Genome-wide analysis of HNF-4 alpha binding sites in correlation with maturity-onset diabetes of the young
| dc.contributor.advisor | Bálint, Bálint László | |
| dc.contributor.advisordept | Debreceni Egyetem::Általános Orvostudományi Kar::Biokémiai és Molekuláris Biológiai Intézet | hu_HU |
| dc.contributor.author | Trang, Bao Khanh | |
| dc.contributor.department | DE--Népegészségügyi Kar | hu_HU |
| dc.contributor.opponent | Barta, Endre | |
| dc.contributor.opponent | Speer, Gábor | |
| dc.contributor.opponentdept | Debreceni Egyetem::Általános Orvostudományi Kar::Orvosi Mikrobiológiai Intézet | hu_HU |
| dc.date.accessioned | 2014-06-05T08:30:40Z | |
| dc.date.available | 2014-06-05T08:30:40Z | |
| dc.date.created | 2014 | |
| dc.date.issued | 2014-06-05T08:30:40Z | |
| dc.description.abstract | The genome-wide association studies have been stared as one of the most advanced biomedical discovery methods, and ever-since are widely applied for the better understanding of genetic components of various diseases including diabetes. A major limitation of these studies consists in the difficulty to explain the correlation between non-coding Single Nucleotide Polymorphisms (SNPs) and the investigated diseases. Hepatocyte nuclear factor-1 alpha and beta, and -4 (HNF1A, HNF1B, HNF4) mutations have been discovered to be the cause of monogenic diabetes, especially in maturity-onset diabetes of the young (MODY). However little is known about the presence of this disease in association with different motifs of HNF- binding sites. Our aim is to investigate this question on a genomic scale and identify the degree of correlation between HNF binding site variants with MODY. The raw ChIP-seq data of published studies was selected from 5 different sequence repository sites and filtered through a set of criteria before being processed by our analysis pipeline (Endre Barta 13-17. EMBnet. Journal, 2011). Here we present our findings for the HNF-binding sites in the investigated tissues and our identification of SNP-s in the HNF binding sites. Further laboratory experiments are needed to validate the differential binding sites and the impact of the SNP-s on the binding of HNF proteins to their targets. | hu_HU |
| dc.description.corrector | D.É. | |
| dc.description.course | népegészségügyi | hu_HU |
| dc.description.courseact | nappali | hu_HU |
| dc.description.courselang | angol | hu_HU |
| dc.description.degree | MSc/MA | hu_HU |
| dc.format.extent | 33 | hu_HU |
| dc.identifier.uri | http://hdl.handle.net/2437/193825 | |
| dc.language.iso | en | hu_HU |
| dc.subject | HNF-4 | hu_HU |
| dc.subject | diabetes | hu_HU |
| dc.subject.dspace | DEENK Témalista::Orvostudomány | hu_HU |
| dc.subject.dspace | DEENK Témalista::Orvostudomány | hu_HU |
| dc.title | Genome-wide analysis of HNF-4 alpha binding sites in correlation with maturity-onset diabetes of the young | hu_HU |