TY - JOUR
T1 - Identification of a T-cell-specific enhancer at the locus encoding T-cell antigen receptor γ chain
AU - Kappes, DJ
AU - Browne, CP
AU - Tonegawa, S
PY - 1991/3
Y1 - 1991/3
N2 - The γδ and αβ T-cell antigen receptor (TCR) heterodimers are expressed in a lineage-specific, mutually exclusive manner. Regulation of expression occurs at the transcriptional level. A 13-kilobase (kb) stretch of DNA encompassing variable-joining-constant segments V
γ4-J
γ1-Cγ1 of the murine y-chain gene was examined for the presence of transcriptional enhancing elements by a transient transfection assay. DNA fragments from this region were inserted into a test plasmid containing a heterologous promoter fused to the human growth hormone gene. An 1800-base-pair (bp) fragment located 3 kb 3′ to Cγ exon III was found to display enhancing activity in several T-cell lines. Maximum enhancing activity could be localized further to fragments as small as 400 bp in some cell lines. Nucleotide sequence analysis of this 400-bp segment revealed homologies to previously described core enhancer elements and to other TCR gene enhancers. The TCR γ-chain gene enhancer is active in both γδ and αβ T cells, indicating that it is not primarily responsible for lineagespecificity of expression, but it is inactive in non-T-cells.
AB - The γδ and αβ T-cell antigen receptor (TCR) heterodimers are expressed in a lineage-specific, mutually exclusive manner. Regulation of expression occurs at the transcriptional level. A 13-kilobase (kb) stretch of DNA encompassing variable-joining-constant segments V
γ4-J
γ1-Cγ1 of the murine y-chain gene was examined for the presence of transcriptional enhancing elements by a transient transfection assay. DNA fragments from this region were inserted into a test plasmid containing a heterologous promoter fused to the human growth hormone gene. An 1800-base-pair (bp) fragment located 3 kb 3′ to Cγ exon III was found to display enhancing activity in several T-cell lines. Maximum enhancing activity could be localized further to fragments as small as 400 bp in some cell lines. Nucleotide sequence analysis of this 400-bp segment revealed homologies to previously described core enhancer elements and to other TCR gene enhancers. The TCR γ-chain gene enhancer is active in both γδ and αβ T cells, indicating that it is not primarily responsible for lineagespecificity of expression, but it is inactive in non-T-cells.
KW - Animals
KW - Base Sequence
KW - Enhancer Elements, Genetic
KW - Macromolecular Substances
KW - Mice
KW - Molecular Sequence Data
KW - Plasmids
KW - Receptors, Antigen, T-Cell/genetics
KW - Repetitive Sequences, Nucleic Acid
KW - Restriction Mapping
KW - Sequence Homology, Nucleic Acid
KW - T-Lymphocytes/immunology
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:A1991FC21600036&DestLinkType=FullRecord&DestApp=WOS
UR - http://www.scopus.com/inward/record.url?scp=0026015901&partnerID=8YFLogxK
U2 - 10.1073/pnas.88.6.2204
DO - 10.1073/pnas.88.6.2204
M3 - Article
C2 - 2006158
SN - 0027-8424
VL - 88
SP - 2204
EP - 2208
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 6
ER -