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PMID: 3681192 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Sequence analysis and expression of an X-linked, lymphocyte-regulated gene family (XLR).

The Journal of experimental medicine ·Vol. 166 ·No. 6 ·1987-12-01 ·Pages 1702-15

Siegel JN, Turner CA, Klinman DM, Wilkinson M, Steinberg AD, MacLeod CL, Paul WE, Davis MM, Cohen DI

Abstract

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.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Cell Differentiation Cloning, Molecular DNA/genetics Gene Expression Regulation Immunologic Deficiency Syndromes/genetics Intermediate Filament Proteins/genetics Lamins Lymphocytes/physiology Mice Molecular Sequence Data Multigene Family Nuclear Proteins/genetics X Chromosome
Chemicals
Intermediate Filament Proteins Lamins Nuclear Proteins DNA
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Siegel J N
Laboratory of Chemical Biology, National Institute of Diabetes, and Digestive and Kidney Diseases, Bethesda, Maryland 20892.
Turner C A
Klinman D M
Wilkinson M
Steinberg A D
MacLeod C L
Paul W E
Davis M M
Cohen D I
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1987-12-01
Pages
1702-15
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2188785
Subset
IM
Grants
NIAID NIH HHS · AI-20320 · United States
NCI NIH HHS · CA-37778 · United States
PHS HHS · T32-H107107 · United States
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