The catalytic subunits of Na
+, K
+-ATPase were isolated from the kidney and brain of rats (α I and α II, respectively). The antisera raised against these subunits were used as probes to analyze the isoforms of catalytic subunits of Na
+, K
+-ATPase in various tissues of rats. The submandibular gland (SMG) contained a new α subunit isoform (designated α (S) in this report) in addition to α I identical to those found in the kidney and brain. The new α (S) strongly cross-reacted with anti-α I -antiserum. The α (S) had a molecular weight slightly less (approximately 90 kDa) than the kidney and brainα I. The author examined whether or not the α (S) is formed by proteolytic cleavage of α subunits and concluded that this is not the case. The α (S) reacted with [γ-
32P] ATP, resulting in the formation of radioactive α subunit which was stabilized by 2 mM ouabain but which was labile in the presence of 70mM potassium chloride. The author detected only a single species of mRNA for the α subunit in the rat SMG. The Ki value of the submandibular gland Na
+, K
+-ATPase on the ouabain was similar to that of the kidney. The N-terminal amino acid sequence of the α (S) corresponded with that of the α I. In conclusion, the author suggested that, at first the α I was synthesized with the α I mRNA, secondly the α (S) appeared after the C-terminal of the α I was processed in the rat SMG
in vivo.
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