Transgenic expression constructs were employed to identify a cis-acting transcription element in the T cell receptor (TCR)-γ locus, called HsA, between the Vγ5 and Vγ2 genes. In constructs lacking the previously defined enhancer (3′ECγ1), HsA supports transcription in mature but not immature T cells in a largely position-independent fashion. 3′ECγ1, without HsA, supports transcription in immature and mature T cells but is subject to severe position effects. Together, the two elements support expression in immature and mature T cells in a copy number–dependent, position-independent fashion. Furthermore, HsA was necessary for consistent rearrangement of transgenic recombination substrates. These data suggest that HsA provides chromatin-opening activity and, together with 3′ECγ1, constitutes a T cell–specific locus control region for the TCR-γ locus.
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6 September 1999
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September 06 1999
A Novel Element Upstream of the Vγ2 Gene in the Murine T Cell Receptor γ Locus Cooperates with the 3′ Enhancer to Act as a Locus Control Region
Jeanne E. Baker,
Jeanne E. Baker
aFrom the Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720
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Joonsoo Kang,
Joonsoo Kang
aFrom the Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720
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Na Xiong,
Na Xiong
aFrom the Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720
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Tempe Chen,
Tempe Chen
aFrom the Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720
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Dragana Cado,
Dragana Cado
aFrom the Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720
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David H. Raulet
David H. Raulet
aFrom the Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720
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Jeanne E. Baker
aFrom the Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720
Joonsoo Kang
aFrom the Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720
Na Xiong
aFrom the Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720
Tempe Chen
aFrom the Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720
Dragana Cado
aFrom the Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720
David H. Raulet
aFrom the Department of Molecular and Cell Biology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, California 94720
1used in this paper: DN, double-negative; DP, double-positive; LCR, locus control region; rr, rearranged; RT, reverse transcriptase; SP, single-positive
Received:
March 17 1999
Revision Requested:
June 21 1999
Accepted:
June 28 1999
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 1999 The Rockefeller University Press
1999
The Rockefeller University Press
J Exp Med (1999) 190 (5): 669–680.
Article history
Received:
March 17 1999
Revision Requested:
June 21 1999
Accepted:
June 28 1999
Citation
Jeanne E. Baker, Joonsoo Kang, Na Xiong, Tempe Chen, Dragana Cado, David H. Raulet; A Novel Element Upstream of the Vγ2 Gene in the Murine T Cell Receptor γ Locus Cooperates with the 3′ Enhancer to Act as a Locus Control Region. J Exp Med 6 September 1999; 190 (5): 669–680. doi: https://doi.org/10.1084/jem.190.5.669
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