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Regulation Of Human Cytomegalovirus Major Immediate Early Gene Expression During Lytic Replication
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| 자료유형 | E-Book |
|---|---|
| 개인저자 | Arend, Kyle C. |
| 단체저자명 | The University of North Carolina at Chapel Hill. Microbiology and Immunology. |
| 서명/저자사항 | Regulation Of Human Cytomegalovirus Major Immediate Early Gene Expression During Lytic Replication. |
| 발행사항 | [S.l.] : The University of North Carolina at Chapel Hill., 2018 |
| 발행사항 | Ann Arbor : ProQuest Dissertations & Theses, 2018 |
| 형태사항 | 140 p. |
| 소장본 주기 | School code: 0153. |
| ISBN | 9780438033504 |
| 일반주기 |
Source: Dissertation Abstracts International, Volume: 79-10(E), Section: B.
Advisers: Nathaniel J. Moorman; Mark T. Heise. |
| 요약 | Human cytomegalovirus (HCMV) is a significant cause of disease in immune-compromised adults and immune naive newborns. No vaccine exists to prevent HCMV infection, and current antiviral therapies have toxic side effects that limit the duration and intensity of their use. Expression of the HCMV major immediate early (MIE) proteins, IE1 and IE2, is critical for the establishment of lytic infection and reactivation from viral latency. Defining the mechanisms controlling IE1 and IE2 expression is therefore important for understanding how HCMV regulates its replicative cycle. In Chapter 2 we identified several novel transcripts encoding full-length IE1 and IE2 proteins during HCMV lytic replication. While the canonical MIE mRNA was the most abundant transcript at immediate early times, the novel MIE transcripts accumulated to equivalent levels as the known MIE transcript later in infection and were found associated with polyribosomes. These results expand our understanding of the sequences controlling IE1 and IE2 expression by defining novel transcriptional units controlling the expression of full-length IE1 and IE2 proteins. Beyond transcriptional regulation, relatively little is known about the post-transcriptional mechanisms that control IE1 and IE2 protein synthesis. In Chapter 3 we found that the canonical MIE 5' untranslated region (5' UTR) has a positive role in translation control of reporter genes during transfection. We also found that the MIE 5'UTR was necessary for efficient IE1 and IE2 mRNA translation as well as viral replication during infection. These results demonstrate that the shared 5' UTR of the IE1 and IE2 mRNA is a critical determinant of efficient HCMV replication. Virus-induced changes in infected cells are often driven by changes in cellular kinase activity. In Chapter 4 we applied a kinase capture technique, MIB-MS kinome profiling, to quantitatively measure perturbations in >240 cellular kinases simultaneously in cells infected with HCMV. Based on the kinome data, we identified three compounds currently being studied in clinical trials that inhibited HCMV replication. These results show the utility of MIB-MS kinome profiling for identifying existing kinase inhibitors that can potentially be repurposed as novel antiviral drugs to limit the time and cost of new antiviral drug development. |
| 일반주제명 | Virology. Microbiology. Molecular biology. |
| 언어 | 영어 |
| 기본자료 저록 | Dissertation Abstracts International79-10B(E). Dissertation Abstract International |
| 대출바로가기 | http://www.riss.kr/pdu/ddodLink.do?id=T15013664 |
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| No. | 등록번호 | 청구기호 | 소장처 | 도서상태 | 반납예정일 | 예약 | 서비스 | 매체정보 |
|---|---|---|---|---|---|---|---|---|
| 1 | WE00026369 | DP 576.6 | 가야대학교/전자책서버(컴퓨터서버)/ | 대출불가(별치) |
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