromosome 1, 6, 13, and 17, their minor allele frequencies are 0.426, 0.221, 0.162, and 0.106, respectively (Table 1). IMF values--extracted from the database consisting of recorded values for different metabolites and for carcass parts--ranged from 0.5% to 5.8%.
On chromosome 1 there are several protein coding sequences in near vicinity of the locus rs43284251, including polypeptide N-acetylgalactosaminyltransferase 15 (GALNT15), diphthamide biosynthesis 3 (DPH3), and serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit A (ANKRD28).
GALNT15 (GO:0030133, 0000139, 0016021, 0006486, 0030246, 0016757)--also known as GALNTL2, pp-GalNAcT15, or GALNT7--is part of glycoproteome playing role in cell interactions with environment . GALNTs are localised in Golgi and endoplasmatic reticulum (ER). Their traffic from Golgi to ER often activated in human malignant tumors. In human, nonhuman primates and rodents, loss of function of GALNT2 has been shown to lower high-density lipoproteins and species specific glycosylation targets has been identified . An allele of GALNT13 in human has been found to be overrepresented in elite sprinters  suggesting involvement in energy pathways. Functions of GALNTs are not fully understood, but their targets [17,18] may affect lipoprotein metabolism and fat deposition in intramuscular space.
DPH3 (GO:0046872, 0017183, 0051099, 0050709, 0005829, 0005654) is essential in the synthesis of diphtamide posttranslationally modificate histidine elongation factor 2 . Down-regulation increases extracellular release of proteoglycans, indicating a possible role in the secretion process.
ANKRD28 is related to pathways (http://pathcards.genecards.org/) like Vesicle-mediated transport and Transport to the Golgi and subsequent modification.
On chromosome 6 there are several protein coding sequences in near vicinity of the locus rs109210955, including leucine aminopeptidase (LAP3), mediator of RNA polymerase II transcription subunit 28 (MED28), family with sequence similarity 184 member B (FAM184B), DDB1 and CUL4 associated factor 16 (DCAF16), non-SMC condensin I complex subunit G (NCAPG), ligand-dependent nuclear receptor corepressor-like protein (LCORL). Haplotypes of LAP3 (GO: 0008235, 0004177, 0030145, 0008233, 0097718, 0006508, 0070062, 0005925, 0005737, 0005739, 0005829, 0030496, 0005654) gene is reported  to be used as molecular marker in association with milk production and other performance related traits. MED28 (GO:0019827, 0051151, 0016592, 0030864) has negative regulation effect on smooth muscle cell differentiation. In vivo fate mapping showed, that a set of adipocytes arose from smooth muscle-like origin . DCAF16 (GO:0016567, 0080008) is associated with average daily gain in cattle .
NCAPG (GO: 0007076, 0000793, 0005737, 0000779, 0000796) is a major player in cellular maintenance processes and a major contributor to genetic variability in bovine feed efficiency . Expression of NCAPG together with LCORL (GO:0003677, 0006366, 0006357) measured in adipose and muscle tissue are associated with cattle feed intake and weight gain . NCAPG affects arginine metabolism having influence on body-mass gain and lipid deposition.
Locus rs41630030 on Chr 13 is located close to ADP-ribosylation factor-related protein 1 (ARFRP1), TNF receptor superfamily member 6b (TNFRSF6B ENSBTAG00000027407). ARFRP1 (GO:0005525, 0007264, 0034067, 0043001, 0042147, 0007369, 0005802, 0016020, 0005829) is required for the lipidation of chylomicrons in the intestine and required for very low density lipoprotein (VLDL) lipidation in the liver , TNFRSF6B might have role in response to lipopolysaccharide according to one of the GO annotations (GO:0032496). Its expression has been detected in bovine ovarian follicles . There are also two transcripts overlapping rs41630030; ENSBTAT00000045108. 3 (GO:0005524, 0004003, 0032508) and ENSBTAT00000052120.2. (GO:0003677, 0005524, 0004003, 0032508, 0006139, 0005634). GO annotation number 0006139 suggests this transcript is involved in nucleobase-containing compound metabolic process.
Nearby locus rs41642251 on Chr 17 preferentially expressed antigen in melanoma (PRAME) and splicesomal RNA (U1) loci are located. PRAME (GO:0045892, 0045596, 0043066, 0008284) were shown that lipopolysaccharide together with type 2 interferon has increased its expression . Literature on U1 was not available, however lack of activity of splicing factor SRSF10 affected development of adipose tissue  in cell culture. Contribution of different splicing events to the adipose tissue thermogenesis is involved in development of diet-induced obesity in mice .
