T cell activation induces a noncoding RNA transcript sensitive to inhibition by immunosuppressant drugs and encoded by the proto-oncogene, BIC

被引:162
作者
Haasch, D [1 ]
Chen, YW [1 ]
Reilly, RM [1 ]
Chiou, XG [1 ]
Koterski, S [1 ]
Smith, ML [1 ]
Kroeger, P [1 ]
McWeeny, K [1 ]
Halbert, DN [1 ]
Mollison, KW [1 ]
Djuric, SW [1 ]
Trevillyan, JM [1 ]
机构
[1] Abbott Labs, Global Pharmaceut Res & Dev, Abbott Pk, IL 60064 USA
关键词
noncoding RNA; proto-oncogene; T cell; activation; immunosuppressant drug;
D O I
10.1016/S0008-8749(02)00506-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In a search for novel early T cell activation transcripts, we identified expressed sequence tags (ESTs) more abundantly expressed in normal human CD4(+) T lymphocytes fully activated by a 5 h exposure to CD3 plus CD28 mAbs, compared to the same cells stimulated with either CD3 mAb or CD28 mAb alone. An EST was identified that hybridized with a 1.7 kb transcript expressed in activated T cells but was undetectable by Northern blot analysis in resting T cells or other normal tissues, The T cell transcript was maximally induced within 6 h and remained elevated for at least 47 h. Induction of the transcript was blocked by cyclosporin A, FK506, and dexamethasone but not by rapamycin. The transcript was polyadenylated but lacked an open reading. A BLAST search of the NCBI database revealed that the transcript shared identity with the recently reported human BICproto-oncogene that encodes a noncoding mRNA(W. Tam, Gene 274 (2001) 157). Our data demonstrate that transcriptional activation of the BIC protooncogene is an early and sustained T cell activation event and suggest an important role for noncoding mRNA in T cell function. (C) 2002 Elsevier Science (USA) All rights reserved.
引用
收藏
页码:78 / 86
页数:9
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