Cloning of sgk serine-threonine protein kinase from shark rectal gland–a gene induced by hypertonicity and secretagogues

S Waldegger, P Barth, JN Forrest Jr, R Greger, F Lang - Pflügers Archiv, 1998 - Springer
S Waldegger, P Barth, JN Forrest Jr, R Greger, F Lang
Pflügers Archiv, 1998Springer
Recently, the cell-volume-regulated serine-threonine protein kinase h-sgk was cloned from
a human hepatoma cell line. The sgk gene was shown to be induced by cell shrinkage in
many different mammalian cell lines. In this study, two highly conserved serine-threonine
protein kinases, sgk-1 and sgk-2, were cloned from rectal gland tissue of the spiny dogfish
(Squalus acanthias). Both kinases showed a distinct pattern of tissue specificity, with high
expression levels in kidney, intestine, liver and heart. In rectal gland slices sgk-1 …
Abstract
 Recently, the cell-volume-regulated serine-threonine protein kinase h-sgk was cloned from a human hepatoma cell line. The sgk gene was shown to be induced by cell shrinkage in many different mammalian cell lines. In this study, two highly conserved serine-threonine protein kinases, sgk-1 and sgk-2, were cloned from rectal gland tissue of the spiny dogfish (Squalus acanthias). Both kinases showed a distinct pattern of tissue specificity, with high expression levels in kidney, intestine, liver and heart. In rectal gland slices sgk-1 transcription was induced by exposure to hypertonic solution, reduction of the extracellular urea concentration, and addition of the secretagogues vasoactive intestinal polypeptide (VIP) and carbachol. The shark sgk-1 serine-threonine protein kinase may therefore provide a link between cell volume, Clsecretion and protein phosphorylation state in shark rectal gland cells.
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