The sex determining gene SRY was screened for molecular alteration in
an XY sex reversed female by single-strand conformation polymorphism (
SSCP) technique, An A-to G transition was detected which leads to an e
xchange of a tyrosine by a cysteine in the SRY protein. The affected t
yrosine residue located at the C terminus of the DNA binding protein i
s evolutionarily strongly conserved among the members of the HMG box c
ontaining proteins. Using gel shift assay and peptide synthesis such a
mutation is shown to abolish the SRY protein DNA binding ability. The
involvement of this particular amino acid in the binding specificity
is also discussed. (C) 1994 Wiley-Liss, Inc.