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Printable Handouts
Navigable Slide Index
- Introduction
- Symbiotic origins of mitochondria in our cells
- Mitochondria - lungs of the cell
- Human mitochondrial DNA
- High copy number per cell
- mtDNA disease
- Maternal inheritance of mitochondria
- Cases of paternal inheritance of mtDNA?
- Lower effective population size
- Fast mutation rate
- Mutation rate estimation
- Natural variation of mitochondrial genomes
- Haplotypes and haplogroups (1)
- Haplotypes and haplogroups (2)
- Three distinct migrations to the Americans
- mtDNA haplogroup distribution map
- The hierarchy of human population structure
- Geographic distribution of variation
- Geographic diversity of mt DNA variation
- Natural selection and adaptation to climate?
- Old and young clades
- Low levels of human mtDNA variation?
- Models for modern human origins
- What tree patterns are predicted?
- Evidence for hybridization?
- Archaic vs. modern human DNA
- Complex ancestry of human origins
- Nested structure of mtDNA haplogroups
- Marital residence and genetic diversity
- The effect of matriolocal residence on diversity
- Were ancient Austronesians matrilocal?
- Haplogroup B4a1a variation
- Austronesian origins
- The genetic landscape of Europe
- Homogenous mtDNA pool of Europe
- Changes in ancient mtDNA pool of Europe (1)
- Changes in ancient mtDNA pool of Europe (2)
- Summary
Topics Covered
- Origins of mitochondria in our cells
- Functional role, size, and copy number of mitochondria
- Inheritance of mitochondrial genes
- Mitochondrial mutation rate
- Haplotypes and haplogroups
- Geographic distribution of mtDNA diversity in humans
- Natural selection and dispersals in shaping mtDNA variation
- Residence pattern effect on mtDNA diversity
Links
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Talk Citation
Kivisild, T. (2021, January 31). Evolution of human mitochondrial DNA variations [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/QVNX1681.Export Citation (RIS)
Publication History
Financial Disclosures
- Toomas Kivisild has no commercial/financial relationships to disclose.
A selection of talks on Biochemistry
Transcript
Please wait while the transcript is being prepared...
0:00
Hello. My name is Toomas Kivisild and I'm
a human geneticist working in the Department of Human Genetics at KU Leuven.
This talk is about evolution of human mitochondrial DNA variation.
0:17
To talk about the origin of mitochondria in our cells,
we need to go back in time more than
two billion years to the origin of life on Earth,
and the first split into two major domains,
the bacteria and the archaea.
It is only after these two domains had evolved that
our eukaryotic origins emerged as a merger between the archaea and the bacteria.
We have inherited our nuclear genes predominantly from our archaeal ancestors,
and we have got our mitochondria from
a specific branch of the bacteria, the alpha purple bacteria,
so that our cells contain these two distinct forms of life.
The mitochondria in our cells are very important.
They're important for the energetic purposes of our cells,
and they have enabled the eukaryotic organisms to diversify in cell type and cell size.
During these two billion years since the origins of eukaryotes,
there has been an ongoing process of transfer of mitochondrial genes to the nucleus.
As a reminder of these two distinct origins,
there are differences in the code.
For example, in the mitochondrial DNA,
the TGA codon means tryptophan,
whereas in the nuclear language it means a stop code.
When we look at each cell of a eukaryote,