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- The Notion of Epigenetics
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1. Cytoplasmic epigenetics: inheritance by cytoplasmic continuity
- Prof. Philippe Silar
- Dr. Fabienne Malagnac
- Epigenetics: Paradigms
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2. The molecular mechanism of X chromosome inactivation
- Prof. Neil Brockdorff
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3. Genomic imprinting: history and embryology
- Prof. Davor Solter
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4. X chromosome inactivation in human cells
- Prof. Barbara Migeon
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5. RNAi and heterochromatin in plants and fission yeast
- Prof. Robert Martienssen
- Epigenetics: Mechanisms
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6. Polycomb epigenetic mechanisms: role of PcG complexes
- Prof. Vincenzo Pirrotta
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7. Polycomb epigenetic mechanisms: methylation of DNA
- Prof. Vincenzo Pirrotta
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8. Histone modifications and prospects for an epigenetic code
- Prof. Bryan Turner
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9. Epigenetic control by histone methylation
- Prof. Thomas Jenuwein
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10. Histone dynamics, heritability and variants
- Dr. Genevieve Almouzni
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11. Gene silencing in budding yeast
- Prof. Susan Gasser
- Epigenetics: Heritability and Reversibility
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12. Nuclear cloning, stem cells and epigenetic reprogramming
- Prof. Rudolf Jaenisch
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13. Stem cell memory
- Prof. James Sherley
- Archived Lectures *These may not cover the latest advances in the field
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14. Epigenetics: a historical overview
- Dr. Robin Holliday
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15. DNA methylation
- Prof. Adrian Bird
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16. DNA methylation and genome defense in Neurospora crassa
- Prof. Eric Selker
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18. Evolution of mammal epigenetic control systems
- Prof. Jenny Graves
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19. Genomic imprinting and its regulation
- Dr. Anne Ferguson-Smith
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20. Nuclear organization and gene expression
- Prof. David Spector
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21. Germ cells
- Prof. Azim Surani
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22. Epigenetic regulation of phenotype
- Prof. Emma Whitelaw
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24. Cytoplasmic epigenetics: proteins acting as genes
- Prof. Reed Wickner
Printable Handouts
Navigable Slide Index
- Introduction
- Talk outline
- Why study human cells?
- Evolution is a tinkerer (1)
- Species differences in dosage compensation
- The Johns Hopkins Hospital
- Dr. Barton Childs
- The Lyon hypothesis
- Davidson, Nitowski and Childs' test of hypothesis
- Results of the study were published in PNAS
- Separating active from inactive X in hybrids
- Comparing active and inactive X
- Cloning the X chromosome
- Differential methylation of the HPRT gene
- CpG islands as control elements
- DNA methylation stabilizes X inactivation
- XIST is a non-coding RNA
- Birdseye view of the XIST locus
- Characteristics of XIST
- Tiny ring Xes that cannot inactivate
- Phenotypes associated with tiny X chromosomes
- How XIST inactivate an X
- The inactive X lacks acetylated histone H4
- Species differences in X inactivation
- Time of onset
- Parental origin of inactive X
- Chorionic villi of human placenta
- Chorionic villi are mosaic
- Species differences: content of XIC (1)
- Comparing mouse and human XIC (1)
- Transfecting human XIST into the mouse
- Chimeric mice
- Human XIST inactivates the mouse X
- Mouse Tsix
- Function of mouse TSIX
- Finding the human TSIX
- Human TSIX is a truncated gene
- Comparing human and mouse TSIX (2)
- TSIX is co-expressed with XIST from inactive X
- TSIX is transcribed throughout gestation
- Summary of species differences in Tsix
- Evolution is a tinkerer (2)
- Random choice of active X
- The active X is chosen by repressing XIST
- Diploid cells have a single active X
- Triploid cells can have 2 active Xes
- Most triploids have cells with two active Xs
- The difference is in the autosomes
- Autosomal transfactor chooses active X
- Eliminating trisomy 11 as candidate autosome
- Using partial trisomes to find candidate genes
- Candidate regions on chromosomes 1 and 19
- Concluding remarks
Topics Covered
- Advantage of human model systems
- Silencing human inactive Xes
- Species differences in underlying mechanisms, specifically, in regard to parental imprinting and TSIX
- Choosing the single active human X and the role of autosomal transfactors in the process
Talk Citation
Migeon, B. (2016, June 29). X chromosome inactivation in human cells [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 26, 2024, from https://doi.org/10.69645/KFMN8010.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Barbara Migeon has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Biochemistry
Transcript
Please wait while the transcript is being prepared...
0:00
I am Barbara Migeon,
a member of the McKusick
Nathans Institute
of Genetic Medicine
at Johns Hopkins.
The title of my talk
is X Chromosome Inactivation
in Human Cell.
0:15
I will talk to you
about X chromosome inactivation,
the way mammals carry out
X dosage compensation.
This has been
the subject of previous talks
by Mary Lyon and Jenny Graves.
Although we hear a lot
about how the mouse
inactivates one X chromosome,
I will be talking
about the version
of X chromosome inactivation
in our own species.
First I will tell you
what we know
from studies of human cells
and human subjects.
Then I will talk about
how inactivating
human X chromosomes differ
from the process
in other species
and what might be responsible
for such differences.
And last, changing the focus
from inactive to active X,
I will tell you
why diploid human cells
have only a single active X,
no matter the number of Xs
in the cell
and how this active X is chosen.
1:17
Most studies of the early events
in X inactivation
have been carried out in mice
as it's been difficult to look
at human embryos at that time.
However, the study of humans
has other advantages.
Our phenotype is understood
better than that
of any other organism
and we can learn a good deal
from the study of cultured cell.
Also one X chromosome
can be isolated from the other
in hybrid cell.
Spontaneous abortions provide
a wealth
of X chromosome deletions
and different numbers
of X chromosome.
And now we have begun
to study human ES cells,
embryonic stem cells
and cleaving embryos left over
from in vitro fertilization.
We can also transfect
human genes into mice
for developmental study.
Furthermore, the fact
that humans are not inbred
and are in fact
very heterozygous
for many X-linked genes
has enabled studies
less feasible in other mammal.
Females are indeed
a genetic mosaic
as you see here,
with some cells expressing
the genes from their paternal X,
and others,
the genes from the maternal one.