EsturgeonV1, PubMed, Corpus, bibRecord, 000276

Comparison of protein fractions in seminal plasma from multiple sperm collections in sterlet (Acipenser ruthenus).

Identifieur interne : 000276 ( PubMed/Corpus ); précédent : 000275; suivant : 000277

Comparison of protein fractions in seminal plasma from multiple sperm collections in sterlet (Acipenser ruthenus).

Auteurs : A. Shaliutina ; M. Hulak ; P. Li ; M. Sulc ; B. Dzyuba ; O. Linhart

Source :

Reproduction in domestic animals = Zuchthygiene [ 1439-0531 ] ; 2013.

RBID : pubmed:22747924

English descriptors

KwdEn :
- Animals, Electrophoresis, Polyacrylamide Gel, Fish Proteins (physiology), Fishes (physiology), Gene Expression Regulation (physiology), Male, Semen (physiology), Spermatozoa (physiology), Time Factors.
MESH :
- chemical , physiology : Fish Proteins.
- physiology : Fishes, Gene Expression Regulation, Semen, Spermatozoa.
- Animals, Electrophoresis, Polyacrylamide Gel, Male, Time Factors.

Abstract

Seminal plasma of sterlet Acipenser ruthenus was evaluated using comparative proteomics to characterize its protein fractions and to determine any influence of multiple sperm collections on these proteins. An experimental group of fish was used, in which sperm was collected three times at 5 h intervals. Protein fractions of seminal plasma were determined by SDS-gel electrophoresis (SDS-PAGE) and two-dimensional electrophoresis high-resolution gels (2D). At all stripping times, five protein bands with molecular weights of 93, 53, 48, 33 and 28 kDa were identified using SDS-PAGE. No significant differences (p > 0.05) in relative mass of protein bands among collections were observed. At the third collection, 20 protein spots were detected from the two-dimensional gels, compared to 17 found at the first and second collections. Ten protein spots, from the third stripping, were analysed. Screening of these spots by mass spectrometric analysis showed positive results for spot 10. Direct comparison across public databases revealed sequence similarity with two hypothetical proteins, MCAG_00854 and IscW_ISCW011489. Differences in the seminal plasma protein fractions were found at the third stripping compared to the first two. It is hypothesized that these extra proteins after the third collection could be involved in some step of intracellular mechanism which is responsible for regulating of spermatozoa motility. However, protein identification revealed no significant distinction for any protein spot and protein sequences available in public databases. These results highlighted the need for a complete genome sequences for sturgeons.

DOI: 10.1111/j.1439-0531.2012.02118.x
PubMed: 22747924

Links to Exploration step

pubmed:22747924

Le document en format XML

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<author><name sortKey="Shaliutina, A" sort="Shaliutina, A" uniqKey="Shaliutina A" first="A" last="Shaliutina">A. Shaliutina</name>
<affiliation><nlm:affiliation>Faculty of Fisheries and Protection of Waters, South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, University of South Bohemia in Ceske Budejovice, Vodnany, Czech Republic.</nlm:affiliation>
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<author><name sortKey="Hulak, M" sort="Hulak, M" uniqKey="Hulak M" first="M" last="Hulak">M. Hulak</name>
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<author><name sortKey="Li, P" sort="Li, P" uniqKey="Li P" first="P" last="Li">P. Li</name>
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<author><name sortKey="Sulc, M" sort="Sulc, M" uniqKey="Sulc M" first="M" last="Sulc">M. Sulc</name>
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<author><name sortKey="Dzyuba, B" sort="Dzyuba, B" uniqKey="Dzyuba B" first="B" last="Dzyuba">B. Dzyuba</name>
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<author><name sortKey="Linhart, O" sort="Linhart, O" uniqKey="Linhart O" first="O" last="Linhart">O. Linhart</name>
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<author><name sortKey="Sulc, M" sort="Sulc, M" uniqKey="Sulc M" first="M" last="Sulc">M. Sulc</name>
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<author><name sortKey="Dzyuba, B" sort="Dzyuba, B" uniqKey="Dzyuba B" first="B" last="Dzyuba">B. Dzyuba</name>
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<front><div type="abstract" xml:lang="en">Seminal plasma of sterlet Acipenser ruthenus was evaluated using comparative proteomics to characterize its protein fractions and to determine any influence of multiple sperm collections on these proteins. An experimental group of fish was used, in which sperm was collected three times at 5 h intervals. Protein fractions of seminal plasma were determined by SDS-gel electrophoresis (SDS-PAGE) and two-dimensional electrophoresis high-resolution gels (2D). At all stripping times, five protein bands with molecular weights of 93, 53, 48, 33 and 28 kDa were identified using SDS-PAGE. No significant differences (p > 0.05) in relative mass of protein bands among collections were observed. At the third collection, 20 protein spots were detected from the two-dimensional gels, compared to 17 found at the first and second collections. Ten protein spots, from the third stripping, were analysed. Screening of these spots by mass spectrometric analysis showed positive results for spot 10. Direct comparison across public databases revealed sequence similarity with two hypothetical proteins, MCAG_00854 and IscW_ISCW011489. Differences in the seminal plasma protein fractions were found at the third stripping compared to the first two. It is hypothesized that these extra proteins after the third collection could be involved in some step of intracellular mechanism which is responsible for regulating of spermatozoa motility. However, protein identification revealed no significant distinction for any protein spot and protein sequences available in public databases. These results highlighted the need for a complete genome sequences for sturgeons.</div>
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<Title>Reproduction in domestic animals = Zuchthygiene</Title>
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<ArticleTitle>Comparison of protein fractions in seminal plasma from multiple sperm collections in sterlet (Acipenser ruthenus).</ArticleTitle>
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<Abstract><AbstractText>Seminal plasma of sterlet Acipenser ruthenus was evaluated using comparative proteomics to characterize its protein fractions and to determine any influence of multiple sperm collections on these proteins. An experimental group of fish was used, in which sperm was collected three times at 5 h intervals. Protein fractions of seminal plasma were determined by SDS-gel electrophoresis (SDS-PAGE) and two-dimensional electrophoresis high-resolution gels (2D). At all stripping times, five protein bands with molecular weights of 93, 53, 48, 33 and 28 kDa were identified using SDS-PAGE. No significant differences (p > 0.05) in relative mass of protein bands among collections were observed. At the third collection, 20 protein spots were detected from the two-dimensional gels, compared to 17 found at the first and second collections. Ten protein spots, from the third stripping, were analysed. Screening of these spots by mass spectrometric analysis showed positive results for spot 10. Direct comparison across public databases revealed sequence similarity with two hypothetical proteins, MCAG_00854 and IscW_ISCW011489. Differences in the seminal plasma protein fractions were found at the third stripping compared to the first two. It is hypothesized that these extra proteins after the third collection could be involved in some step of intracellular mechanism which is responsible for regulating of spermatozoa motility. However, protein identification revealed no significant distinction for any protein spot and protein sequences available in public databases. These results highlighted the need for a complete genome sequences for sturgeons.</AbstractText>
<CopyrightInformation>© 2012 Blackwell Verlag GmbH.</CopyrightInformation>
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Comparison of protein fractions in seminal plasma from multiple sperm collections in sterlet (Acipenser ruthenus).

Comparison of protein fractions in seminal plasma from multiple sperm collections in sterlet (Acipenser ruthenus).

Source :

English descriptors

Abstract

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki