T lymphocyte activation gene identification by coregulated expression on DNA microarrays

被引:64
作者
Mao, M [1 ]
Biery, MC [1 ]
Kobayashi, SV [1 ]
Ward, T [1 ]
Schimmack, G [1 ]
Burchard, J [1 ]
Schelter, JM [1 ]
Dai, HY [1 ]
He, YDD [1 ]
Linsley, PS [1 ]
机构
[1] Rosetta Inpharmat LLC, Merck Res Labs, Seattle, WA 98109 USA
关键词
microarray; T cell; activation; coregulation;
D O I
10.1016/j.ygeno.2003.12.019
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
High-capacity methods for assessing gene function have become increasingly important because of the increasing number of newly identified genes emerging from large-scale genome sequencing and cDNA cloning efforts. We investigated the use of DNA microarrays to identify uncharacterized genes specifically involved in human T cell activation. Activation of human peripheral blood T lymphocytes induced significant changes in hundreds of transcripts, but most of these were not unique to T cell activation. Variation of experimental parameters and analysis techniques allowed better enrichment for gene expression changes unique to T cell activation. Best results were achieved by identification of genes that were most highly coregulated with the T-cell-specific transcript interleukin 2 (IL2) in a "compendium" of experiments involving both T cells and other cell types. Among the genes most highly coregulated with IL2 were many genes known to function during T cell activation, together with ESTs of unknown function. Four of these ESTs were extended to novel full-length clones encoding T-cell-regulated proteins with predicted functions in GTP metabolism, cell organization, and signal transduction. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:989 / 999
页数:11
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