Gene cloning of rat and mouse platelet glycoprotein V: identification of megakaryocyte-specific promoters and demonstration of functional thrombin cleavage
| Autor: | C, Ravanat, M, Morales, D O, Azorsa, S, Moog, S, Schuhler, P, Grunert, D, Loew, A, Van Dorsselaer, J P, Cazenave, F, Lanza |
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| Rok vydání: | 1997 |
| Předmět: |
Mice
Inbred BALB C Base Sequence Sequence Homology Amino Acid Molecular Sequence Data Restriction Mapping Thrombin Exons Introns Peptide Fragments Recombinant Proteins Cell Line Rats Mice Platelet Glycoprotein GPIb-IX Complex Sequence Homology Nucleic Acid Animals Humans Female Amino Acid Sequence Cloning Molecular Rats Wistar Promoter Regions Genetic Megakaryocytes Conserved Sequence |
| Zdroj: | Blood. 89(9) |
| ISSN: | 0006-4971 |
| Popis: | Platelet glycoprotein (GP) V is a major surface protein cleaved during thrombin-induced platelet activation. GPV associates noncovalently with the GPIb-IX complex to form GPIb-V-IX, a receptor for von Willebrand factor and thrombin. We describe the cloning of the genes coding for rat and mouse GPV and compare them with the human gene. The two rodent genes have a similar structure and resemble the human GPV gene with a coding sequence (approximately 1,700 nucleotides) entirely contained in one exon and a single intron (approximately 900 nucleotides) in the 5' untranslated region. Both genes have megakaryocyte-type promoters with conserved tandem Ets and GATA recognition motifs and lack a TATA box. The mature rat and mouse proteins comprise 551 amino acids, have 70% sequence identity, and contain an additional 8-amino acid intracellular segment as compared with the human protein. As in human GPV, there is an NH2-terminal leucine-rich region of 15 repeats and a thrombin cleavage recognition sequence. Whereas the rat and human thrombin cleavage sites are similar, the mouse cleavage site resembles that of the human thrombin receptor. Functionality of these sites was demonstrated by thrombin cleavage of synthetic peptides and analysis by high-performance liquid chromatography (HPLC) or mass spectrometry. Cleavage of native rat GPV was confirmed by means of a polyclonal antibody directed against the new NH2-terminal peptide exposed after thrombin cleavage. This antibody specifically recognized thrombin-activated rat platelets by fluorescence-activated cell sorting (FACS) analysis. In addition, we raised monoclonal antibodies specific for rat GPV (88 kD), which recognized the NH2-terminal soluble fragment (70 kD) liberated after thrombin cleavage. Knowledge of these rodent GPV genes and availability of species-specific peptides and antibodies will be essential to further studies aiming to define the exact in vivo function of platelet GPV using animal models of thrombosis and gene inactivation experiments. |
| Databáze: | OpenAIRE |
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