دورية أكاديمية

Regulated mitochondrial DNA replication during oocyte maturation is essential for successful porcine embryonic development.

التفاصيل البيبلوغرافية
العنوان: Regulated mitochondrial DNA replication during oocyte maturation is essential for successful porcine embryonic development.
المؤلفون: Spikings, Emma, Alderson, Jon, St John, Justin C.
المساهمون: University of Birmingham
بيانات النشر: Society for the Study of Reproduction
سنة النشر: 2007
المجموعة: University of Bedfordshire Repository
مصطلحات موضوعية: embryo, fertilization, gene regulation, oocyte development, Animals, Blastocyst, Cell Aging, Cells, Cultured, Coloring Agents, DNA Replication, DNA, Mitochondrial, DNA-Directed DNA Polymerase, Embryo Culture Techniques, Embryonic Development, Fertilization in Vitro, Gene Dosage, Immunohistochemistry, Oocytes, Oxazines, RNA, Messenger, Reverse Transcriptase Inhibitors, Reverse Transcriptase Polymerase Chain Reaction, Staining and Labeling, Swine, Time Factors, Transcription Factors, Zalcitabine
الوصف: Cellular ATP is mainly generated through mitochondrial oxidative phosphorylation, which is dependent on mitochondrial DNA (mtDNA). We have previously demonstrated the importance of oocyte mtDNA for porcine and human fertilization. However, the role of nuclear-encoded mitochondrial replication factors during oocyte and embryo development is not yet understood. We have analyzed two key factors, mitochondrial transcription factor A (TFAM) and polymerase gamma (POLG), to determine their role in oocyte and early embryo development. Competent and incompetent oocytes, as determined by brilliant cresyl blue (BCB) dye, were assessed intermittently during the maturation process for TFAM and POLG mRNA using real-time RT-PCR, for TFAM and POLG protein using immunocytochemistry, and for mtDNA copy number using real-time PCR. Analysis was also carried out following treatment of maturing oocytes with the mtDNA replication inhibitor, 2',3'-dideoxycytidine (ddC). Following in vitro fertilization, preimplantation embryos were also analyzed. Despite increased levels of TFAM and POLG mRNA and protein at the four-cell stage, no increase in mtDNA copy number was observed in early preimplantation development. To compensate for this, mtDNA appeared to be replicated during oocyte maturation. However, significant differences in nuclear-encoded regulatory protein expression were observed between BCB(+) and BCB(-) oocytes and between untreated oocytes and those treated with ddC. These changes resulted in delayed mtDNA replication, which correlated to reduced fertilization and embryonic development. We therefore conclude that adherence to the regulation of the timing of mtDNA replication during oocyte maturation is essential for successful embryonic development.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1529-7268
العلاقة: http://www.ncbi.nlm.nih.gov/pubmed/17035641Test; http://www.biolreprod.org/content/76/2/327.longTest; Spikings, E., Alderson, J., St John, J.C. (2007) 'Regulated mitochondrial DNA replication during oocyte maturation is essential for successful porcine embryonic development' Biology of reproduction 76 (2):327-35; http://hdl.handle.net/10547/228294Test; Biology of reproduction
DOI: 10.1095/biolreprod.106.054536
الإتاحة: https://doi.org/10.1095/biolreprod.106.054536Test
http://hdl.handle.net/10547/228294Test
حقوق: Archived with thanks to Biology of reproduction
رقم الانضمام: edsbas.977AFDCE
قاعدة البيانات: BASE
الوصف
تدمد:15297268
DOI:10.1095/biolreprod.106.054536