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Journal of Veterinary and Animal Sciences

Volume: 51 Issue: 2

  • Open Access
  • Research Article

Exome wide variant discovery by next generation dna sequencing in Vechur cattle of Kerala

R. S. Reshma1, T. V. Aravindakshan2, G. Radhika3, T. Naicy4 and K. Raji5

1. MVSc scholar, Animal Biotechnology, CVAS, Mannuthy. Ph.7902875712 2. Director, Centre for Advanced studies in Animal Genetics and Breeding 3. Associate Professor, Centre for Advanced studies in Animal Genetics and Breeding 4. Assistant Professor, Department of Animal Genetics and Breeding and corresponding author Ph.No. 9446119307, [email protected] 5. Associate Professor, Department of Veterinary Physiology

Year: 2020, Page: 201-206,

Received: June 2, 2020 Accepted: June 28, 2020 Published: July 1, 2020

Abstract

Vechur, the native cattle breed of Kerala, India is well-known for economically valuable phenotypic traits like disease resistance, adaptability to hot and humid tropical climatic conditions, low feed requirements and high quality milk. However, genomic information underlying these traits is rare. In the present study, the whole exome sequencing of a Vechur cow using Illumina HiSeq 2500 platform is reported. Comparison of sequences with Bos taurus reference genome assembly (UMD 3.1) identified 1,716,847 variants including 1,578,749 Single Nucleotide Polymorphisms and 138,098 Insertion/Deletions, of which 359,034 variants (20.91%) were novel. Detailed annotation of the identified variants showed that majority were situated in the intergenic region. Out of the 724,808 variants found inside the gene region, 107,880 were exonic variants. In the exonic variant, substantial proportion of non-synonymous (34.83%), frameshift (12.47%), nonsense (0.3%), start loss (0.06%) and stop loss (0.0009%) variants were identified. This information will provide a better understanding of genetic differences responsible for the peculiar phenotypic traits inherent to Vechur cattle.

Keywords: Whole-exome sequencing, Vechur cattle, disease resistance, adaptability

References

Bodi, K., Perera, A.G., Adams, P.S., Bintzler, D., Dewar, K., Grove, D.S., Kieleczawa, J., Lyons, R.H., Neubert, T.A., Noll, A.C., Singh, S., Steen, R. and Zianni, M. 2013. Comparison of Commercially Available Target Enrichment Methods for NextGeneration Sequencing. J. Biomol. Tech. 24:73–86.

Choi, J.W., Chung, W.H., Lee, K.T., Choi, J.W., Jung, K.S., Cho, Y., Kim, N. and Kim, T.H. 2013. Whole Genome Resequencing of Heugu (Korean Black Cattle) for the Genome-Wide SNP Discovery. Korean J. Food Sci. An. 33:715-722.

Choi, J.W., Liao, X., Stothard, P., Chung, W.H., Jeon, H.J., Miller, S.P., Choi, S.Y., Lee, J.K., Yang, B., Lee, K.T., Han, K.J., Kim, H.C., Jeong, D., Oh, J.D., Kim, N., Kim, T.H., Lee, H.K. and Lee, S.J. 2014. WholeGenome Analyses of Korean Native and Holstein Cattle Breeds by Massively Parallel Sequencing. PLoS ONE doi: 10.1371/journal.pone.0101127

Choi, J.W., Choi, B.H., Lee, S.H., Lee, S.S., Kim, H.C., Yu, D., Chung, W.H., Lee, K.T., Chai, H.H., Cho, Y.M. and Lim, D. 2015. Whole-Genome Resequencing Analysis of Hanwoo and Yanbian Cattle to Identify Genome-Wide SNPs and Signatures of Selection. Mol. Cells. 38 : 466-473.

Eck, S.H., Benet-Pagès, A., Flisikowski, K., Meitinger, T., Fries, R. and Strom, T.M. 2009. Whole genome sequencing of a single Bos taurus animal for single nucleotide polymorphism discovery. Genome Biol. 10 : R82.1- R82.8.

Gao, X., Xu, J. and Starmer, J. 2015. Notes. Fastq2vcf: a concise and transparent pipeline for whole-exome sequencing data analyses. BMC Res. Notes. 8:72- 76.

