Suppr超能文献

豚鼠巨细胞病毒 GP84 是人类巨细胞病毒(HCMV)UL84 基因的功能同源物,可在嵌合 HCMV 中弥补 UL84 的缺失。

Guinea pig cytomegalovirus GP84 is a functional homolog of the human cytomegalovirus (HCMV) UL84 gene that can complement for the loss of UL84 in a chimeric HCMV.

机构信息

Center for Infectious Diseases and Microbiology, Translational Research and Division of Infectious Diseases, University of Minnesota Medical School, Department of Pediatrics, 2001 Sixth Street SE, Minneapolis, MN 55455, USA.

出版信息

Virology. 2011 Feb 5;410(1):76-87. doi: 10.1016/j.virol.2010.10.028. Epub 2010 Nov 20.

Abstract

The guinea pig cytomegalovirus (GPCMV) co-linear gene and potential functional homolog of HCMV UL84 (GP84) was investigated. The GP84 gene had delayed early transcription kinetics and transient expression studies of GP84 protein (pGP84) demonstrated that it targeted the nucleus and co-localized with the viral DNA polymerase accessory protein as described for HCMV pUL84. Additionally, pGP84 exhibited a transdominant inhibitory effect on viral growth as described for HCMV. The inhibitory domain could be localized to a minimal peptide sequence of 99 aa. Knockout of GP84 generated virus with greatly impaired growth kinetics. Lastly, the GP84 ORF was capable of complementing for the loss of the UL84 coding sequence in a chimeric HCMV. Based on this research and previous studies we conclude that GPCMV is similar to HCMV by encoding single copy co-linear functional homologs of HCMV UL82 (pp71), UL83 (pp65) and UL84 genes.

摘要

研究了豚鼠巨细胞病毒(GPCMV)与 HCMV UL84(GP84)共线性基因和潜在的功能同源物。GP84 基因具有延迟的早期转录动力学,并且对 GP84 蛋白(pGP84)的瞬时表达研究表明,它靶向核,并与病毒 DNA 聚合酶辅助蛋白共定位,如 HCMV pUL84 所述。此外,如 HCMV 所述,pGP84 对病毒生长表现出显性抑制作用。抑制结构域可以定位于 99 个氨基酸的最小肽序列。GP84 的敲除产生了生长动力学大大受损的病毒。最后,GP84 ORF 能够在嵌合 HCMV 中弥补 UL84 编码序列的缺失。基于这项研究和以前的研究,我们得出结论,GPCMV 通过编码 HCMV UL82(pp71)、UL83(pp65)和 UL84 基因的单拷贝共线性功能同源物,与 HCMV 相似。

相似文献

3
Sequence and transcriptional analysis of the guinea pig cytomegalovirus UL97 homolog.
Virus Genes. 1997;15(3):255-64. doi: 10.1023/a:1007988705909.
7
Characteristics of Immediate-Early 2 (IE2) and UL84 Proteins in UL84-Independent Strains of Human Cytomegalovirus (HCMV).
Microbiol Spectr. 2021 Oct 31;9(2):e0053921. doi: 10.1128/Spectrum.00539-21. Epub 2021 Sep 22.
9
Molecular characterization of the guinea pig cytomegalovirus UL83 (pp65) protein homolog.
Virus Genes. 1999;19(3):205-21. doi: 10.1023/a:1008136714136.
10
Characterization of a cluster of late genes of guinea pig cytomegalovirus.
Virus Genes. 2001 Dec;23(3):247-56. doi: 10.1023/a:1012536804190.

引用本文的文献

7
Guinea pig cytomegalovirus trimer complex gH/gL/gO uses PDGFRA as universal receptor for cell fusion and entry.
Virology. 2020 Sep;548:236-249. doi: 10.1016/j.virol.2020.05.012. Epub 2020 Jun 11.
8
Neutralization of Human Cytomegalovirus Entry into Fibroblasts and Epithelial Cells.
Vaccines (Basel). 2017 Oct 31;5(4):39. doi: 10.3390/vaccines5040039.
10
A Homolog Pentameric Complex Dictates Viral Epithelial Tropism, Pathogenicity and Congenital Infection Rate in Guinea Pig Cytomegalovirus.
PLoS Pathog. 2016 Jul 7;12(7):e1005755. doi: 10.1371/journal.ppat.1005755. eCollection 2016 Jul.

本文引用的文献

1
Current and new cytomegalovirus antivirals and novel animal model strategies.
Inflamm Allergy Drug Targets. 2010 Sep;9(4):286-99. doi: 10.2174/187152810793358822.
4
The design, structures and therapeutic potential of protein epitope mimetics.
Drug Discov Today. 2008 Nov;13(21-22):944-51. doi: 10.1016/j.drudis.2008.07.008. Epub 2008 Sep 11.
5
Cytomegalovirus UL97 mutations in the era of ganciclovir and maribavir.
Rev Med Virol. 2008 Jul-Aug;18(4):233-46. doi: 10.1002/rmv.574.
9
Pivotal role of animal models in the development of new therapies for cytomegalovirus infections.
Antiviral Res. 2006 Sep;71(2-3):164-71. doi: 10.1016/j.antiviral.2006.05.018. Epub 2006 Jun 19.
10
Antiviral drugs for cytomegalovirus diseases.
Antiviral Res. 2006 Sep;71(2-3):154-63. doi: 10.1016/j.antiviral.2006.05.002. Epub 2006 May 23.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验