Function of cGMP-dependent protein kinases as revealed by gene deletion

F Hofmann, R Feil, T Kleppisch… - Physiological …, 2006 - journals.physiology.org
F Hofmann, R Feil, T Kleppisch, J Schlossmann
Physiological reviews, 2006journals.physiology.org
Over the past few years, a wealth of biochemical and functional data have been gathered on
mammalian cGMP-dependent protein kinases (cGKs). In mammals, three different kinases
are encoded by two genes. Mutant and chimeric cGK proteins generated by molecular
biology techniques yielded important biochemical knowledge, such as the function of the
NH2-terminal domains of cGKI and cGKII, the identity of the cGMP-binding sites of cGKI, and
the substrate specificity of the enzymes. Genetic approaches have proven especially useful …
Over the past few years, a wealth of biochemical and functional data have been gathered on mammalian cGMP-dependent protein kinases (cGKs). In mammals, three different kinases are encoded by two genes. Mutant and chimeric cGK proteins generated by molecular biology techniques yielded important biochemical knowledge, such as the function of the NH2-terminal domains of cGKI and cGKII, the identity of the cGMP-binding sites of cGKI, and the substrate specificity of the enzymes. Genetic approaches have proven especially useful for the analysis of the biological functions of cGKs. Recently, some of the in vivo targets and mechanisms leading to changes in neuronal adaptation, smooth muscle relaxation and growth, intestinal water secretion, bone growth, renin secretion, and other important functions have been identified. These data show that cGKs are signaling molecules involved in many biological functions.
American Physiological Society