By Michael Bader, Michael Kaling (auth.), Klaus Lindpaintner, Detlev Ganten (eds.)

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Large open arrows indicate hydrolysis site of prorenin In vivo that leads to activation (note that this differs for rat because rat prorenin has a lysine instead of an arginine at the activation site used in the other species). Small arrows indicate subsequent site of cleavage of at least some of the mature renin to give active two-chain renin (this differs for the human protein and the two chains produced are not held together by disulphide bridges, -5-5-, as in the mouse and rat protein). The question mark at the rat signal peptide cleavage site (and the range of values for amino acids in rat pre- and profragments) indicates that several possible Fiydrolysis sites have been suggested but none as yet established.

Sou brier F, Panthier J-j, Corvol P, Rougeon F: Molecular cloning and nucleotide sequence of a human renin eDNA fragment. Nucleic Acids Res 1983, 11:7181-7190. 26. 27. 28. 29. 30. 31. 32. 33. 34. 35. 36. 37. 38. 39. 40. 41. 42. 43. 44. 45. Aldred GP, Fu P, Crawford R], Fernley RT: The sequence and tissue expression of ovine renin. J Mol Endocrinol 1992, 8:3-11. Morris BI: New possibilities for intracellular renin and inactive renin now that the structure of the human renin gene has been elucidated (editorial).

68. 69. Dzau VI. Brody T, Ellison KE, Pratt RE, Ingelfinger JR: Tissuespecific regulation of renin expression in the mouse. Hyperrension 1987, 9 (suppl 111):11136-11141. : Androgen dependence and tissue specificity of renin messenger RNA expression in mice. J Hypertens 1990, 8:45-52. Deschepper CF, Mellon SH, Cumin F, Baxter JD, Ganong WF: Analysis by immunocytochemisty and in situ hybridization of renin and its mRNA in kidney, testis, adrenal, and pituitary of the rat. Proc Narl Acad Sci USA 1986, 83:7552-7556.

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