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
相关论文
共 32 条
[1]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[2]   PROTEINS REGULATING RAS AND ITS RELATIVES [J].
BOGUSKI, MS ;
MCCORMICK, F .
NATURE, 1993, 366 (6456) :643-654
[3]   A DIFFERENTIAL MOLECULAR-BIOLOGY SEARCH FOR GENES PREFERENTIALLY EXPRESSED IN FUNCTIONAL LYMPHOCYTES-T - THE CTLA GENES [J].
BRUNET, JF ;
DENIZOT, F ;
GOLSTEIN, P .
IMMUNOLOGICAL REVIEWS, 1988, 103 :21-36
[4]   Identification of a putative G protein-coupled receptor induced during activation-induced apoptosis of T cells [J].
Choi, JW ;
Lee, SY ;
Choi, YW .
CELLULAR IMMUNOLOGY, 1996, 168 (01) :78-84
[5]   CONTINGENT GENETIC REGULATORY EVENTS IN LYMPHOCYTE-T ACTIVATION [J].
CRABTREE, GR .
SCIENCE, 1989, 243 (4889) :355-361
[6]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[7]   Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells [J].
Elbashir, SM ;
Harborth, J ;
Lendeckel, W ;
Yalcin, A ;
Weber, K ;
Tuschl, T .
NATURE, 2001, 411 (6836) :494-498
[8]   ISOLATION OF CDNA CLONES ENCODING T-CELL-SPECIFIC MEMBRANE-ASSOCIATED PROTEINS [J].
HEDRICK, SM ;
COHEN, DI ;
NIELSEN, EA ;
DAVIS, MM .
NATURE, 1984, 308 (5955) :149-153
[9]   GTPases in antigen receptor signalling [J].
Henning, SW ;
Cantrell, DA .
CURRENT OPINION IN IMMUNOLOGY, 1998, 10 (03) :322-329
[10]   Functional discovery via a compendium of expression profiles [J].
Hughes, TR ;
Marton, MJ ;
Jones, AR ;
Roberts, CJ ;
Stoughton, R ;
Armour, CD ;
Bennett, HA ;
Coffey, E ;
Dai, HY ;
He, YDD ;
Kidd, MJ ;
King, AM ;
Meyer, MR ;
Slade, D ;
Lum, PY ;
Stepaniants, SB ;
Shoemaker, DD ;
Gachotte, D ;
Chakraburtty, K ;
Simon, J ;
Bard, M ;
Friend, SH .
CELL, 2000, 102 (01) :109-126