prikaz prve stranice dokumenta Ciljana modulacija CpG metilacije gena HNF1A upotrebom molekularnog alata CRISPR/dCas9- TET1 i utjecaj na njegovu transkripciju
  Download
PDF 1.86 MB
master's thesis
Ciljana modulacija CpG metilacije gena HNF1A upotrebom molekularnog alata CRISPR/dCas9- TET1 i utjecaj na njegovu transkripciju
Zagreb: University of Zagreb, Faculty of Science, 2020. urn:nbn:hr:217:218306
Barberić, Tomislav
University of Zagreb
Faculty of Science
Department of Biology

Institutional repository: Repository of the Faculty of Science

Cite this document

Barberić, T. (2020). Ciljana modulacija CpG metilacije gena HNF1A upotrebom molekularnog alata CRISPR/dCas9- TET1 i utjecaj na njegovu transkripciju (Master's thesis). Zagreb: University of Zagreb, Faculty of Science. Retrieved from https://urn.nsk.hr/urn:nbn:hr:217:218306

Barberić, Tomislav. "Ciljana modulacija CpG metilacije gena HNF1A upotrebom molekularnog alata CRISPR/dCas9- TET1 i utjecaj na njegovu transkripciju." Master's thesis, University of Zagreb, Faculty of Science, 2020. https://urn.nsk.hr/urn:nbn:hr:217:218306

Barberić, Tomislav. "Ciljana modulacija CpG metilacije gena HNF1A upotrebom molekularnog alata CRISPR/dCas9- TET1 i utjecaj na njegovu transkripciju." Master's thesis, University of Zagreb, Faculty of Science, 2020. https://urn.nsk.hr/urn:nbn:hr:217:218306

Barberić, T. (2020). 'Ciljana modulacija CpG metilacije gena HNF1A upotrebom molekularnog alata CRISPR/dCas9- TET1 i utjecaj na njegovu transkripciju', Master's thesis, University of Zagreb, Faculty of Science, accessed 11 September 2024, https://urn.nsk.hr/urn:nbn:hr:217:218306

Barberić T. Ciljana modulacija CpG metilacije gena HNF1A upotrebom molekularnog alata CRISPR/dCas9- TET1 i utjecaj na njegovu transkripciju [Master's thesis]. Zagreb: University of Zagreb, Faculty of Science; 2020 [cited 2024 September 11] Available at: https://urn.nsk.hr/urn:nbn:hr:217:218306

T. Barberić, "Ciljana modulacija CpG metilacije gena HNF1A upotrebom molekularnog alata CRISPR/dCas9- TET1 i utjecaj na njegovu transkripciju", Master's thesis, University of Zagreb, Faculty of Science, Zagreb, 2020. Available at: https://urn.nsk.hr/urn:nbn:hr:217:218306

Metadata
TitleCiljana modulacija CpG metilacije gena HNF1A upotrebom molekularnog alata CRISPR/dCas9- TET1 i utjecaj na njegovu transkripciju
Title (english)Targeted modulation of HNF1A gene's CpG methylation using CRISPR/dCas9-TET1 molecular tool and effect on its transcription
AuthorTomislav Barberić
MentorVlatka Zoldoš (mentor)
Committee memberVlatka Zoldoš (predsjednik povjerenstva)
Committee memberDomagoj Đikić (član povjerenstva)
Committee memberAna Previšić (član povjerenstva)
Committee memberMirta Tkalec (član povjerenstva)
GranterUniversity of Zagreb
Faculty of Science
(Department of Biology)
Zagreb
Defense date and country2020-02-27, Croatia
Scientific / art field,
discipline and subdiscipline		NATURAL SCIENCES
Biology
Abstract
HNF1α je transkripcijski faktor koji sudjeluje u regulaciji ekspresije mreže gena uključenih u niz molekularnih i metaboličkih procesa u jetri, gušterači, crijevima i bubrezima. U β stanicama gušterače, mutacije u genu HNF1A vode do poremećaja otpuštanja inzulina uslijed stimulacije glukozom, a fenotip u ljudi je dijabetes tip MODY3. Pretpostavlja se da bi epigenetičko utišavanje gena HNF1A metilacijom moglo imati isti efekt na ekspresiju gena te fenotip kao i genska mutacija. Ovo istraživanje imalo je za cilj transfecirati staničnu liniju 1.1B4, model za istraživanje β stanica gušterače, fuzijskim proteinom TET1-dCas9 te istražiti dolazi li do promjene metilacije na 4 CpG mjesta koja su prijašnjim korelacijskim analizama otkrivena kao kandidat regulatorna mjesta za transkripcijsku aktivnost gena HNF1A. U tu svrhu naveo sam fuzijski protein TET1-dCas9 pomoću jedne molekule sgRNA na 4 kandidat CpG mjesta u 1. egzonu gena HNF1A. Nakon uspješne transfekcije analizirao sam metilaciju citozina pirosekvenciranjem nakon bisulfitne konverzije molekule DNA te sam potvrdio smanjenje stupnja metilacije na sva 4 CpG mjesta u periodu od 30 dana nakon transfekcije stanica 1.1B4. Također sam analizirao razinu transkripcije pomoću metode RT-qPCR upotrebom proba TaqMan te utvrdio povećanu razinu transkripcijske aktivnosti gena HNF1A u uspješno transfeciranim stanicama. Rezultati ovog istraživanja potvrđuju da epigenetička manipulacija 4 kandidat CpG mjesta dovodi do povećanja transkripcijske aktivnosti gena HNF1A što ukazuje na regulatornu ulogu ova 4 CpG mjesta u stanicama 1.1B4.
Abstract (english)
HNF1α is a transcription factor involved in regulating the expression of a network of genes involved in a number of molecular and metabolic processes in the liver, pancreas, intestines and kidneys. Mutations in the HNF1A gene lead to impaired glucose stimulated insulin secretion in pancreatic β cells, and the resulting phenotype in humans is MODY3 type diabetes. It is hypothesized that epigenetic silencing of the HNF1A gene could have the same effect on gene expression and phenotype as the gene mutation. The aim of this study was to transfect 1.1B4 cells, which serve as a model for pancreatic β cells, with a TET1-dCas9 fusion protein in order to change methylation level on the 4 CpG sites that previous corelation studies identified as candidate regulatory sites for the transcription activity of the HNF1A gene. To achieve this, TET1-dCas9 fusion protein was targeted to the 4 candidate CpG sites in the 1st exon of the HNF1A gene by using a single sgRNA. Analysis of DNA methylation by pirosequencing after bisulphate DNA conversion confirmed a decrease in the methylation levels at all 4 CpG sites during the 30 day period following transfection. RT-qPCR method using TaqMan probes revealed an increase of HNF1A transcriptional activity following the epigenetic manipulation with TET1-dCas9. The results of this study showed that epigenetic manipulation of the 4 candidate CpG sites leads to an increase in the HNF1A gene transcriptional activity, which confirms a regulatory role of these 4 CpG sites for HNF1A expression in 1.1B4 cells.
Keywords
Keywords (english)
Languagecroatian
URN:NBNurn:nbn:hr:217:218306
Study programmeTitle: Molecular Biology
Study programme type: university
Study level: graduate
Academic / professional title: magistar/magistra molekularne biologije (magistar/magistra molekularne biologije)
Type of resourceText
File originBorn digital
Access conditionsOpen access
Embargo expiration date: 2022-02-27
Terms of useLicence In copyright icon
Created on2020-07-13 07:22:47