Title of article :
T cell activation induces a noncoding RNA transcript sensitive to inhibition by immunosuppressant drugs and encoded by the proto-oncogene, BIC
Author/Authors :
Haasch، نويسنده , , Deanna and Chen، نويسنده , , Yung-Wu and Reilly، نويسنده , , Regina M and Grace Chiou، نويسنده , , X and Koterski، نويسنده , , Sandra J. Smith، نويسنده , , Morey L and Kroeger، نويسنده , , Paul and McWeeny، نويسنده , , Kerri and Halbert، نويسنده , , Donald N and Mollison، نويسنده , , Karl W and Djuric، نويسنده , , Stevan W and Trevillyan، نويسنده , , James M، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2002
Pages :
9
From page :
78
To page :
86
Abstract :
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 BIC proto-oncogene that encodes a noncoding mRNA (W. Tam, Gene 274 (2001) 157). Our data demonstrate that transcriptional activation of the BIC proto-oncogene is an early and sustained T cell activation event and suggest an important role for noncoding mRNA in T cell function.
Keywords :
Noncoding RNA , Proto-Oncogene , activation , Immunosuppressant drug , T cell
Journal title :
Cellular Immunology
Serial Year :
2002
Journal title :
Cellular Immunology
Record number :
1847180
Link To Document :
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