東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Complex gene expression and interpla...

Caviness, Katie E.

FindBook

Google Book

Amazon

博客來

Complex gene expression and interplay of the UL136 protein isoforms influence human cytomegalovirus persistence.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Complex gene expression and interplay of the UL136 protein isoforms influence human cytomegalovirus persistence./
作者:	Caviness, Katie E.
面頁冊數:	191 p.
附註:	Source: Dissertation Abstracts International, Volume: 76-09(E), Section: B.
Contained By:	Dissertation Abstracts International76-09B(E).
標題:	Virology. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3700926
ISBN:	9781321711738

Complex gene expression and interplay of the UL136 protein isoforms influence human cytomegalovirus persistence.
Caviness, Katie E.

Complex gene expression and interplay of the UL136 protein isoforms influence human cytomegalovirus persistence. - 191 p.

Source: Dissertation Abstracts International, Volume: 76-09(E), Section: B.

Thesis (Ph.D.)--The University of Arizona, 2015.

This item must not be sold to any third party vendors.

Human cytomegalovirus (HCMV), a beta herpesvirus, persists indefinitely in the human host through a life-long, latent infection. HCMV is associated with life threatening pathologies in the immune naive or compromised and, therefore, understanding of the mechanisms of viral persistence is imperative to human health. The ULb' region of the HCMV genome is selectively lost in high-passage strains of the virus, yet retained in low-passage strains. As such, the ULb' is hypothesized to play a role in immune evasion, pathogenesis, latency, and dissemination. ULb' encoded viral products are poorly characterized, hindering a mechanistic understanding of HCMV persistence.

ISBN: 9781321711738Subjects--Topical Terms:

642304
Virology.

Complex gene expression and interplay of the UL136 protein isoforms influence human cytomegalovirus persistence.
LDR:03892nmm a2200325 4500 001 2066504
005 20151106144909.5
008 170521s2015 ||||||||||||||||| ||eng d
020 $a 9781321711738
035 $a (MiAaPQ)AAI3700926
035 $a AAI3700926
040 $a MiAaPQ $c MiAaPQ
100 1 $a Caviness, Katie E. $3 3181311
245 1 0 $a Complex gene expression and interplay of the UL136 protein isoforms influence human cytomegalovirus persistence.
300 $a 191 p.
500 $a Source: Dissertation Abstracts International, Volume: 76-09(E), Section: B.
500 $a Adviser: Felicia Goodrum.
502 $a Thesis (Ph.D.)--The University of Arizona, 2015.
506 $a This item must not be sold to any third party vendors.
506 $a This item must not be added to any third party search indexes.
520 $a Human cytomegalovirus (HCMV), a beta herpesvirus, persists indefinitely in the human host through a life-long, latent infection. HCMV is associated with life threatening pathologies in the immune naive or compromised and, therefore, understanding of the mechanisms of viral persistence is imperative to human health. The ULb' region of the HCMV genome is selectively lost in high-passage strains of the virus, yet retained in low-passage strains. As such, the ULb' is hypothesized to play a role in immune evasion, pathogenesis, latency, and dissemination. ULb' encoded viral products are poorly characterized, hindering a mechanistic understanding of HCMV persistence.
520 $a We previously defined a 3.6-kb locus spanning UL133-UL138 within the ULb' region important to viral latency. UL136 is expressed as five protein isoforms ranging from 33-kDa to 19-kDa, arising from alternative transcription and translation mechanisms. We mapped the origins of each isoform through advanced bacterial artificial chromosome recombineering, where each ATG was disrupted and the resulting UL136 recombinant virus was screened for altered expression of the pUL136 isoforms. Remarkably, 8 of the 11 potential translation initiation sites encoded within the ORF are utilized to create the pUL136 isoforms. The pUL136 isoforms have distinct localization and trafficking patterns within the cell, including varying degrees of Golgi association, suggesting each isoform may interface with different cellular components and pathways. Further characterization of UL136 recombinant viruses revealed a complex, antagonistic relationship between the pUL136 isoforms. In endothelial cells, which are important to viral persistence and dissemination due to their ability to maintain a slow, "smoldering" infection, the 33- and 26-kDa isoforms promote replication, while the 25-kDa isoform enhances their combined activity, and the 23-/19-kDa isoforms repress the activity of the 25-kDa isoform. The pUL136 isoforms are also required for virus maturation in endothelial cells, where the 33-kDa is required both for virion envelopment and efficient formation of the perinuclear viral assembly compartment. In both an in vitro CD34 + cell culture model of latency and an in vivo NOD-scid IL2Rgammacnull humanized mouse model, a virus lacking the 23-/19-kDa isoforms fails to establish latency, instead replicating and disseminating with increased efficiency while viruses lacking the 33- and 26-kDa isoforms fail to efficiently reactivate or disseminate. Our data suggest that the interplay between the pUL136 isoforms maintains an intricate balance of infection that governs replication, latency, and virus dissemination, which ultimately contributes to the role of the UL133/8 locus in mediating outcomes of HCMV infection.
590 $a School code: 0009.
650 4 $a Virology. $3 642304
650 4 $a Genetics. $3 530508
650 4 $a Cellular biology. $3 3172791
690 $a 0720
690 $a 0369
690 $a 0379
710 2 $a The University of Arizona. $b Genetics. $3 3181312
773 0 $t Dissertation Abstracts International $g 76-09B(E).
790 $a 0009
791 $a Ph.D.
792 $a 2015
793 $a English
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3700926