机构地区:[1]College of Animal Science and Technology, Northeast Agricultural University, Harbin 150030, China
出 处:《Journal of Northeast Agricultural University(English Edition)》2011年第1期46-51,共6页东北农业大学学报(英文版)
基 金:Supported by National 973 Project of China (2006CB102105);Natural Science Foundation Key Project of Heilongjiang Province (ZJN0604-01);National 863 Project of China (2006AA10A120)
摘 要:The nuclear receptor peroxisome proliferator-activated receptor γ(PPAR-γ) is a key transcriptional regulator of adipocyte differentiation.It also modulates the synthesis of adipocytokines in the adipose tissue.Its polymorphisms are associated with the risk of type Ⅱ diabetes,obesity,cardiovascular diseases and cancer.In the present study,to investigate the regulatory mechanism of PPAR-γ gene on lipid metabolism,the computational prediction of peroxisome proliferator response elements(PPREs) was pursued with a genome-wide scale by using MEME/MAST method based on the information of TRANSFAC database,then GO and KEGG analyses were carried out.The results showed that a huge number of predicted target genes of PPAR-γ were significantly enriched in 36 GO terms(P〈0.05) and 10 KEGG pathways(P〈0.05) which were related closely to the lipid metabolism.The results should be a valuable resource for elucidation of the regulatory mechanism of PPAR-γ influence on lipid metabolism,also of the major importance to the diagnosis,prevention and treatment of the complex diseases such as obesity and diabete.The nuclear receptor peroxisome proliferator-activated receptor γ(PPAR-γ) is a key transcriptional regulator of adipocyte differentiation.It also modulates the synthesis of adipocytokines in the adipose tissue.Its polymorphisms are associated with the risk of type Ⅱ diabetes,obesity,cardiovascular diseases and cancer.In the present study,to investigate the regulatory mechanism of PPAR-γ gene on lipid metabolism,the computational prediction of peroxisome proliferator response elements(PPREs) was pursued with a genome-wide scale by using MEME/MAST method based on the information of TRANSFAC database,then GO and KEGG analyses were carried out.The results showed that a huge number of predicted target genes of PPAR-γ were significantly enriched in 36 GO terms(P〈0.05) and 10 KEGG pathways(P〈0.05) which were related closely to the lipid metabolism.The results should be a valuable resource for elucidation of the regulatory mechanism of PPAR-γ influence on lipid metabolism,also of the major importance to the diagnosis,prevention and treatment of the complex diseases such as obesity and diabete.
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