Label-free protein quantification in freshly ejaculated versus post-mating spermatophores of the noble crayfish Astacus astacus
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25871631
DOI
10.1016/j.jprot.2015.04.004
PII: S1874-3919(15)00165-7
Knihovny.cz E-zdroje
- Klíčová slova
- Alpha-2-macroglobulin, Hemocyanin, Histone, Ryanodine receptor, Sodium/hydrogen exchanger, Spermatozoon capacitation,
- MeSH
- alfa-makroglobuliny metabolismus MeSH
- chromatografie kapalinová MeSH
- hemokyanin metabolismus MeSH
- histony metabolismus MeSH
- hmotnostní spektrometrie MeSH
- kapacitace spermií MeSH
- Na(+)-H(+) antiport metabolismus MeSH
- proteomika metody MeSH
- ryanodinový receptor vápníkového kanálu metabolismus MeSH
- severní raci fyziologie MeSH
- sexuální faktory MeSH
- spermatogonie fyziologie MeSH
- spermie fyziologie MeSH
- upregulace MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- alfa-makroglobuliny MeSH
- hemokyanin MeSH
- histony MeSH
- Na(+)-H(+) antiport MeSH
- ryanodinový receptor vápníkového kanálu MeSH
UNLABELLED: Crayfish spermatophores are deposited on the body surface of the female during mating and remain there for a period of time before fertilization ensues. Post-mating changes in protein expression level in the noble crayfish Astacus astacus spermatophore were quantified. In-gel digestion and high resolution mass spectrometry were used for label-free protein quantification. One hundred twelve proteins were identified in the spermatophore of noble crayfish. After 7 days of storage on the body of the female, 6 proteins were identified in the post-mating spermatophore that showed significant up-regulation and 4 significant down-regulations (p < 0.05, fold change ≥ 2). The highest rate of up-regulation was observed in sodium/hydrogen exchanger, which may indicate the importance of intracellular pH adjustment for final maturation of the crayfish spermatozoon. The highest rate of down-regulation was observed in histone H2A. This may increase chromatin flexibility and facilitate its transfer into the oocyte during fertilization. The vitellogenin protein was identified in the crayfish spermatophore and its level changed during storage on the body surface of female. Extensive proteomic modification of male gametes during storage on the body surface of the female suggests post-mating final maturation of the crayfish spermatozoon. BIOLOGICAL SIGNIFICANCE: Freshwater crayfish comprise a large and diverse group of ecologically and commercially important animals. Molecular studies of gametes in the crayfish can provide insight into the complex process of reproduction in this diverse group of animals. The results of such studies can be used for development of new techniques for artificial reproduction of these economically important species.
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