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Copy number variations (CNVs) are major forms of genetic variation with an increasing importance in animal genomics. This study used the Illumina BovineSNP 50 K BeadChip to detect the genome-wide CNVs in the Tharparkar cattle. With the aid of PennCNV software, we noticed a total of 447 copy number variation regions (CNVRs) across the autosomal genome, occupying nearly 2.17% of the bovine genome. The average size of detected CNVRs was found to be 122.2 kb, the smallest CNVR being 50.02 kb in size, to the largest being 1,232.87 Kb. Enrichment analyses of the genes in these CNVRs gave significant associations with molecular adaptation-related Gene Ontology (GO) terms. Most CNVR genes were significantly enriched for specific biological functions; signaling pathways, sensory responses to stimuli, and various cellular processes. In addition, QTL analysis of CNVRs described them to be linked with economically essential traits in cattle. The findings here provide crucial information for constructing a more comprehensive CNVR map for the indigenous cattle genome. [ABSTRACT FROM AUTHOR]

Natural fibers derived from diverse animal species have gained increased attention in recent years due to their favorable environmental effects, long‐term sustainability benefits, and remarkable physical and mechanical properties that make them valuable raw materials used for textile and non‐textile production. Domestication and selective breeding for the economically significant fiber traits play an imperative role in shaping the genomes and, thus, positively impact the overall productivity of the various fiber‐producing species. These selection pressures leave unique footprints on the genome due to alteration in the allelic frequencies at specific loci, characterizing selective sweeps. Recent advances in genomics have enabled the discovery of selection signatures across the genome using a variety of methods. The increased demand for 'green products' manufactured from natural fibers necessitates a detailed investigation of the genomes of the various fiber‐producing plant and animal species to identify the candidate genes associated with important fiber attributes such as fiber diameter/fineness, color, length, and strength, among others. The objective of this review is to present a comprehensive overview of the concept of selection signature and selective sweeps, discuss the main methods used for its detection, and address the selection signature studies conducted so far in the diverse fiber‐producing animal species. [ABSTRACT FROM AUTHOR]

Classical Swine Fever (CSF) is a contagious viral disease of pigs which is endemic in several parts of the world, including India. Prophylactic vaccination using live attenuated vaccine is the preferred method of control. However, there is significant inter-individual variation in the antibody response to vaccination. In this study, we measured the E2 antibody blocking percentage after 21 days of CSF vaccination in a mixed pig population consisting of Landrace, indigenous Ghurrah pigs, and their crossbreds. A Genome Wide Association Study (GWAS) carried out using single-SNP and haplotype based methods detected a 1.6 Mb region on SSC2 (28.92−30.52 Mb) as significantly associated with antibody response to CSF vaccination. The significant region and 1 Mb flanking sequences encompass 3 genes – EIF3M, DNAJC24 and ARL14EP, which code for proteins involved in Pestivirus replication and host immune response system. Our results combined with previous studies on immune response of pigs present this region as a suitable candidate for future functional investigations. [ABSTRACT FROM AUTHOR]

The present study was undertaken to identify the microRNAs (miRNAs) expressed in the mammary tissue of a bubaline heifer. Small RNAs were isolated from the mammary gland tissue and enriched for miRNA fraction. The linker-ligated small RNAs were reverse transcribed to synthesize cDNA and amplified by PCR. The PCR products were ligated to the pGEM-T Easy vector; cloned into DH5 alpha cells and sequenced. Sequencing of 40 clones, randomly chosen from this library, produced 115 concatemerized short sequences. The short sequences were checked for their matches with the help of refseq_rna database, EST database (NCBI) and Ensembl. The analysis was performed for more than 90% identity with miRNAs across different species in miRBase. Alignment of putative small RNA sequences with the bovine genome was attempted in GenBank (NCBI) and Ensembl using BLAST. The small RNA sequences with a partial matches within the bovine genome and/or with flanking sequences (upstream or downstream) were analyzed for hairpin structures using the Mfold web server. Reverse complements were also assessed for the homology search. miRNA sequences showing only a partial match with already reported sequences were considered as a putative bubaline miRNAs. Six developmentally important putative miRNA precursors were identified from this study using cloning and sequencing followed by the Bioinformatics approach. This study will help in the elucidation of pathways involving miRNAs in bubaline species at the heifer stage. [ABSTRACT FROM AUTHOR]

Knowledge about genetic diversity is very essential for the management and sustainable utilization of livestock genetic resources. In this study, we presented a comprehensive genome-wide analysis of genetic diversity, ROH, inbreeding, linkage disequilibrium, effective population size and haplotype block structure in Tharparkar cattle of India. A total of 24 Tharparkar animals used in this study were genotyped with Illumina BovineSNP50 array. After quality control, 22,825 biallelic SNPs were retained, which were in HWE, MAF > 0.05 and genotyping rate >90%. The overall mean observed (HO) and expected heterozygosity (HE) were 0.339 ± 0.156 and 0.325 ± 0.129, respectively. The average minor allele frequency was 0.234 with a standard deviation of ± 0.131. We identified a total of 1832 ROH segments and the highest autosomal coverage of 13.87% was observed on chromosome 23. The genomic inbreeding coefficients estimates by FROH, FHOM, FGRM and FUNI were 0.0589, 0.0215, 0.0532 and 0.0160 respectively. The overall mean linkage disequilibrium (LD) for a total of 133,532 pairwise SNPs measured by D' and r2 was 0.6452 and 0.1339, respectively. In addition, we observed a gradual decline in effective population size over the past generations. [ABSTRACT FROM AUTHOR]

