Functional characterisation of mutations in the ligand-binding domain of the androgen receptor gene in patients with androgen insensitivity syndrome

Five mutations in the ligand-binding domain of the androgen receptor gene w ere identified in patients with complete (A765T, C784Y, R831X and M895T) or partial (R840G) androgen insensitivity. A765T and R831X have been reported previously whereas the other three mutations are novel. Receptors carrying these mutations were transiently expressed in COS-1 cells, and androgen bi nding and capacity to transactivate an androgen-responsive reporter gene we re assayed. C784Y led to abolished androgen. binding and transactivating ca pacity, R840G and M895T showed reduced specific binding and partial transac tivation. The in vitro functions of the R840G and M895T mutants were improv ed with supraphysiological concentrations of steroid.