摘要
During liquefaction of the ejaculate, the semen coagulum proteins semenogelin I （SEMG1） and semenogelin Ⅱ （SEMG2） are degraded to low molecular mass fragments by kallikrein-related peptidase 3 （KLK3）, also known as prostate-specific antigen. Semenogelin molecules initiate their own destruction by chelating Zn^2＋ that normally would completely inhibit the proteolytic activity of KLK3. In a similar way, semenogelins might regulate the activity of kallikrein-related peptidases in the epididymis, something that might be of importance for the maturation of spermatozoa or generation of anti-bacterial peptides. Studies on the evolution of semen coagulum proteins have revealed that most of them carry an exon that displays a rapid and unusual evolution. As a consequence, homologous proteins in rodents and primates show almost no conservation in primary structure. Further studies on their evolution suggest that the progenitor of the semen coagulum proteins probably was a protease inhibitor that might have displayed antimicrobial activity. The semenogelin locus on chromosome 20 contains at least 17 homologous genes encoding probable protease inhibitors with homology to semen coagulum proteins. All of these are highly expressed in the epididymis where they, similar to the semenogelins, could affect the maturation of spermatozoa or display antibacterial properties. （Asian J Androl 2007 July; 9： 540-544）
During liquefaction of the ejaculate, the semen coagulum proteins semenogelin I （SEMG1） and semenogelin Ⅱ （SEMG2） are degraded to low molecular mass fragments by kallikrein-related peptidase 3 （KLK3）, also known as prostate-specific antigen. Semenogelin molecules initiate their own destruction by chelating Zn^2＋ that normally would completely inhibit the proteolytic activity of KLK3. In a similar way, semenogelins might regulate the activity of kallikrein-related peptidases in the epididymis, something that might be of importance for the maturation of spermatozoa or generation of anti-bacterial peptides. Studies on the evolution of semen coagulum proteins have revealed that most of them carry an exon that displays a rapid and unusual evolution. As a consequence, homologous proteins in rodents and primates show almost no conservation in primary structure. Further studies on their evolution suggest that the progenitor of the semen coagulum proteins probably was a protease inhibitor that might have displayed antimicrobial activity. The semenogelin locus on chromosome 20 contains at least 17 homologous genes encoding probable protease inhibitors with homology to semen coagulum proteins. All of these are highly expressed in the epididymis where they, similar to the semenogelins, could affect the maturation of spermatozoa or display antibacterial properties. （Asian J Androl 2007 July; 9： 540-544）
