Comparative Analysis of the Liver and Spleen Transcriptomes between Holstein and Yunnan Humped Cattle

Previous studies have shown that Yunnan humped cattle have higher disease resistance than pure taurine cattle, such as Holsteins. However, there exists limited information about the molecular genetic basis underlying disease resistance differences between them. The objective of this study was to com...

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Bibliographic Details
Main Authors: Yanyan Chen, Benjuan Zeng, Peng Shi, Heng Xiao, Shanyuan Chen
Format: Article
Language:English
Published: MDPI AG 2019-08-01
Series:Animals
Subjects:
Online Access:https://www.mdpi.com/2076-2615/9/8/527
Description
Summary:Previous studies have shown that Yunnan humped cattle have higher disease resistance than pure taurine cattle, such as Holsteins. However, there exists limited information about the molecular genetic basis underlying disease resistance differences between them. The objective of this study was to compare differentially expressed genes (DEGs) in the liver and spleen tissues of Holstein and Yunnan humped cattle through comparative transcriptome analysis, using RNA-sequencing. In total, 1564 (647 up- and 917 down-regulated genes) and 1530 (716 up- and 814 down-regulated genes) DEGs were obtained in the liver and spleen tissues of Holstein and Yunnan humped cattle comparison groups, respectively. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis showed that the DEGs were mainly associated with the RIG-I signaling pathway, immune responses, major histocompatibility complex (MHC) class I protein complex and complement activation, human T-cell lymphotropic virus type-I (HTLV-I) infection. Some genes related to immune function, such as <i>C1QB</i>, <i>CD55</i>, <i>MASP2</i>, <i>C4BPA</i>, <i>MAVS</i>, <i>NOD2</i>, and <i>CD46</i>, were up-regulated in Yunnan humped cattle, while <i>C2</i>, <i>SERPING1</i>, <i>SERPINE1</i>, <i>TIRAP</i>, <i>TLR2</i>, and <i>TLR6</i> were down-regulated. The expression levels of 11 selected DEGs, analyzed by quantitative reverse-transcription polymerase chain reaction (RT-qPCR), were consistent with the deep sequencing results by RNA-sequencing. Our results will provide a scientific basis and key technical support for disease-resistant breeding of domestic cattle.
ISSN:2076-2615