Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Contrasting Effects of in Vitro Fertilization and Nuclear Transfer on the Expression of mtDNA Replication Factors

View through CrossRef
Abstract Mitochondrial DNA (mtDNA) is normally only inherited through the oocyte. However, nuclear transfer (NT), the fusion of a donor cell with an enucleated oocyte, can transmit both donor cell and recipient oocyte mtDNA. mtDNA replication is under the control of nuclear-encoded replication factors, such as polymerase gamma (POLG) and mitochondrial transcription factor A (TFAM). These are first expressed during late preimplantation embryo development. To account for the persistence of donor cell mtDNA, even when introduced at residual levels (mtDNAR), we hypothesized that POLG and TFAM would be upregulated in intra- and interspecific (ovine–ovine) and intergeneric (caprine–ovine) NT embryos when compared to in vitro fertilized (IVF) embryos. For the intra- and interspecific crosses, PolGA (catalytic subunit), PolGB (accessory subunit), and TFAM mRNA were expressed at the 2-cell stage in both nondepleted (mtDNA+) and mtDNAR embryos with protein being expressed up to the 16-cell stage for POLGA and TFAM. However, at the 16-cell stage, there was significantly more PolGA expression in the mtDNAR embryos compared to their mtDNA+ counterparts. Expression for all three genes first matched IVF embryos at the blastocyst stage. In the intergeneric model, POLG was upregulated during preimplantation development. Although these embryos did not persist further than the 16+-cell stage, significantly more mtDNAR embryos reached this stage. However, the vast majority of these embryos were homoplasmic for recipient oocyte mtDNA. The upreglation in mtDNA replication factors was most likely due to the donor cells still expressing these factors prior to NT.
Title: Contrasting Effects of in Vitro Fertilization and Nuclear Transfer on the Expression of mtDNA Replication Factors
Description:
Abstract Mitochondrial DNA (mtDNA) is normally only inherited through the oocyte.
However, nuclear transfer (NT), the fusion of a donor cell with an enucleated oocyte, can transmit both donor cell and recipient oocyte mtDNA.
mtDNA replication is under the control of nuclear-encoded replication factors, such as polymerase gamma (POLG) and mitochondrial transcription factor A (TFAM).
These are first expressed during late preimplantation embryo development.
To account for the persistence of donor cell mtDNA, even when introduced at residual levels (mtDNAR), we hypothesized that POLG and TFAM would be upregulated in intra- and interspecific (ovine–ovine) and intergeneric (caprine–ovine) NT embryos when compared to in vitro fertilized (IVF) embryos.
For the intra- and interspecific crosses, PolGA (catalytic subunit), PolGB (accessory subunit), and TFAM mRNA were expressed at the 2-cell stage in both nondepleted (mtDNA+) and mtDNAR embryos with protein being expressed up to the 16-cell stage for POLGA and TFAM.
However, at the 16-cell stage, there was significantly more PolGA expression in the mtDNAR embryos compared to their mtDNA+ counterparts.
Expression for all three genes first matched IVF embryos at the blastocyst stage.
In the intergeneric model, POLG was upregulated during preimplantation development.
Although these embryos did not persist further than the 16+-cell stage, significantly more mtDNAR embryos reached this stage.
However, the vast majority of these embryos were homoplasmic for recipient oocyte mtDNA.
The upreglation in mtDNA replication factors was most likely due to the donor cells still expressing these factors prior to NT.

Related Results

The consequences of nuclear transfer for mammalian foetal development and offspring survival. A mitochondrial DNA perspective
The consequences of nuclear transfer for mammalian foetal development and offspring survival. A mitochondrial DNA perspective
The introduction of nuclear transfer (NT) and other technologies that involve embryo reconstruction require us to reinvestigate patterns of mitochondrial DNA (mtDNA) transmission, ...
MitoDelta: identifying mitochondrial DNA deletions at cell-type resolution from single-cell RNA sequencing data
MitoDelta: identifying mitochondrial DNA deletions at cell-type resolution from single-cell RNA sequencing data
AbstractBackgroundDeletion variants in mitochondrial DNA (mtDNA) are associated with various diseases, such as mitochondrial disorders and neurodegenerative diseases. Traditionally...
Effects of different fertilization practices on the N03-N, N, P, K, Ca, Mg, ash and dietary fibre contents of carrot
Effects of different fertilization practices on the N03-N, N, P, K, Ca, Mg, ash and dietary fibre contents of carrot
The effects of different fertilization practices on the NO3-N, N, P, K, Ca, Mg, ash and dietary fibre contents of carrots were studied in field experiments in southern Finland. Uni...
Anti-Müllerian hormone independently affect mtDNA copy number in human granulosa cells
Anti-Müllerian hormone independently affect mtDNA copy number in human granulosa cells
Abstract Background: Recently, as a delayed childbearing trend is emerging in modern women’s adulthood, diminished reproductive potential due to age...
CpG methylation patterns of human mitochondrial DNA
CpG methylation patterns of human mitochondrial DNA
AbstractThe epigenetic modification of mitochondrial DNA (mtDNA) is still in controversy. To clarify this point, we applied the gold standard method for DNA methylation, bisulfite ...
Mitochondrial DNA variation across 56,434 individuals in gnomAD
Mitochondrial DNA variation across 56,434 individuals in gnomAD
ABSTRACTDatabases of allele frequency are extremely helpful for evaluating clinical variants of unknown significance; however, until now, genetic databases such as the Genome Aggre...

Back to Top