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Paradigm of Time-sequence Development of the Intestine of Suckling Piglets with microarray
SUN Yunzi 1 #,YU Bing 2,ZHANG Keying 1,HE Jun 3,CHEN Xijian 4,CHEN Daiwen 3 *
1.Animal Nutrition Institute, Sichuan Agricultural University; Key Lab of Animal Disease Resistance Nutrition Of China Education Ministry
2.Husbandry Bureau of Liupanshui City of Guizhou
3.Animal Nutrition Institute, Sichuan Agricultural University
4.Genminix Informatics Ltd.Co
*Correspondence author
#Submitted by
Subject:
Funding: 高等学校博士学科点专项科研基金(No.20070626003)
Opened online: 1 March 2011
Accepted by: none
Citation: SUN Yunzi,YU Bing,ZHANG Keying.Paradigm of Time-sequence Development of the Intestine of Suckling Piglets with microarray[OL]. [ 1 March 2011] http://en.paper.edu.cn/en_releasepaper/content/4411626
 
 
The interaction of the genes involved in intestinal development is the molecular basis of the regulatory mechanisms of intestinal development. The objective of this study was to identify the significant pathways and key genes that regulate intestinal development in Landrace piglets, and then to elucidate their rules of operation. The differential expression of genes related to intestinal development during suckling was investigated using a porcine genome array. Time sequence profiles were then analyzed for the differentially expressed genes to obtain significant expression profiles. Subsequently, the most significant profiles were assayed using Gene Ontology categories, pathway analysis, network analysis, and analysis of gene co-expression to unveil the main biological processes, the significant pathways, and the effective genes, respectively. In addition, quantitative real-time PCR was carried out to verify the reliability of the results of the analysis of the array. The results showed that more than 8000 differential expression transcripts were identified using microarray technology. Among the 30 significant model profiles obtained, profiles 66 and 13 were the most significant. Analysis of profiles 66 and 13 indicated that they were mainly involved in immunity, metabolism, and cell division or proliferation. Among the most effective genes in these two profiles, CN161469, which is similar to methylcrotonoyl-Coenzyme A carboxylase 2 (beta), and U89949.1, which encodes a folate binding protein, had a crucial influence on the co-expression network.
Keywords:intestinal development; microarray; gene; expression profile; network
 
 
 

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