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   The Response of Murine Embryonic Fibroblast To Abnormal Expression of Yamanaka Factors  
   
DOR 20.1001.2.9920068682.1399.1.1.426.0
نویسنده Ashtarnakhaei Mohammadvala ,Farivar Shirin
منبع ژنتيك ايران - 1399 - دوره : 16 - شانزدهمین کنگره و چهارمین کنگره بین المللی ژنتیک ایران - کد همایش: 99200-68682
چکیده    Background and aim: it remains unclear how the ectopic expression of defined transcription factors induces dynamic changes in gene expression profiles that establish a pluripotent state during direct cell reprogramming. several reports have shown that reprogramming is a multistep process that includes accelerated cell proliferation, morphological changes of the cells, a mesenchymal-to-epithelial transition (met), and unidentified stochastic events. transcription factors often act in concert with cofactors and modifiers to turn the gene expression on or off. in a recent study microarrays related to expression of genes in mouse embryonic fibroblasts which were infected with vectors containing transcription factors oct4, sox2, klf4, c-myc were published. its results were obtained in the form of a dataset and analyzed.methods: a raw dataset has been extracted from geo datasets (ncbi). in its heat map the genes which had the most difference in terms of expression were selected and they were subjected to further analysis including protein associated networks in string-db. and also geo2r results were analyzed with string network package.results: as it was previously determined, transcription factors are the means for regulation of gene expression. but the result, i.e. 147 gene sets out of 1515, showed that there is a negative regulation on gene expression when the cells are exposed to yamanaka factors. moreover, 11 gene sets out of 44, are contributed to the inhibition of dna methylation when embryonic fibroblast is subjected to above-maintained factors. the results demonstrate that after several days, the expression of genes related to dna repair system changes remarkably in embryonic fibroblasts which were infected with retroviruses. it is of great value to consider that also expression of genes related to pathways like “cellular response to dna damage stimulus” had changed dramatically, since the cells were infected. there are also other genes in which their expression changes after infecting the cells with the above-mentioned vectors. these genes are somehow related to “histone demethylase activity (h3-k9 specific)” pathway and it shows that infecting cells with those viruses can result in epigenetic regulation of gene expression.conclusion: the process of dna demethylation and the activation of histone demethylase could be hallmark during the dedifferentiation. and also the results which were mentioned shows the metabolic pathways could be cooperating with dna repair. as science improves in ipsc field, the demand toward knowing more about its mechanisms grows.
کلیدواژه Dedifferentiation
آدرس Shahid Beheshti University, Iran, Shahid Beheshti University, Iran
 
     
   
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