The XLR gene family consists of approximately 10 X-linked genes, the expression of which is regulated in lymphocyte development. Certain members of the gene family are closely linked to the murine xid immune deficiency mutation. Sequence analysis of a cDNA clone pM1 derived from the plasmacytoma MOPC167 showed an open reading frame capable of coding for a protein of 208 amino acids and mol wt 24,000. The lack of a signal peptide or transmembrane region indicates a probable cytoplasmic or nuclear localization for the predicted pM1 protein. The predicted protein shares significant homology with lamins A and C and other members of the intermediate filament family of proteins, and shares features important for the coiled-coil structure proposed for these proteins. Analysis of cDNA clones derived from a presecretory lymphoma and from adult thymus indicates that B and T lymphocytes transcribe a common major mRNA identical to pM1, while other rare transcripts were also identified by these studies. A series of clonal T lymphoma lines representing distinct stages of thymic differentiation showed that, as with B lymphoid tumors, XLR expression is correlated with the maturation of the thymomas.
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1 December 1987
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December 01 1987
Sequence analysis and expression of an X-linked, lymphocyte-regulated gene family (XLR).
J N Siegel,
J N Siegel
Laboratory of Chemical Biology, National Institute of Diabetes, and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
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C A Turner,
C A Turner
Laboratory of Chemical Biology, National Institute of Diabetes, and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
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D M Klinman,
D M Klinman
Laboratory of Chemical Biology, National Institute of Diabetes, and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
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M Wilkinson,
M Wilkinson
Laboratory of Chemical Biology, National Institute of Diabetes, and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
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A D Steinberg,
A D Steinberg
Laboratory of Chemical Biology, National Institute of Diabetes, and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
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C L MacLeod,
C L MacLeod
Laboratory of Chemical Biology, National Institute of Diabetes, and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
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W E Paul,
W E Paul
Laboratory of Chemical Biology, National Institute of Diabetes, and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
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M M Davis,
M M Davis
Laboratory of Chemical Biology, National Institute of Diabetes, and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
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D I Cohen
D I Cohen
Laboratory of Chemical Biology, National Institute of Diabetes, and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
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J N Siegel
,
C A Turner
,
D M Klinman
,
M Wilkinson
,
A D Steinberg
,
C L MacLeod
,
W E Paul
,
M M Davis
,
D I Cohen
Laboratory of Chemical Biology, National Institute of Diabetes, and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1987) 166 (6): 1702–1715.
Citation
J N Siegel, C A Turner, D M Klinman, M Wilkinson, A D Steinberg, C L MacLeod, W E Paul, M M Davis, D I Cohen; Sequence analysis and expression of an X-linked, lymphocyte-regulated gene family (XLR).. J Exp Med 1 December 1987; 166 (6): 1702–1715. doi: https://doi.org/10.1084/jem.166.6.1702
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