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The activity and copy number of mitochondrial DNA in ovine oocytes throughout oogenesis in vivo and during oocyte maturation in vitro

Mitochondria are responsible for the production of ATP, which drives cellular metabolic and biosynthetic processes. This is the first study to quantify the mtDNA copy number across all stages of oogenesis in a large monovulatory species, it includes assessment of the activity of mitochondria in germ...

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Autores principales: Cotterill, Matthew, Harris, Sarah E., Collado Fernandez, Esther, Lu, Jianping, Huntriss, John D., Campbell, Bruce K., Picton, Helen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3690804/
https://www.ncbi.nlm.nih.gov/pubmed/23468533
http://dx.doi.org/10.1093/molehr/gat013
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author Cotterill, Matthew
Harris, Sarah E.
Collado Fernandez, Esther
Lu, Jianping
Huntriss, John D.
Campbell, Bruce K.
Picton, Helen M.
author_facet Cotterill, Matthew
Harris, Sarah E.
Collado Fernandez, Esther
Lu, Jianping
Huntriss, John D.
Campbell, Bruce K.
Picton, Helen M.
author_sort Cotterill, Matthew
collection PubMed
description Mitochondria are responsible for the production of ATP, which drives cellular metabolic and biosynthetic processes. This is the first study to quantify the mtDNA copy number across all stages of oogenesis in a large monovulatory species, it includes assessment of the activity of mitochondria in germinal vesicle (GV) and metaphase II (MII) oocytes through JC1 staining. Primordial to early antral follicles (n = 249) were isolated from the sheep ovarian cortex following digestion at 37°C for 1 h and all oocytes were disaggregated from their somatic cells. Germinal vesicle oocytes (n = 133) were aspirated from 3- to 5-mm diameter antral follicles, and mature MII oocytes (n = 71) were generated following in vitro maturation (IVM). The mtDNA copy number in each oocyte was quantified using real-time PCR and showed a progressive, but variable increase in the amount of mtDNA in oocytes from primordial follicles (605 ± 205, n = 8) to mature MII oocytes (744 633 ± 115 799, n = 13; P < 0.05). Mitochondrial activity (P > 0.05) was not altered during meiotic progression from GV to MII during IVM. The observed increase in the mtDNA copy number across oogenesis reflects the changing ATP demands needed to orchestrate cytoskeletal and cytoplasmic reorganization during oocyte growth and maturation and the need to fuel the resumption of meiosis in mature oocytes following the pre-ovulatory gonadotrophin surge.
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spelling pubmed-36908042013-06-24 The activity and copy number of mitochondrial DNA in ovine oocytes throughout oogenesis in vivo and during oocyte maturation in vitro Cotterill, Matthew Harris, Sarah E. Collado Fernandez, Esther Lu, Jianping Huntriss, John D. Campbell, Bruce K. Picton, Helen M. Mol Hum Reprod Articles Mitochondria are responsible for the production of ATP, which drives cellular metabolic and biosynthetic processes. This is the first study to quantify the mtDNA copy number across all stages of oogenesis in a large monovulatory species, it includes assessment of the activity of mitochondria in germinal vesicle (GV) and metaphase II (MII) oocytes through JC1 staining. Primordial to early antral follicles (n = 249) were isolated from the sheep ovarian cortex following digestion at 37°C for 1 h and all oocytes were disaggregated from their somatic cells. Germinal vesicle oocytes (n = 133) were aspirated from 3- to 5-mm diameter antral follicles, and mature MII oocytes (n = 71) were generated following in vitro maturation (IVM). The mtDNA copy number in each oocyte was quantified using real-time PCR and showed a progressive, but variable increase in the amount of mtDNA in oocytes from primordial follicles (605 ± 205, n = 8) to mature MII oocytes (744 633 ± 115 799, n = 13; P < 0.05). Mitochondrial activity (P > 0.05) was not altered during meiotic progression from GV to MII during IVM. The observed increase in the mtDNA copy number across oogenesis reflects the changing ATP demands needed to orchestrate cytoskeletal and cytoplasmic reorganization during oocyte growth and maturation and the need to fuel the resumption of meiosis in mature oocytes following the pre-ovulatory gonadotrophin surge. Oxford University Press 2013-07 2013-03-05 /pmc/articles/PMC3690804/ /pubmed/23468533 http://dx.doi.org/10.1093/molehr/gat013 Text en © The Author 2013. Published by Oxford University Press on behalf of European Society of Human Reproduction and Embryology. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Articles
Cotterill, Matthew
Harris, Sarah E.
Collado Fernandez, Esther
Lu, Jianping
Huntriss, John D.
Campbell, Bruce K.
Picton, Helen M.
The activity and copy number of mitochondrial DNA in ovine oocytes throughout oogenesis in vivo and during oocyte maturation in vitro
title The activity and copy number of mitochondrial DNA in ovine oocytes throughout oogenesis in vivo and during oocyte maturation in vitro
title_full The activity and copy number of mitochondrial DNA in ovine oocytes throughout oogenesis in vivo and during oocyte maturation in vitro
title_fullStr The activity and copy number of mitochondrial DNA in ovine oocytes throughout oogenesis in vivo and during oocyte maturation in vitro
title_full_unstemmed The activity and copy number of mitochondrial DNA in ovine oocytes throughout oogenesis in vivo and during oocyte maturation in vitro
title_short The activity and copy number of mitochondrial DNA in ovine oocytes throughout oogenesis in vivo and during oocyte maturation in vitro
title_sort activity and copy number of mitochondrial dna in ovine oocytes throughout oogenesis in vivo and during oocyte maturation in vitro
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3690804/
https://www.ncbi.nlm.nih.gov/pubmed/23468533
http://dx.doi.org/10.1093/molehr/gat013
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