𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Microarray analyses of differentially expressed human genes and biological processes in ECV304 cells infected with rubella virus

✍ Scribed by Xiao-yang Mo; Wenli Ma; Yali Zhang; Haiquan Zhao; Yun Deng; Wuzhou Yuan; Yuequn Wang; Yongqin Li; Chuanbing Zhu; Mingyao Liu; Xiushan Wu


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
132 KB
Volume
79
Category
Article
ISSN
0146-6615

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Changes in mRNA expression levels of ECV304 cells infected with the wild‐type rubella strain were analyzed using a microarray system representing 18,716 human genes. Four hundred eighty‐seven genes exhibited differential expression levels; 456 of these genes were up‐regulated while 31 genes were down‐regulated. We identified 53 biological processes that were significantly relevant to the RV‐infection. Among these biological processes, 52 were one‐gene processes and one was a process involving five genes: IFNA21 (interferon, alpha 21), interferon stimulated exonuclease gene 20 kDa (ISG20), zinc finger protein 175 (ZNF175), tripartite motif‐containing 22 (TRIM22), and MX2 [myxovirus (influenza virus) resistance 2 (mouse)]. Except for ZNF175, gene annotation indicated four of these genes encoded interferon or interferon‐induced genes. These results suggest that genes relevant to interferon‐regulated pathways may be involved in the pathogenesis of rubella. J. Med. Virol. 79:1783–1791, 2007. © 2007 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Differential display RT-PCR analysis of
✍ Kingsley J.L. Liew; Vincent T.K. Chow 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 248 KB 👁 1 views

## Abstract Differential display (DD)‐RT‐PCR was employed to analyze mRNAs from ECV304 human endothelial‐like cells undergoing apoptosis following infection with the virulent New Guinea C strain of dengue virus type 2 in order to elucidate the cellular gene responses to dengue viral infection at th

Validation and application of normalizat
✍ S. Chey; C. Claus; U.G. Liebert 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 355 KB

## Abstract Reference genes are generally employed in real‐time quantitative PCR (RT‐qPCR) experiments to normalize variability between different samples. The aim of this study was to identify and validate appropriate reference genes as internal controls for RT‐qPCR experiments in rubella virus (RV