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PMID: 7829530 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Identification of Rlk, a novel protein tyrosine kinase with predominant expression in the T cell lineage.

The Journal of biological chemistry ·Vol. 270 ·No. 4 ·1995-01-27 ·Pages 1928-34

Hu Q, Davidson D, Schwartzberg PL, Macchiarini F, Lenardo MJ, Bluestone JA, Matis LA

Abstract

The control of phosphorylation by protein tyrosine kinases represents an important regulatory mechanism in T cell growth, function, and differentiation. We have identified a 62-kDa murine protein tyrosine kinase predominantly expressed within the T cell lineage, which we have termed Rlk (for Resting lymphocyte kinase). rlk mRNA was found to be expressed in the fetal thymus as early as day 13 of embryonic development as well as in adult thymus and mature resting peripheral T cells. The sequence of rlk showed that it is most closely related to the subfamily of cytoplasmic tyrosine kinases that includes the Btk, Itk, and Tec proteins. However, Rlk differs from these kinases by virtue of its unique aminoterminal domain, which lacks a region of pleckstrin homology common to the other members of this protein subfamily. Examination of rlk abundance within different T cell subpopulations revealed preferential expression in Th1 relative to Th2 T cell clones, suggesting a possible role in signal transduction pathways that selectively regulate cytokine production in mature CD4+ T cell subsets. Rlk thus represents a novel cytoplasmic tyrosine kinase with potential functions in intrathymic T cell development and mature T cell signaling.

Related Genes
rlk
MeSH Terms
Amino Acid Sequence Animals Base Sequence Cell Line Cloning, Molecular Conserved Sequence DNA Primers Humans Mice Molecular Sequence Data Organ Specificity Peptides/chemical synthesis,pharmacology Phosphorylation Protein-Tyrosine Kinases/biosynthesis,chemistry,metabolism Recombinant Proteins/biosynthesis,metabolism Restriction Mapping Sequence Homology, Amino Acid T-Lymphocytes/enzymology Tumor Cells, Cultured
Chemicals
DNA Primers Peptides Recombinant Proteins Tec protein-tyrosine kinase Protein-Tyrosine Kinases
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Hu Q
Immunobiology Program, Alexion Pharmaceuticals, Inc., New Haven, Connecticut 06511.
Davidson D
Schwartzberg P L
Macchiarini F
Lenardo M J
Bluestone J A
Matis L A
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1995-01-27
Pages
1928-34
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIDDK NIH HHS · DK07011 · United States
Databases
GENBANK
L35268
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