A partial cDNA sequence of the boar 28, 29-kDa proacrosin-binding protein w
as determined. The desired sequence was amplified and obtained by RT-PCR fo
llowed by nested PCR. The oligonucleotide primers for RT-PCR were designed
by deduction from the internal amino acid sequence of the boar proacrosin-b
inding protein. An approximately 1-kbp DNA fragment was analysed by agarose
gel electrophoresis, in which the boar testicular total RNA or poly(A)(+)
RNA was used as a template for RT-PCR followed by nested PCR. This PCR prod
uct was inserted into a TA vector. The DNA sequence of the inserted PCR pro
duct was then determined by the chain termination method.