Fatty acid binding protein 4 (FABP4) alleles in Japanese Black  and in Holstein cattle  have effect on IMF, whereas in Korean cattle  it affects backfat thickness. In Fleckvieh cattle  looked for genomic regions showing associations with IMF, analysing diacylglycerol o-acyltransferase 1 (DGAT1), FABP4, fatty acid synthase (FASN) and peroxisome proliferator activated receptor gamma coactivator 1 alpha (PPARGC1A) genes on chromosome 14, 14, 19, and 6, respectively. In our study, none of them was significantly associated with IMF content. However in previous studies we demonstrated the effect of leptin (Chr 4), DGAT1 (Chr 14) and thyroglobulin (Chr 14) gene polymorphisms on the IMF of Angus cattle .
The IMF or marbling represents a valuable beef quality trait and is important determinant of palatability due to its contribution to juiciness and flavour. Meat with low IMF may be dry and flavourless. Higher levels of IMF have been associated with increased tenderness, juiciness and flavour of beef [35,36]. Molecular tests can provide facilities for direct selection among variants. However, benefits of different alleles depend on economic reasons given in the breeding programs. Herewith we propose to follow up segregation of alleles of the found loci in the Simmental population, and to continue phenotypic characterisations in the upcoming generations. After successful validation, selection for favourable alleles at reported loci on chromosomes mentioned above (Chr 1, 6, 13, and 17) could be utilised, if increased IMF is desirable.
CONFLICT OF INTEREST
We certify that there is no conflict of interest with any financial organization regarding the material discussed in the manuscript.
This project was supported by the Hungarian Scientific Research Fund (Project 111643).
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Istvan Anton (1), Balazs Huth (2, 3), Imre Fuller (3), Laszlo Rozsa (1), Gabriella Hollo (2), and Attila Zsolnai (1, 2) *
* Corresponding Author: Attila Zsolnai Tel: +36-23-319-133, Fax: +36-23-319-133(120), E-mail: firstname.lastname@example.org
(1) NARIC-Research Institute for Animal Breeding Nutrition and Meat Science, Gesztenyes u. 1., Herceghalom, 2053, Hungary
(2) Department of Animal Husbandry and Management, Institute of Animal Science, Faculty of Agricultural and Environmental Sciences, University of Kaposvar, Kaposvar, Guba S. u. 40., 7400, Hungary
(3) Association of Hungarian Simmental Cattle Breeders, Zrinyi u. 3., Bonyhad, 7150, Hungary
Submitted Oct 19, 2017; Revised Dec 19, 2017; Accepted Mar 12, 2018
Caption: Figure 1. Manhattan plot of single nucleotide polymorphisms regarding intramuscular fat content (IMF). Loci on chromosome 1, 6, 13, and 17 display the highest -[log.sub.10]P values (see dots >12), which are associated with the intramuscular fat content in Hungarian Simmental cattle.
Table 1. List of loci associated with intramuscular fat content (IMF), their genomic location and nearest genes Marker ss ID (variant Chr Position -[log.sub.10]P type) rs43284251 intergenic 1 154894091 12.2 rs109210955 intergenic 6 39358026 16.3 rs41630030 intronic 13 54540476 15.5 rs41642251 intergenic 17 26689850 21.7 Marker ss ID (variant -[log.sub.10]P Nearest genes type) after Bonferroni (their distance from correction the marker in bp) rs43284251 intergenic 7.1 GALNT15 (29068), DPH3 (110416), ANKRD28 -325755 rs109210955 intergenic 11.2 LAP3 (757999), MED28 (749185), FAM184B (685720), DCAF16 (603129), NCAPG (545975), LCORL (365914) rs41630030 intronic 10.4 ARFRP1 (14722), TNFRSF6B (12525), ENSBTAT00000045108, ENSBTAT00000052120 rs41642251 intergenic 16.7 PRAME (1567997), U1 (251068), Marker ss ID (variant MAF FDR type) rs43284251 intergenic 0.426 2.6e-8 rs109210955 intergenic 0.221 2.4e-12 rs41630030 intronic 0.162 1.3e-11 rs41642251 intergenic 0.106 2.6e-17 MAF, minor allele frequency; FDR, false discovery rate; GALNT15, polypeptide N-acetylgalactosaminyltransferase 15; LAP3, leucine aminopeptidase; MED28, mediator of RNA polymerase II transcription subunit 28; FAM184B, family with sequence similarity 184 member B; DCAF16, DDB1 and CUL4 associated factor 16; NCAPG, non-SMC condensin I complex subunit G; LCORL, ligand-dependent nuclear receptor corepressor-like protein; ARFRP1, ADP-ribosylation factor-related protein 1; TNFRSF6B, TNF receptor super-family member 6b; PRAME, preferentially expressed antigen in melanoma; U1, splicesomal RNA.
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|Author:||Anton, Istvan; Huth, Balazs; Fuller, Imre; Rozsa, Laszlo; Hollo, Gabriella; Zsolnai, Attila|
|Publication:||Asian - Australasian Journal of Animal Sciences|
|Date:||Sep 1, 2018|
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