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典型文献
The mechanistic target of rapamycin complex 1 pathway involved in hepatic gluconeogenesis through peroxisome-proliferator-activated receptor γ coactivator-1α
文献摘要:
Cattle can efficiently perform de novo generation of glucose through hepatic gluconeogenesis to meet post-weaning glucose demand.Substantial evidence points to cattle and non-ruminant animals being characterized by phylogenetic features in terms of their differing capacity for hepatic gluconeogenesis,a process that is highly efficient in cattle yet the underlying mechanism remains unclear.Here we used a variety of transcriptome data,as well as tissue and cell-based methods to uncover the mechanisms of high-efficiency hepatic gluconeogenesis in cattle.We showed that cattle can efficiently convert propi-onate into pyruvate,at least partly,via high expression of acyl-CoA synthetase short-chain family member 1(ACSS1),propionyl-CoA carboxylase alpha chain(PCCA),methylmalonyl-CoA epimerase(MCEE),methylmalonyl-CoA mutase(MMUT),and succinate-CoA ligase(SUCLG2)genes in the liver(P<0.01).Moreover,higher expression of the rate-limiting enzymes of gluconeogenesis,such as phosphoenolpyruvate carboxykinase(PCK)and fructose 1,6-bisphosphatase(FBP),ensures the efficient operation of hepatic gluconeogenesis in cattle(P<0.01).Mechanistically,we found that cattle liver exhibits highly active mechanistic target of rapamycin complex 1(mTORC1),and the expressions of PCCA,MMUT,SUCLG2,PCK,and FBP genes are regulated by the activation of mTORC1(P<0.001).Finally,our results showed that mTORC1 promotes hepatic gluconeogenesis in a peroxisome proliferator-activated receptor γ coactivator 1α(PGC-1α)dependent manner.Collectively,our results not only revealed an important mechanism responsible for the quantitative differences in the efficiency of hepatic gluco-neogenesis in cattle versus non-ruminant animals,but also established that mTORC1 is indeed involved in the regulation of hepatic gluconeogenesis through PGC-1α.These results provide a novel potential insight into promoting hepatic gluconeogenesis through activated mTORC1 in both ruminants and mammals.
文献关键词:
作者姓名:
Guoyan Wang;Jun Zhang;Shengru Wu;Senlin Qin;Yining Zheng;Chao Xia;Huijun Geng;Junhu Yao;Lu Deng
作者机构:
College of Animal Science and Technology,Northwest A&F University,Yangling,Shaanxi 712100,China
引用格式:
[1]Guoyan Wang;Jun Zhang;Shengru Wu;Senlin Qin;Yining Zheng;Chao Xia;Huijun Geng;Junhu Yao;Lu Deng-.The mechanistic target of rapamycin complex 1 pathway involved in hepatic gluconeogenesis through peroxisome-proliferator-activated receptor γ coactivator-1α)[J].动物营养(英文),2022(04):121-131
A类:
Cattle,propi,onate,ACSS1,propionyl,PCCA,MCEE,SUCLG2,gluco,neogenesis
B类:
mechanistic,target,rapamycin,complex,pathway,involved,hepatic,gluconeogenesis,through,peroxisome,proliferator,activated,receptor,coactivator,can,efficiently,perform,novo,generation,glucose,meet,post,weaning,demand,Substantial,evidence,points,cattle,animals,being,characterized,by,phylogenetic,features,terms,their,differing,capacity,process,that,highly,yet,underlying,remains,unclear,Here,used,variety,transcriptome,data,well,tissue,cell,methods,uncover,mechanisms,efficiency,We,showed,convert,into,least,partly,via,acyl,CoA,synthetase,short,chain,family,member,carboxylase,alpha,methylmalonyl,epimerase,mutase,MMUT,succinate,ligase,liver,Moreover,higher,rate,limiting,enzymes,such,phosphoenolpyruvate,carboxykinase,PCK,fructose,bisphosphatase,FBP,ensures,operation,Mechanistically,found,exhibits,active,mTORC1,expressions,are,regulated,activation,Finally,our,results,promotes,PGC,dependent,manner,Collectively,not,only,revealed,important,responsible,quantitative,differences,versus,but,also,established,indeed,regulation,These,provide,novel,potential,insight,promoting,both,ruminants,mammals
AB值:
0.490422
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