ITEM METADATA RECORD
Title: Transcriptional regulation of the human CD3 gamma gene: The TATA-less CD3 gamma promoter functions via an initiator and contiguous Sp-binding elements
Authors: Badran, BM ×
Kunstman, K
Stanton, J
Moschitta, M
Zerghe, A
Akl, Haidar
Burny, A
Wolinsky, SM
Willard-Gallo, KE #
Issue Date: May-2005
Publisher: Amer assoc immunologists
Series Title: Journal of Immunology vol:174 issue:10 pages:6238-6249
Abstract: Growing evidence that the CD3γ gene is specifically targeted in some T cell diseases focused our attention on the need to identify and characterize the elusive elements involved in CD3γ transcriptional control. In this study, we show that while the human CD3γ and CD3δ genes are oriented head-to-head and separated by only 1.6 kb, the CD3γ gene is transcribed from an independent but weak, lymphoid-specific TATA-less proximal promoter. Using RNA ligase-mediated rapid amplification of cDNA ends, we demonstrate that a cluster of transcription initiation sites is present in the vicinity of the primary core promoter, and the major start site is situated in a classical initiator sequence. A GT box immediately upstream of the initiator binds Sp family proteins and the general transcription machinery, with the activity of these adjacent elements enhanced by the presence of a second GC box 10 nt further upstream. The primary core promoter is limited to a sequence. that extends upstream to -15 and contains the initiator and GT box. An identical GT box located ∼ 50 nt from the initiator functions as a weak secondary core promoter and likely generates transcripts originating upstream from the +1. Finally, we show that two previously identified NFAT motifs in the proximal promoter positively (NFATγ 1) or negatively (NFATγ(1) and NFATγ(2)) regulate expression of the human CD3γ gene by their differential binding of NFATc1 plus NF-κ B p50 or NFATc2 containing complexes, respectively. These data elucidate some of the mechanisms controlling expression of the CD3γ gene as a step toward furthering our understanding of how its transcription is targeted in human disease.
URI: 
ISSN: 0022-1767
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Laboratory of Molecular and Cellular Signaling
× corresponding author
# (joint) last author

Files in This Item:

There are no files associated with this item.

Request a copy

 




All items in Lirias are protected by copyright, with all rights reserved.

© Web of science