Biology subjects

Khayatzadeh, N.

Publications and source records attributed to Khayatzadeh, N..

5 recordsLinked to original sources

bioRxiv2026

A large-effect locus on chromosome 4 underlies circadian feeding rhythmicity in pigs

Circadian feeding rhythmicity reflects the distribution of feed intake across the daily 24-hour cycle. Regular feeding-fasting cycles play an important role in regulating metabolism and maintaining health, but endogenous and environmental factors can disrupt the normal circadian pattern of feed intake. Here, we quantified hourly feed intake in 3,470 Swiss Landrace and 15,181 Swiss Large White pigs using 40.5 million records from automated feeding systems. We used the proportion of days exhibiting a significant feeding rhythm after wavelet analysis to investigate variation in circadian feeding organization. Circadian feeding rhythmicity was influenced by sex and age, with higher rhythmicity observed in females and older animals. Variance components analysis revealed a strong additive genetic contribution and a high heritability (0.53-0.57). Pigs with higher circadian feeding rhythmicity had reduced nocturnal intake, improved feed conversion ratio, and lower day-to-day variability in feed intake, suggesting improved feed efficiency and resilience. Genome-wide association testing of 15.7 and 23.1 million imputed sequence variants identified a QTL on chromosome 4 explaining 5.3% and 2.9% of the phenotypic variance of circadian feeding rhythmicity in Swiss Landrace and Swiss Large White pigs, respectively. The QTL overlaps OPRK1 and NPBWR1, two genes implicated in the regulation of feeding behavior, reward and energy homeostasis. Collectively, our findings establish circadian feeding behavior as a heritable trait in pigs and provide a basis to further investigate the genetic regulation of feeding rhythms in mammals and explore its use in animal breeding programs to improve feed efficiency and resilience.

genetics↗

bioRxiv2025

Genetic analysis of iris pigmentation in Swiss pig breeds identifies a missense KITLG variant as a potential causal factor for pale and heterochromatic irises

BackgroundIris pigmentation is a heritable trait with a complex genetic architecture. While the genetic basis of iris pigmentation has been extensively studied in humans, little is known about iris pigmentation in pigs. Iris pigmentation in pigs varies from different shades of brown or pale irises to heterochromia manifesting either as different colors between both irises (heterochromia iridum) or multiple colors within a single iris (heterochromia iridis). This study investigates the genetics of iris pigmentation variability in the Swiss Landrace and Swiss Large White pig breeds. ResultsIris pigmentation was phenotyped in 837 Swiss Landrace and 328 Swiss Large White pigs of which the majority also had array-derived genotypes. A high prevalence of heterochromia iridum (18.6%) was observed in the Swiss Landrace breed. Heritability estimates for iris pigmentation were high in both breeds (h{superscript 2} = 56.0-57.2%). Iris pigmentation was not genetically correlated with production traits. Genome-wide association analysis identified several loci associated with iris pigmentation, including regions near functional candidate genes such as TYR, ALX4 and DCT. The strongest association was detected near the KITLG gene, which was identified as a candidate gene for iris pigmentation in a previous study on Italian Large White pigs. Fine-mapping identified a highly significantly associated (P=3.8x10-11) missense variant in KITLG (5_94084790_G>A, rs342599807, p.R124K) as a potential causal variant for pale and heterochromatic iris pigmentation in Swiss pigs. ConclusionsOur findings provide new insights into the genetic architecture of iris pigmentation in pigs and indicate that KITLG plays a key role. The identification of a putative causal missense variant offers a foundation for further functional studies aiming to better understand pigmentation traits in pigs.

genomics↗

bioRxiv2025

Integrating three genetic dimensions relating to piglet birth weight: direct and maternal effects on the mean and genetic control of residual variance