The analysis of genetic diversity is very essential to understand the evolution and adaptability of livestock species to different environmental conditions. Genetic variation is the raw material for selection and foundation for breed improvement programmes. The use of high throughput molecular marker technologies, advanced statistical and software tools have revolutionized the precision of animal genetic diversity analysis in a large number of populations with limited time and resources. SNP genotyping is one of the best methods to study genetic variation due to its abundance in livestock species, stability and cost-effectiveness. In this review, some of the most popularly used diversity analysis software programs in livestock genomics are discussed briefly. Microsatellite-based software such as Genepop, Fstat, Genetix, TFPGA, Stackpack, Arlequin and other multipurpose software such as PLINK, PowerMarker, TASSEL, BEAGLE, R software packages (GenABEL, SNPassoc, snpstats, SNP relate), Gemma, SNP Express, SVS, etc. can be utilized for diversity analysis. [ABSTRACT FROM AUTHOR]

Epigenetics refers to the study of heritable phenotypic changes without alterations in the DNA sequence. Advanced studies in epigenetic molecular mechanisms and their biological functions have relied on various model systems including bacteria, fungi, plants, insects, and mammals. The fruit fly Drosophila melanogaster has been an established model organism in the study of genetics and developmental biology. Many regulatory pathways are conserved in Drosophila compared to mammals, rendering it a powerful model to study epigenetic mechanisms. In this review, we outline the various epigenetic mechanisms and their importance in Drosophila chiefly focussing on the predominant epigenetic variations such as DNA methylation, histone modifications like H3K18 acetylation, H3K27 and H4K20 methylation, H3S10 phosphorylation, H2K118 ubiquitylation, H4 sumoylation, RNA associated silencing, polycomb proteins, PEV (position effect variegation), TPE (Telomeric position effect), and dosage compensation. All these types of epigenetic mechanisms can be studied precisely in Drosophila by inducing various mutations in the genome. Advanced studies in Drosophila epigenetics helps to understand genomic imprinting, neurological memory, circadian rhythms, aging, and carcinogenesis. [ABSTRACT FROM AUTHOR]

In spite of increase in milk production, dairy farmers suffer huge economic losses due to mastitis even in very well organized and modern farms. It has been observed that with the increase in the ability of milk production, dairy animals become more susceptible to mastitis. One of the most common causes of mastitis is infection of the mammary gland caused by bacteria like Staphylococcus aureus and Escherichia coli responsible for invoking sub-clinical and clinical mastitis, respectively. The resistivity or susceptibility of species/breeds towards mastitis depends on mode and intensity of immune response to invading pathogens. Inflammation of the mammary tissue results in the release of several cytokines, among which release of interleukin 10 (IL-10) has been identified as an important cytokine for the control of immune response. The present study was undertaken to evaluate the level of IL-10 expression when Peripheral Blood Mononuclear Cells (PBMCs) isolated from Crossbred cattle, Tharparkar cattle and Murrah buffalo were stimulated by antigens obtained from Staphylococcus aureus and Escherichia coli. The results demonstrated deviations in the level of IL-10 expression among these breeds and species in response to the stimulation by the same dose of antigens. Abbreviation: CMT (California Mastitis Test); ELISA (Enzyme-Linked Immunosorbent Assay); LPS (Lipopolysaccharide); LTA (Lipoteichoic acid); PBMCs (Peripheral Blood Mononuclear cells); PGN (Peptidoglycan); SCC (Somatic Cell Count) [ABSTRACT FROM AUTHOR]

In the present study, to analyze the genomic ROH fragments, haplotypes, inbreeding coefficient and effective population size (Ne), SNP50K data of 72 Vrindavani crossbred cattle strain were obtained. After a quality check, 24,449 biallelic SNPs were retained, which were in HWE, MAF > 0.01 and genotyping rate >95%. A total of 385 ROH were found, and chromosome 25 was mostly covered with 50.86%, while chromosome one was least with 12.42%. We classified ROH into <10Mb, 10-15Mb, 15-20Mb, >20Mb categories and observed a 3% inbreeding coefficient for the population in >20Mb category. Inbreeding from an excess of homozygosity was found to be 6% in the population. Ne was also estimated through Ne Estimator and SNeP and in the recent generation, it was found to be 40 for a census size of 464 cattle. The Ne/Nc ratio was found to be 0.086 and a decreasing trend of Ne was observed for over five generations. 45.95% of the autosomal genome was covered with haplotypic structure with highest total block length in chromosome one and lowest in 28. From all the observations made in this study, it can be concluded that Vrindavani is an admixed cattle strain but have an unstable population structure in the current period. [ABSTRACT FROM AUTHOR]