Epigenetic and non-epigenetic mode of SIRT1 action during oocyte meiosis progression.

Epigenetics Histone code In vitro maturation Oocyte SIRT1 Sirtuin 1

Journal

Journal of animal science and biotechnology
ISSN: 1674-9782
Titre abrégé: J Anim Sci Biotechnol
Pays: England
ID NLM: 101581293

Informations de publication

Date de publication:
2019
Historique:
received: 04 01 2019
accepted: 11 06 2019
entrez: 16 8 2019
pubmed: 16 8 2019
medline: 16 8 2019
Statut: epublish

Résumé

SIRT1 histone deacetylase acts on many epigenetic and non-epigenetic targets. It is thought that SIRT1 is involved in oocyte maturation; therefore, the importance of the ooplasmic SIRT1 pool for the further fate of mature oocytes has been strongly suggested. We hypothesised that SIRT1 plays the role of a signalling molecule in mature oocytes through selected epigenetic and non-epigenetic regulation. We observed SIRT1 re-localisation in mature oocytes and its association with spindle microtubules. In mature oocytes, SIRT1 distribution shows a spindle-like pattern, and spindle-specific SIRT1 action decreases α-tubulin acetylation. Based on the observation of the histone code in immature and mature oocytes, we suggest that SIRT1 is mostly predestined for an epigenetic mode of action in the germinal vesicles (GVs) of immature oocytes. Accordingly, BML-278-driven trimethylation of lysine K9 in histone H3 in mature oocytes is considered to be a result of GV epigenetic transformation. Taken together, our observations point out the dual spatiotemporal SIRT1 action in oocytes, which can be readily switched from the epigenetic to non-epigenetic mode of action depending on the progress of meiosis.

Sections du résumé

BACKGROUND BACKGROUND
SIRT1 histone deacetylase acts on many epigenetic and non-epigenetic targets. It is thought that SIRT1 is involved in oocyte maturation; therefore, the importance of the ooplasmic SIRT1 pool for the further fate of mature oocytes has been strongly suggested. We hypothesised that SIRT1 plays the role of a signalling molecule in mature oocytes through selected epigenetic and non-epigenetic regulation.
RESULTS RESULTS
We observed SIRT1 re-localisation in mature oocytes and its association with spindle microtubules. In mature oocytes, SIRT1 distribution shows a spindle-like pattern, and spindle-specific SIRT1 action decreases α-tubulin acetylation. Based on the observation of the histone code in immature and mature oocytes, we suggest that SIRT1 is mostly predestined for an epigenetic mode of action in the germinal vesicles (GVs) of immature oocytes. Accordingly, BML-278-driven trimethylation of lysine K9 in histone H3 in mature oocytes is considered to be a result of GV epigenetic transformation.
CONCLUSIONS CONCLUSIONS
Taken together, our observations point out the dual spatiotemporal SIRT1 action in oocytes, which can be readily switched from the epigenetic to non-epigenetic mode of action depending on the progress of meiosis.

Identifiants

pubmed: 31413827
doi: 10.1186/s40104-019-0372-3
pii: 372
pmc: PMC6688279
doi:

Types de publication

Journal Article

Langues

eng

Pagination

67

Déclaration de conflit d'intérêts

Competing interestsThe authors declare that they have no competing interests.

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Auteurs

Jan Nevoral (J)

1Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, 323 00 Pilsen, Czech Republic.
2Department of Histology and Embryology, Faculty of Medicine in Pilsen, Charles University, Karlovarska 48, 301 66 Pilsen, Czech Republic.

Lukas Landsmann (L)

1Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, 323 00 Pilsen, Czech Republic.
3Faculty of Science, Charles University, Albertov 2038/6, 128 00 Prague, Czech Republic.

Miriam Stiavnicka (M)

1Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, 323 00 Pilsen, Czech Republic.

Petr Hosek (P)

1Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, 323 00 Pilsen, Czech Republic.

Jiri Moravec (J)

1Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, 323 00 Pilsen, Czech Republic.

Sarka Prokesova (S)

1Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, 323 00 Pilsen, Czech Republic.
4Faculty of Agriculture, Food and Natural Resources, Czech University of Life Sciences in Prague, Kamycka 129, 165 00 Praha-Suchdol, Czech Republic.
5Institute of Animal Science, Pratelstvi 815/107, 104 00, Prague 10-Uhrineves, Czech Republic.

Hedvika Rimnacova (H)

1Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, 323 00 Pilsen, Czech Republic.

Eliska Koutna (E)

1Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, 323 00 Pilsen, Czech Republic.
4Faculty of Agriculture, Food and Natural Resources, Czech University of Life Sciences in Prague, Kamycka 129, 165 00 Praha-Suchdol, Czech Republic.

Pavel Klein (P)

1Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, 323 00 Pilsen, Czech Republic.

Kristyna Hoskova (K)

5Institute of Animal Science, Pratelstvi 815/107, 104 00, Prague 10-Uhrineves, Czech Republic.

Tereza Zalmanova (T)

5Institute of Animal Science, Pratelstvi 815/107, 104 00, Prague 10-Uhrineves, Czech Republic.

Tereza Fenclova (T)

1Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, 323 00 Pilsen, Czech Republic.

Jaroslav Petr (J)

5Institute of Animal Science, Pratelstvi 815/107, 104 00, Prague 10-Uhrineves, Czech Republic.

Milena Kralickova (M)

1Biomedical Center, Faculty of Medicine in Pilsen, Charles University, alej Svobody 1655/76, 323 00 Pilsen, Czech Republic.
2Department of Histology and Embryology, Faculty of Medicine in Pilsen, Charles University, Karlovarska 48, 301 66 Pilsen, Czech Republic.

Classifications MeSH