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Abstract
The ubiquitin-proteasome pathway has been implicated in
the penetration of ascidian vitelline envelope by the
fertilizing spermatozoon (Sawada et al., Proc Natl Acad
Sci U S A 2002; 99:1223-1228). The present study provides
experimental evidence demonstrating proteasome involvement
in the penetration of mammalian zona pellucida (ZP).
Using porcine in vitro fertilization as a model,
penetration of ZP was completely inhibited by specific
proteasomal inhibitors MG-132 and lactacystin. Three
commercial rabbit sera recognizing 20 S proteasomal core
subunits
-1i,
-2i,
-6 and
-5
completely blocked fertilization at a very low
concentration (i.e. diluted 1/2000 to 1/8000 in
fertilization medium). Neither proteasome inhibitors nor
antibodies had any effects on sperm-ZP binding and
acrosome exocytosis in zona-enclosed oocytes or on
fertilization rates in zona-free oocytes, which were
highly polyspermic. Consistent with a possible role of
ubiquitin-proteasome pathway in ZP-penetration, ubiquitin
and various
and
type proteasomal subunits
were detected in boar sperm acrosome by specific
antibodies, immunoprecipitated and microsequenced by
MALDI-TOF from boar sperm extracts.
Anti-ubiquitin-immuno-reactive substrates were detected on
the outer face of ZP by epifluorescence microscopy. This
study therefore provides conclusive evidence implicating
ubiquitin-proteasome pathway in mammalian fertilization
and zona penetration. This finding opens a new line of
acrosome/ZP research since further studies of the sperm
acrosomal proteasome can provide new tools for the
management of polyspermia during in vitro fertilization
and identify new targets for contraceptive development.
Key words:
Gamete Biology
Acrosome reaction
Early development
Fertilization
Sperm
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