<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-20T14:58:40Z</responseDate><request verb="GetRecord" identifier="oai:repository.ajou.ac.kr:201003/11813" metadataPrefix="oai_dc">https://repository.ajou.ac.kr/oai/request</request><GetRecord><record><header><identifier>oai:repository.ajou.ac.kr:201003/11813</identifier><datestamp>2024-10-11T02:21:24Z</datestamp><setSpec>com_201003_14372</setSpec><setSpec>com_201003_14368</setSpec><setSpec>col_201003_14373</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
<dc:title>Expanding the genetic code of a mouse</dc:title>
<dc:title>마우스의 확장된 유전자 코드 연구</dc:title>
<dc:creator>이, 순장</dc:creator>
<dc:contributor>박, 찬배</dc:contributor>
<dc:contributor>대학원 의생명과학과</dc:contributor>
<dc:contributor>201324380</dc:contributor>
<dc:contributor>이, 순장</dc:contributor>
<dc:subject>aminoacyl-tRNA synthetase</dc:subject>
<dc:subject>Acetyllysine</dc:subject>
<dc:subject>pyrrolysyl-tRNA</dc:subject>
<dc:subject>nonsense-mediated mRNA decay</dc:subject>
<dc:description>Genetic code expansion has used the site-specific insertion of unnatural amino acids into proteins(Greiss and Chin, 2011). An aminoacyl-tRNA synthetase and a tRNA are used to specifically insert the unnatural amino acid during mRNA translation, in response to an amber stop codon (UAG) placed at a user-defined site in a gene interest (Davis and Chin, 2012) 

In this study, I used Acetyllysine(AcK) as unnatural amino acids, N? -acetyl-lysyl-tRNA synthetase (AcKRS) as AcK-tRNA synthetase, pyrrolysyl-tRNA(PylT) as tRNA from Methanosarcina mazei (Mukai et al., 2008). Amber codon was inserted in GFP that is role of reporter gene. AcKRS aminoacylates PylT , and mRNA encoding  the full-length GFP bearing an amber codon that directs amino acid incopration.  

I created AcKRS, GFP mouse, and generated immortalized MEF(mouse embryonic fibroblast). Immortalized MEF(AcKRS.GPF) was treated by AcK., but GFP signal was not detected. 

I thought that no dectable GFP signal was likely due to the three reasons : First,  AcK did not internalize into the system. Second, AcK can be degraded by deacetylase. Third, mRNA was effected by NMD(nonsense-mediated mRNA decay) that can break mRNA containing amber condons. I find the reason that low GFP expression was due to the degradation of mRNA through NMD 

To investigate GFP signal in AcKRS.GFP mouse I did cryosection and observed by confocal microsope. Because NMD efficiency is various according to organs, I got GFP expression in stomach and muscle in AcKRS.GFP mouse.</dc:description>
<dc:description>I.INTRODUCTION  1 

II.MATERIALS AND METHOD 3 

A. Generation of transgenic mice  3 

B. DNA extraction from mouse tail and genotyping PCR  3 

C. Isolation of primary mouse embryo fibroblast and SV40 immortalization  3 

D. siRNA Transfection  4 

E. Cryosection / Confocal microscope  4 

III.RESULTS  5 

A. Generation of AcKRS.GFP  mouse  5 

B. Conformation of transgenic mouse  8 

C. No dectectable GFP induced by AcK  9 

D. Inhibition of Nonsense-mediated mRNA decay through UPF2 Knock down 12 

E. Detection of GFP signal in AcKRS.GFP mouse by cryosection  15 

IV.DISCUSSION  17 

V. CONCLUSION  18 

REFERENCES  19 

국문요약  21</dc:description>
<dc:description>Master</dc:description>
<dc:date>2015-10-26</dc:date>
<dc:date>2015-10-26</dc:date>
<dc:date>2015</dc:date>
<dc:date>2015</dc:date>
<dc:type>Thesis</dc:type>
<dc:type>Theses</dc:type>
<dc:identifier>http://repository.ajou.ac.kr/handle/201003/11813</dc:identifier>
<dc:identifier>http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000020382</dc:identifier>
<dc:identifier>000000020382</dc:identifier>
<dc:language>en</dc:language>
</oai_dc:dc>
</metadata></record></GetRecord></OAI-PMH>