Patterns of p53, p73 and mortalin gene expression associated with haemocyte polyploidy in the soft-shell clam, Mya arenaria |
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Authors: | Siah A Delaporte M Pariseau J McKenna P Berthe F C J |
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Affiliation: | a University of Prince Edward Island, Atlantic Veterinary College, Department of Pathology and Microbiology, Charlottetown, C1A 4P3, Prince Edward Island, Canada b Institut des sciences de la mer de Rimouski (ISMER), 310, allée des Ursulines, C.P. 3300 Rimouski (Québec) Canada G5L 3A1 c Animal Health and Welfare, European Food Safety Authority, EFSA, Largo N. Palli 5/A, I-43100 Parma, Italy d Université Louis Pasteur, Institut de Virologie, 3 rue Koeberlé, 67000 Strasbourg, France |
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Abstract: | The molecular mechanisms by which haemocytes of clams are transformed in the course of haemic neoplasia remain by far unknown. The aim of this study was to quantify the expression of p53/p73 and mortalin genes, in relation with the ploidy status of clam haemocytes and to correlate the p53 expression with mortalin expression. For this purpose, soft-shell clams, Mya arenaria, were collected from an endemic zone for neoplasia. The ploidy of haemocytes was assessed for each individual clam by flow cytometry using a propidium iodide protocol, while p53/p73 and mortalin gene expressions were quantified by real-time RT-PCR. Results show that haemocytes of some clams with a moderate percentage (15-50%) of tetraploid cells have a significantly high level of p53 and p73 in comparison with clams belonging to categories with low (<15%) or high levels (>50%) of tetraploid cells, where low levels of expression of these genes were observed. Furthermore, mortalin gene expression is strongly correlated (r2 = 0.68, p < 0.01) with p53 gene expression level. This reinforces the hypothesis of a cytoplasmic p53 sequestration mechanism in clam haemic neoplasia. Further studies are needed to confirm these preliminary results and further unravel the molecular pathways involved in this process. Our results are believed to provide phenotypic foundation for such studies to be undertaken. |
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Keywords: | Mya arenaria Haemocytes p53 p73 Mortalin Tetraploidy |
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