Kraus, R.H.S., Kerstens, H.H.D., Hooft, P.V., Crooijmans, R.P.M.A., Poel, J.J.V.D., Elmberg, J., Vignal, A., Huang, Y., Li, N., Prins, H.H.T. and Groenen, M.A.M. 2011. Genome wide SNP discovery, analysis and evaluation in mallard (Anas platyrhynchos). BMC Genomics. 12:150

Lee, C.Y., Chiu, Y.C., Wang, L.B., Kuo, Y.L., Chuang, E.Y., Lai, L.C. and Tsai, M.H. 2013. Common applications of nextgeneration sequencing technologies in genomic research. Transl. Cancer Res. 2 : 33- 45.

Li, H., Ruan, J. and Durbin, R. 2008. Mapping short DNA sequencing reads and calling variants using mapping quality scores. Genome Res. 18:1851-1858.

Li, H., Handsaker, B., Wysoker, A., Fennell, T., Ruan, J., Homer, N., Marth, G., Abecasis, G.,and Durbin, R. 2009. 1000 Genome Project Data. The Sequence Alignment/Map format and SAMtools. Bioinformatics. 25: 2078–2079.

Liu, Q., Guo, Y., Li, J., Long, J., Zhang, B. and Shyr, Y. 2012. Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data. BMC Genomics. 13 : 1-8.

McTavish, E.J., Decker, J.E., Schnabel, R.D., Taylor, J.F. and Hillis, D.M. 2013. New World cattle show ancestry from multiple independent domestication events. Proc. Natl. Acad. Sci. 110: E1398-E1406.

Nayarisseri, A., Yadav, M., Bhatia, M., Pandey, A., Elkunchwar, A., Paul, N., Sharma, D. and Kumar, G. 2013. Impact of NextGeneration Whole-Exome sequencing in molecular diagnostics. Drug Invent. Today. 5: 327-334.

O’Rawe, J., Jiang, T., Sun, G., Wu, Y., Wang, W., Hu, J., Bodily, P., Tian, L., Hakonarson, H., Johnson, W.E., Wei, Z., Wang, K. and Lyon, G.J. 2013. Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing. Genome Med. 5: 1-18.

Parla, J.S., Iossifov, I., Grabill, I., Spector, M.S., Kramer, M. and McCombie, W.R. 2011. A comparative analysis of exome capture. Genome Biol. 12:1-17.

Parmley, J.L. and Hurst, L.D. 2007. How do synonymous mutations affect fitness? BioEssays. 29:515–519. Raghunandanan, K.V. 2006. Vechur cattle of Kerala. The Indian Cow. 7:48-49.

Stothard, P., Choi, J., Basu, U., SumnerThomson, J.M., Meng, Y., Liao, X. and Moore, S.S. 2011. Whole genome resequencing of Black Angus and Holstein cattle for SNP and CNV discovery. BMC Genomics. 12:559

Schwarzenbacher, H., Burgstaller, J., Seefried, F.R., Wurmser, C., Hilbe, M., Jung, S., Fuerst, C., Dinhop, N., Weissenböck, H., Fuerst-Walt, B., Doleza, M., Winkler, R., Grueter, O., Bleu, U., Wittek, T., Fries R. and Pausch, H. 2016. A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle. BMC Genomics. 17:400. doi 10.1186/s12864-016-2742-y.

Warr, A., Robert, C., Hume, D., Archibald, A., Deeb, N. and Watson, M. 2015. Exome Sequencing: Current and Future Perspectives. Genes Genomes Genet. 5:1543-1549.

Zhou, Q., Su, X., Wang, A., Xu, J. and Ning, K. 2013. QC-Chain: Fast and Holistic Quality Control Method for NextGeneration Sequencing Data. PLoS ONE. 8 :1

Cite this article

Reshma, R. S., Aravindakshan, T. V., Radhika, G., Naicy, T. and Raji, K.2020. Exome wide variant discovery by next generation dna sequencing in Vechur cattle of Kerala. J. Vet. Anim. Sci. 51(2): 201-206.

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