In silico Mining of Protein-coding and Non-coding RNA (ncRNA) Specific Genes in Exotic versus Indigenous Gaddi Dogs

Shilpa Tewari, Chandra Shekhar Mukhopadhyay
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Abstract

Background: Comparative functional genomics will aid in the molecular identification of diverse dog breeds. Methods: The current proposal aimed at conducting a differential study between the genomes of exotic canines (Labrador, Basenji, Tasha-Boxer breed, Mischka breed German Shepherd, Zoey breed Great Dane) and indigenous (Gaddi) breeds through whole genome annotation. Result: The prediction analysis by GeneMark tool yielded an average of 46484 transcripts, in Gaddi dogs and exotic breeds ranging from 29669 to 30956. A total of 57 miRNAs were discovered in exotic breeds and 22 miRNAs in Gaddi dogs, 18 are common in both, while 4 were unique to Gaddi dogs. lncRNA was predicted using the PLEK, CPAT, and LGC tools, resulting in 3201, 396, and 4188 noncoding sequences in exotic breeds, respectively. Approximately, 31 thousand lncRNA transcripts were identified in the Gaddi dog genome. Microsatellites were found to be distributed through approximately 0.3% of both genomes. The average island length of CpG ranged between 24246.48 to 28080.66 in exotic breeds at chromosome level assembly and 697.15 in indigenous Gaddi dogs at contig level assembly. The predicted protein-coding genes were subjected to pathway analysis by DAVID and PANTHER. Five genes that are expressed in the blood (INSL3, CLDN3, MYH1, CLN5, and GALC) were selected for validation through qPCR. The results indicated that the genes were expressed in both groups. Conclusion: The study is the maiden report on the comparative genome analysis between indigenous Gaddi dogs and exotic dog breeds. The findings set the stage for further research into the known and novel genes, which might be employed as biomarkers for disease diagnosis and to investigate their regulatory role. other: Acknowledgment: The authors gratefully acknowledge the funding provided by the Department of Biotechnology, Government of India, through the collaborative research project “Parentage Determination and Cytogenetic Profiling in Dogs (DBT-19I)” and Dr. S.K Mahajan, who assisted with sample collection, deserves special recognition.
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外来加迪犬与本地加迪犬蛋白质编码和非编码RNA (ncRNA)特异性基因的计算机挖掘
背景:比较功能基因组学将有助于不同犬种的分子鉴定。方法:本提案旨在通过全基因组注释对外来犬(拉布拉多、巴森吉、塔沙-拳师犬、米什卡犬、德国牧羊犬、佐伊犬)和本土犬(加迪犬)的基因组进行差异研究。结果:通过GeneMark工具进行预测分析,平均得到46484个转录本,在Gaddi犬和外来犬种中,转录本的数量在29669 ~ 30956之间。在外来品种中发现了57种mirna,在Gaddi犬中发现了22种mirna,其中18种在两者中都是常见的,而4种在Gaddi犬中是独特的。使用PLEK、CPAT和LGC工具预测lncRNA,在外来品种中分别得到3201、396和4188个非编码序列。大约有31000个lncRNA转录本在Gaddi狗基因组中被鉴定出来。发现微卫星分布在大约0.3%的两个基因组中。在染色体水平上,外来犬种CpG的平均岛长在24246.48 ~ 28080.66之间,在群水平上,本地犬的CpG岛长为697.15。预测的蛋白编码基因由DAVID和PANTHER进行通路分析。选择在血液中表达的5个基因(INSL3、CLDN3、MYH1、CLN5和GALC),通过qPCR进行验证。结果表明,这些基因在两组中均有表达。结论:本研究首次报道了本地加迪犬和外来犬种的基因组比较分析。这一发现为进一步研究已知和新基因奠定了基础,这些基因可能被用作疾病诊断的生物标志物,并研究它们的调节作用。致谢:作者感谢印度政府生物技术部通过合作研究项目“狗的亲子鉴定和细胞遗传学分析(DBT-19I)”提供的资金,并特别感谢S.K Mahajan博士协助收集样本。
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