NDLI: Cloning from the thyroid of a protein related to actin binding protein that is recognized by Graves disease immunoglobulins.

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Cloning from the thyroid of a protein related to actin binding protein that is recognized by Graves disease immunoglobulins.

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	O'brien, E. Leedman, P. J. Harrison, P. J. Faulkner-jones, B. West, J. Coppel, R. L. Cram, D. S. Simpson, R. Harrison, L. C.
Description	Author Affiliation: Leedman PJ ( Burnet Clinical Research Unit, Walter and Eliza Hall Institute of Medical Research, Victoria, Australia.);
Abstract	Human actin binding protein (ABP) links specific membrane glycoproteins to cytoskeletal actin microfilaments. In human platelets and leukocytes, ABP directly links, respectively, the membrane glycoproteins GPIb and the high-affinity Fc receptor for IgG (Fc gamma IR) to cytoskeletal actin microfilaments. Similar interaction between the thyrotropin (TSH) receptor and ABP in endocrine cells might explain the rapid and profound disruption of actin microfilaments induced by TSH in cultured thyroid follicular cells. By screening a thyroid lambda gt11 cDNA expression library with serum from a Graves disease patient, we identified a clone encoding a protein, designated truncated ABP (TABP), that shares extensive homology (approximately 70%) with ABP. TABP is a truncated ABP-like protein with an open reading frame of 195 aa that encodes a protein of approximately 21 kDa. TABP lacks an actin binding domain but contains two predicted beta-sheet repeats within which is a putative dimerization domain and between which lies a putative glycoprotein binding site containing a consensus site for phosphorylation by Ca(2+)-calmodulin kinase II. TABP contains a unique C-terminal insertion within which lies a hydrophobic predicted membrane-associated region, absent from ABP. Although TABP mRNA is expressed widely, immunoblot analysis demonstrated the presence of TABP antibodies specifically in the sera of a minority of subjects with autoimmune thyroid disease. A 24-residue sequence of similarity was identified between the TSH receptor and platelet glycoprotein GPIb alpha that may represent a transmembrane ABP binding site. We suggest, therefore, that signal transduction by TSH in the thyroid involves direct linkage of the TSH receptor to actin microfilaments by ABP and that TABP may interact with ABP to mediate TSH-induced actin microfilament disruption.
ISSN	00278424
e-ISSN	10916490
Journal	Proceedings of the National Academy of Sciences of the United States of America
Issue Number	13
Volume Number	90
Language	English
Publisher	National Academy of Sciences
Publisher Date	1993-08-01
Publisher Place	United States
Access Restriction	Open
Subject Keyword	Cloning, Molecular Graves Disease Immunology Immunoglobulins Microfilament Proteins Genetics Thyroid Gland Chemistry Amino Acid Sequence Animals Mice Physiology Molecular Sequence Data RNA, Messenger Receptors, Thyrotropin Recombinant Fusion Proteins Sequence Homology, Amino Acid Signal Transduction Research Support, Non-U.S. Gov't Multidisciplinary
Content Type	Text
Resource Type	Article
Subject	Multidisciplinary

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