Literature DB >> 19955333

Pronounced segregation of donor mitochondria introduced by bovine ooplasmic transfer to the female germ-line.

Christina Ramires Ferreira1, Jörg Patrick Burgstaller, Felipe Perecin, Joaquim Mansano Garcia, Marcos Roberto Chiaratti, Simone Cristina Méo, Mathias Müller, Lawrence Charles Smith, Flávio Vieira Meirelles, Ralf Steinborn.   

Abstract

Ooplasmic transfer (OT) has been used in basic mouse research for studying the segregation of mtDNA, as well as in human assisted reproduction for improving embryo development in cases of persistent developmental failure. Using cattle as a large-animal model, we demonstrate that the moderate amount of mitochondria introduced by OT is transmitted to the offspring's oocytes; e.g., modifies the germ line. The donor mtDNA was detectable in 25% and 65% of oocytes collected from two females. Its high variation in heteroplasmic oocytes, ranging from 1.1% to 33.5% and from 0.4% to 15.5%, can be explained by random genetic drift in the female germ line. Centrifugation-mediated enrichment of mitochondria in the pole zone of the recipient zygote's ooplasm and its substitution by donor ooplasm led to elevated proportions of donor mtDNA in reconstructed zygotes compared with zygotes produced by standard OT (23.6% +/- 9.6% versus 12.1% +/- 4.5%; P < 0.0001). We also characterized the proliferation of mitochondria from the OT parents-the recipient zygote (Bos primigenius taurus type) and the donor ooplasm (B. primigenius indicus type). Regression analysis performed for 57 tissue samples collected from the seven OT fetuses at different points during fetal development found a decreasing proportion of donor mtDNA (r(2) = 0.78). This indicates a preferred proliferation of recipient taurine mitochondria in the context of the nuclear genotype of the OT recipient expressing a B. primigenius indicus phenotype.

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Year:  2009        PMID: 19955333     DOI: 10.1095/biolreprod.109.080564

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  14 in total

1.  Comparing four laboratory three-parent techniques to construct human aged non-surrounded nucleolus germinal vesicle oocytes: A case-control study.

Authors:  Sara Darbandi; Mahsa Darbandi; Ashok Agarwal; Hamid Reza Khorram Khorshid; Mohammad Reza Sadeghi; Sandro C Esteves; Pallav Sengupta; Sulagna Dutta; Zohreh Fathi; Hojjat Zeraati; Mohammad Mehdi Akhondi
Journal:  Int J Reprod Biomed       Date:  2020-06-30

Review 2.  Transmission of mitochondrial DNA diseases and ways to prevent them.

Authors:  Joanna Poulton; Marcos R Chiaratti; Flávio V Meirelles; Stephen Kennedy; Dagan Wells; Ian J Holt
Journal:  PLoS Genet       Date:  2010-08-12       Impact factor: 5.917

3.  Real-Time PCR Quantification of Heteroplasmy in a Mouse Model with Mitochondrial DNA of C57BL/6 and NZB/BINJ Strains.

Authors:  Thiago Simões Machado; Carolina Habermann Macabelli; Juliano Rodrigues Sangalli; Thiago Bittencourt Rodrigues; Lawrence Charles Smith; Flávio Vieira Meirelles; Marcos Roberto Chiaratti
Journal:  PLoS One       Date:  2015-08-14       Impact factor: 3.240

Review 4.  Ooplasmic transfer in human oocytes: efficacy and concerns in assisted reproduction.

Authors:  Sara Darbandi; Mahsa Darbandi; Hamid Reza Khorram Khorshid; Mohammad Reza Sadeghi; Ashok Agarwal; Pallav Sengupta; Safaa Al-Hasani; Mohammad Mehdi Akhondi
Journal:  Reprod Biol Endocrinol       Date:  2017-10-02       Impact factor: 5.211

5.  The role of mitochondria from mature oocyte to viable blastocyst.

Authors:  Scott Chappel
Journal:  Obstet Gynecol Int       Date:  2013-05-16

6.  Preimplantation death of xenomitochondrial mouse embryo harbouring bovine mitochondria.

Authors:  Manabu Kawahara; Shiori Koyama; Satomi Iimura; Wataru Yamazaki; Aiko Tanaka; Nanami Kohri; Keisuke Sasaki; Masashi Takahashi
Journal:  Sci Rep       Date:  2015-09-29       Impact factor: 4.379

Review 7.  Mitochondrial DNA disease and developmental implications for reproductive strategies.

Authors:  Joerg Patrick Burgstaller; Iain G Johnston; Joanna Poulton
Journal:  Mol Hum Reprod       Date:  2014-11-24       Impact factor: 4.025

8.  Modulating mitochondrial quality in disease transmission: towards enabling mitochondrial DNA disease carriers to have healthy children.

Authors:  Alan Diot; Eszter Dombi; Tiffany Lodge; Chunyan Liao; Karl Morten; Janet Carver; Dagan Wells; Tim Child; Iain G Johnston; Suzannah Williams; Joanna Poulton
Journal:  Biochem Soc Trans       Date:  2016-08-15       Impact factor: 5.407

9.  Additional mitochondrial DNA influences the interactions between the nuclear and mitochondrial genomes in a bovine embryo model of nuclear transfer.

Authors:  Kanokwan Srirattana; Justin C St John
Journal:  Sci Rep       Date:  2018-05-08       Impact factor: 4.379

10.  MtDNA segregation in heteroplasmic tissues is common in vivo and modulated by haplotype differences and developmental stage.

Authors:  Ralf Steinborn; Gottfried Brem; Joerg Patrick Burgstaller; Iain G Johnston; Nick S Jones; Jana Albrechtová; Thomas Kolbe; Claus Vogl; Andreas Futschik; Corina Mayrhofer; Dieter Klein; Sonja Sabitzer; Mirjam Blattner; Christian Gülly; Joanna Poulton; Thomas Rülicke; Jaroslav Piálek
Journal:  Cell Rep       Date:  2014-06-06       Impact factor: 9.423

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