Uniformity of production traits is desired for different traits in livestock species, including the uniformity of within-litter birth weights in piglets. Birth weight (BW) in pigs is associated with increased vitality and survival until weaning. However, as uniformity of BW increases, the importance of initial weight decreases as competition between piglets decreases. The aim of this study was to estimate the direct and maternal genetic components of BW, jointly with the maternal genetic component of the residual variance for within-litter BW, and their genetic correlations. We used two distinct datasets of Swiss Large White pigs: 1) the experimental farm dataset and 2) the commercial farms dataset, comprising 43,135 and 23,313 records of individual piglet birth weight, respectively. For statistical analysis, the heteroscedastic (or canalising selection) model was used. This model assumes that both the mean BW and the residual variance are affected by systematic and random effects, with the residual variance being heterogeneous and partially under genetic control. Despite the best fitting model was the most complex one including both genetic effects for the mean trait, the results indicated that direct genetic effects, or correlations with such effects, are negligible. The genetic environmental variance for BW ranged between 0.071 and 0.131 for experimental farm and 0.037 to 0.094. The genetic correlation between the mean BW and its variability was always positive and ranged between 0.149 and 0.307 for the experimental farm and between 0.220 and 0.589 for the commercial farms. It is thus sufficient to model BW and its variability by including only the maternal genetic effect for both traits. In addition, even though moderate genetic correlations exist between the mean and the variance of BW, focusing selection on BW uniformity within litters would be preferable to creating a selection index for both traits simultaneously. ImplicationsMonitoring within-litter birth weight variability is important for efficient piglet production and welfare. Our findings suggest that maternal genetic effects are sufficient to model birth weight and its variability as genetic components of environmental variance. For both traits, direct genetic variance and its correlations with other components are negligible. However, since there are moderate genetic correlations between the mean and variance of birth weight, it is preferable to focus solely on selecting for within-litter birth weight uniformity rather than combining both traits in the selection index. This approach simplifies breeding strategies while maintaining the goal of improving piglets welfare. HighlightsO_LIData on individual piglet birth weight were collected on Swiss farms over 18 years C_LIO_LIHeteroscedastic animal models integrated three dimensions of genetic components C_LIO_LIThe direct genetic effect and its correlations are minimal and irrelevant for selection C_LIO_LIMaternal genetic effects are crucial for birth weight and its variability C_LIO_LISelection for uniformity is preferable to selection for both traits simultaneously C_LI

genetics↗

bioRxiv2024

Genome-Wide Association Testing for Haemorrhagic Bowel Syndrome in a Swiss Large White Pig Population

BackgroundThe porcine haemorrhagic bowel syndrome (HBS) is a multifactorial disease causing fatal gastrointestinal disturbances and sudden death in fattening pigs. HBS is the leading cause of deaths during fattening in Swiss pigs, with unclear etiology. Environmental and management factors are associated with HBS incidence, but recent findings also suggest a potential genetic predisposition. Pigs sired by a Swiss Large White (SLW) line appear more prone to HBS. Here we conduct genome-wide association studies (GWAS) for HBS between cases and controls to investigate potential genetic factors for the disease in Swiss fattening pigs. ResultsOur study included 1,036 HBS cases and 4,080 controls with available microarray genotypes or whole-genome sequencing data. Variant positions were determined according to the current porcine reference assembly (Sscrofa11.1) or a HiFi-based SLW haplotype assembly which we constructed using trio-binning. GWAS for HBS were conducted using 12.49 to 15.46 million biallelic variants in three mapping cohorts consisting of purebred animals from SLW sire and dam lines, or crosses between these two parental lines. The statistical model applied for the GWAS accounted for animal relatedness, population structure, and an imbalanced case/control ratio. No sequence variants significantly associated with HBS were identified, regardless of the cohort analysed and the reference sequence considered. ConclusionsThe lack of genetic associations despite a relatively large sample size suggests that susceptibility to HBS in the studied SLW population is not due to large effect variants but may be influenced by numerous small effect genetic variants, in addition to environmental and management factors.

genomics↗

bioRxiv2020

Phylogeny and distribution of Y-chromosomal haplotypes in domestic, ancient and wild goats

The male-specific part of the Y-chromosome is in mammalian and many other species the longest haplotype that is inherited without recombination. By its paternal transmission it has a small effective population size in species with dominant males. In several species, Y-chromosomal haplotypes are sensitive markers of population history and introgression. Previous studies have identified in domestic goats four major Y-chromosomal haplotypes Y1A, Y1B, Y2A and Y2B with a marked geographic differentiation and several regional variants. In this study we used published whole-genome sequences of 70 male goats from 16 modern breeds, 11 ancient-DNA samples and 29 samples from seven wild goat species. We identified single-copy male-specific SNPs in four scaffolds, containing SRY, ZFY, DBY with SSX3Y and UTY, and USP9Y with UMN2001, respectively. Phylogenetic analyses indicated haplogroups corresponding to the haplotypes Y1B, Y2A and Y2B, respectively, but Y1A was split into Y1AA and Y1AB. All haplogroups were detected in ancient DNA samples from southeast Europe and, with the exception of Y1AB, in the bezoar goat, which is the wild ancestor of the domestic goats. Combining these data with those of previous studies and with genotypes obtained by Sanger sequencing or the KASP assay yielded haplogroup distributions for 132 domestic breeds or populations. The phylogeographic differentiation indicated paternal population bottlenecks on all three continents. This possibly occurred during the Neolithic introductions of domestic goats to those continents with a particularly strong influence in Europe along the Danubian route. This study illustrates the power of the Y-chromosomal haplotype for the reconstructing the history of mammalian species with a wide geographic range.

genetics↗