Abstract
Gene expression for calbindin‐D28k, the 28,000 relative molecular mass vitamin D‐dependent calcium‐binding protein, was measured in cells of the murine nephron by in situ hybridization on tissue sections (hybridization cytochemistry). Radiolabeled (35S‐UTP), single‐stranded RNA complementary to calbinding‐D28k‐mRNA (probe RNA) was prepared from linearized cDNA template and used for the hybridizations. Autoradiography was carried out and cellular levels of hybridization signal (silver grains) were quantified. After corretion for background the concentration of silver grains was more than 350% greater in the distal tubule than in either the proximal tubule or the glomerulus. The relative cellular level of mRNA in the cytoplasm, as reflected in silver grains/cell, of the distal tubules with probe RNA was 3.4 times greater than that with control RNA. Cells of the distal tubule were the only apparent sites of specific hybridization with probe RNA. The presence of calbindin‐D28k‐mRNA in the distal tubule corresponded to the localizations of calbindin‐D28k by immunocytochemistry.