Browse

Mutagenesis of Ptdss1 Gene, Using CRISPR/Cas9 System in Drosophila
초파리 CRISPR/Cas9 시스템을 이용한 Ptdss1 유전자 돌연변이 제작

DC Field Value Language
dc.contributor.advisor전상학-
dc.contributor.author권아영-
dc.date.accessioned2017-10-31T08:02:49Z-
dc.date.available2020-10-06T09:29:24Z-
dc.date.issued2017-08-
dc.identifier.other000000145517-
dc.identifier.urihttps://hdl.handle.net/10371/137718-
dc.description학위논문 (석사)-- 서울대학교 대학원 사범대학 과학교육과, 2017. 8. 전상학.-
dc.description.abstractDue to the increase in average life expectancy, there is growing interest in research on aging-related diseases, especially neurodegenerative diseases. Phospholipids are a major component of the cell membrane and are also highly concentrated in nerve cells. Phospholipid composition is altered in the brain in neurodegenerative disease. Previous studies have shown that phosphatidylserine synthase1 (ptdss1) mutant Drosophila has characteristics of neurodegenerative disease. However, existing strains of ptdss1 mutants are knockdown mutations created by P-element insertion at regulatory sites, which limits their use in researching the specific role of ptdss1 in neurodegeneration. To determine the more precise function of ptdss1, knockouts with mutations in the coding sequence are necessary. In this study, knockout mutations were constructed using the CRISPR/Cas9 system. For ptdss1 mutagenesis, target site gRNA expression mutations were produced and crossed with a germline-specific Cas9 expression line. In germ cells of the flies carrying both the Cas9 transgene and the gRNA transgene, a Cas9-gRNA complex was formed, making an indel mutation. These flies were crossed with wild type flies to construct heterozygous mutants. Mutant flies were characterized by T7 Endonuclease I assay and DNA sequencing. Three types of knockout mutations were constructed, reducing RNA expression levels to about 70% of wild type flies. They are expected to using model animal to configure out the function of ptdss1.-
dc.description.tableofcontentsI. Introduction 1
1. Phospholipids in neuron 1
2. Phosphatidylserine synthase 1(ptdss1) 4
3. CRISPR/Cas9 System 6
4. Purpose of this research 8
II. Materials and Methods 9
1. Plasmid construction 9
2. Drosophila genetics 12
3. PCR amplification and T7EⅠ Assay 15
4. Quantitative real-time PCR 17
III. Results 19
1. Target Loci and gRNA strain construction 19
2. Indel mutation of Ptdss1 22
3. Predicted amino acid sequences of induced mutations 29
4. Ptdss1 mRNA expression level of mutants 32
IV. Discussion 34
References 36
국문초록 41
-
dc.formatapplication/pdf-
dc.format.extent2634781 bytes-
dc.format.mediumapplication/pdf-
dc.language.isoen-
dc.publisher서울대학교 대학원-
dc.subjectDrosophila-
dc.subjectptdss1-
dc.subjectCRISPR/Cas9-
dc.subjectmutagenesis-
dc.subjectphosphatidylserine-
dc.subject.ddc507-
dc.titleMutagenesis of Ptdss1 Gene, Using CRISPR/Cas9 System in Drosophila-
dc.title.alternative초파리 CRISPR/Cas9 시스템을 이용한 Ptdss1 유전자 돌연변이 제작-
dc.typeThesis-
dc.description.degreeMaster-
dc.contributor.affiliation사범대학 과학교육과-
dc.date.awarded2017-08-
Appears in Collections:
College of Education (사범대학)Dept. of Science Education (과학교육과)Biology (생물전공)Theses (Master's Degree_생물전공)
Files in This Item:
  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse