Pregled bibliografske jedinice broj: 927990
Uspostava rekombinantnih mišjih embrionalnih matičnih stanica u svrhu istraživanja fleksibilnosti DNA
Uspostava rekombinantnih mišjih embrionalnih matičnih stanica u svrhu istraživanja fleksibilnosti DNA, 2018., diplomski rad, diplomski, Prirodoslovno-matematički, Zagreb
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Naslov
Uspostava rekombinantnih mišjih embrionalnih matičnih stanica u svrhu istraživanja fleksibilnosti DNA
(Establishment of recombinant mouse embryonic stem cells for use in DNA flexibility assays)
Autori
Mikičić, Ivan
Vrsta, podvrsta i kategorija rada
Ocjenski radovi, diplomski rad, diplomski
Fakultet
Prirodoslovno-matematički
Mjesto
Zagreb
Datum
19.02
Godina
2018
Stranica
57
Mentor
Stewart, Francis
Neposredni voditelj
Ivančić-Baće, Ivana
Ključne riječi
fleksibilnost DNA ; remodeliranje kromatina ; mišje embrionalne matične stanice ; neuralne matične stanice ; Cre-loxP ; CRISPR-Cas9 ; Southern blot
(DNA flexibility ; chromatin remodeling ; mouse embryonic stem cells ; neural stem cells ; Cre-loxP ; CRISPR-Cas9 ; Southern blot)
Sažetak
Using quantitative measurement of DNA flexibility in HEK293 cells by methods of site-specific recombination and Southern blot, it has been observed that in vivo DNA flexibility is double that of in vitro DNA, which has been ascribed to nucleosomal DNA wrapping and chromatin remodeling. Silencing of development-specific genes by local chromatin remodeling could also cause a change in DNA flexibility. The aim of this Master's thesis was to prepare the mouse embryonic stem cells (mESCs) for the comparison of DNA flexibility with the neural stem cells (NSCs). In this work, gene cloning was used to prepare a series of ten plasmids containing the loxP sites of different distances (from 70 bp to 2359 bp), 5' and 3' homology to Nanog gene and blasticidin resistance gene. β-galactosidase test was used to assess the inducilibity of mESCs containing tamoxifen- inducible CreERT2 recombinase and loxP-lacZ reporter gene, which is utilized for inducibility test and as a reference in flexibility measurement. Also, probes for radioactive Southern blotting were produced by gene cloning. Using gene targeting assisted by CRISPR-Cas9, all 10 targeting constructs were successfully inserted into the mNanog gene, which was verified by Southern blotting. Lastly, a method for additional gene targeting validation based on the polymerase chain reaction was developed.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Ivana Ivančić Baće
(mentor)