Molecular Cloning, Expression, and Mapping of the High Affinity Actin-Capping Domain of Chicken Cardiac Tensin

• Published in: The Journal of cell biology Vol. 128; no. 6; pp. 1095 - 1109
• Main Authors: Chuang, Jen-Zen, Lin, Diane C., Lin, Shin
• Format: Journal Article
• Language: English
• Published: United States Rockefeller University Press 01.03.1995; The Rockefeller University Press
• Subjects: 3T3 Cells; Actins; Actins - chemistry; Amino Acid Sequence; Amino acids; Animals; Base Sequence; Cell Line; Cells; Cellular biology; Chickens; Cloning, Molecular; Complementary DNA; Deoxyribonucleic acid; DNA; Gizzard; Heart; Humans; Kidney cells; Mice; Microfilament Proteins - biosynthesis; Microfilament Proteins - genetics; Microfilament Proteins - isolation & purification; Microfilaments; Molecular Sequence Data; Myocardium - chemistry; Pests; Polymerization; Poultry; Protein Binding; Proteins; Repetitive Sequences, Nucleic Acid; Sequence Homology; Tensins
• ISSN: 0021-9525; 1540-8140
• DOI: 10.1083/jcb.128.6.1095

Tensin, an actin filament capping protein first purified from chicken gizzard, is localized to various types of adherens junctions in muscle and non-muscle cells. In this paper, we describe the isolation and sequencing of tensin cDNA from a chicken cardiac library. The 6.3-kb chicken cardiac tensin cDNA encodes an open reading frame of 1,792 amino acids. Mammalian cells transfected with the chicken tensin cDNA expressed a polypeptide of ∼200 kD recognizable by antibodies to chicken gizzard tensin. The expressed protein was incorporated into focal adhesions and other actin-containing structures in the transfected cells. To map the domain associated with tensin's high affinity, barbed-end F-actin-capping activity, bacterially expressed recombinant fusion proteins containing various segments of tensin were prepared and assayed for activity. The results of these experiments show that the high affinity capping domain (kD = 1-3 nM) lies within amino acid residues R1037-V1169. Additional studies on a shorter construct, S1061-H1145, showed that these 85 residues were sufficient for producing complete inhibition of actin polymerization and depolymerization. While this active domain is located within that of the "insertin" sequence (Weigt, C., A. Gaertner, A. Wegner, H. Korte, and H. E. Meyer. 1992. J. Mol. Biol. 227:593-595), our data showing complete inhibition of polymerization and shift in critical concentration are consistent with a simple barbed-end capping mechanism rather than the "insertin model." Our results also differ from those of a recent report (Lo, S. H., P. A. Janmey, J. H. Hartwig, and L. B. Chen. 1994. J. Cell Biol. 125:1067-1075), which concluded that their recombinant tensin has an "insertin-like" inhibitory effect on barbed-end actin polymerization, and that this activity is attributed to residues T936-R1037 (residues 888-989 in their numbering system). In our study, a fusion construct (N790-K1060) encompassing T936-R1037 had no significant effect on actin polymerization and depolymerization, even at high concentrations.