De novo genome assembly depicts the immune genomic characteristics of cattle

Immunogenomic loci remain poorly understood because of their genetic complexity and size. Here, we report the de novo assembly of a cattle genome and provide a detailed annotation of the immunogenomic loci. The assembled genome contains 143 contigs (N50 ~ 74.0 Mb). In contrast to the current referen...

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Veröffentlicht in:Nature communications 2023-10, Vol.14 (1), p.6601-6601, Article 6601
Hauptverfasser: Li, Ting-Ting, Xia, Tian, Wu, Jia-Qi, Hong, Hao, Sun, Zhao-Lin, Wang, Ming, Ding, Fang-Rong, Wang, Jing, Jiang, Shuai, Li, Jin, Pan, Jie, Yang, Guang, Feng, Jian-Nan, Dai, Yun-Ping, Zhang, Xue-Min, Zhou, Tao, Li, Tao
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Sprache:eng
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Zusammenfassung:Immunogenomic loci remain poorly understood because of their genetic complexity and size. Here, we report the de novo assembly of a cattle genome and provide a detailed annotation of the immunogenomic loci. The assembled genome contains 143 contigs (N50 ~ 74.0 Mb). In contrast to the current reference genome (ARS-UCD1.2), 156 gaps are closed and 467 scaffolds are located in our assembly. Importantly, the immunogenomic regions, including three immunoglobulin (IG) loci, four T-cell receptor (TR) loci, and the major histocompatibility complex (MHC) locus, are seamlessly assembled and precisely annotated. With the characterization of 258 IG genes and 657 TR genes distributed across seven genomic loci, we present a detailed depiction of immune gene diversity in cattle. Moreover, the MHC gene structures are integrally revealed with properly phased haplotypes. Together, our work describes a more complete cattle genome, and provides a comprehensive view of its complex immune-genome. The genomic organisation of the cattle genome has been assembled to a limited level of resolution. Here using long range nanopore sequencing the authors present a cattle genome assembly concentrating on characterising the immunogenomic loci, particularly T cell receptor (TR), immunoglobulin (IG) and MHC genes, from one animal.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-023-42161-1