Rm. Wright et al., CLONING AND CHARACTERIZATION OF THE GENE CODING FOR THE HUMAN ACROSOMAL PROTEIN SP-10, Biology of reproduction, 49(2), 1993, pp. 316-325
SP-10 is a human intra-acrosomal protein that is first detected in the
developing acrosome of round spermatids and is observed associated wi
th the acrosomal membranes and matrix of mature sperm. Recombinant SP-
10 is currently being tested as a contraceptive vaccine immunogen on t
he basis of its tissue specificity as well as functional assays indica
ting that anti-SP-10 antisera inhibit sperm-egg interactions. In the p
resent study, structural characterization of the human SP-10 gene was
undertaken to investigate the expression of the gene and to identify p
ossible functions of the SP-10 protein within the acrosome. Genomic bl
ots indicate that SP-10 is encoded by a single-copy gene. Mapping and
sequencing of the 8-kb SP-10 gene show that the SP-10 mRNA consists of
exons of 119, 487, 113, and 390 bp with each exon coding for a distin
ct structural domain within the SP-10 protein. An in-frame alternative
ly spliced form of the SP-10 mRNA, identified during SP-10 cDNA charac
terization, employs the same 3' splice site as the 487-bp exon and a u
nique 5' splice site within the 487-bp exon. Previous comparisons of h
uman, baboon, and macaque SP-10 cDNA sequences indicated that the babo
on and macaque cDNAs contained 60 bp (20 aa) not present in the human
SP-10 cDNA. Analysis of the human SP-10 genomic sequence suggests that
a 60-bp deletion may have occurred during the evolution of the human
SP-10 gene by homologous recombination. This deletion may be responsib
le for the reduced level of alternatively spliced SP-10 message presen
t within the human testis.