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Printable Handouts
Navigable Slide Index
- Introduction
- Lecture outline
- Introduction to chromatin structure
- Primary function of chromatin: DNA compaction
- Multiples levels of DNA packaging
- The nucleosome core particle
- The histone octamer is a tripartite structure
- Chromatin rearrangements during S-phase
- De novo nucleosome assembly during cell cycle
- DNA replication slows down during S-phase
- Coupling of DNA replication and histone synthesis
- DNA replication without nucleosome assembly
- Chromatin structure restoration during replication
- Chromatin structure restoration: H3-H4 tetramers
- Nucleosome assembly onto nascent DNA
- DNA replication-coupled nucleosome assembly
- Problem of histone-DNA aggregation
- The de novo nucleosome assembly line
- Chromatin assembly factor 1 (CAF-1) and PCNA
- PCNA and PCNA-binding proteins
- ASF1: a multi-talented histone chaperone
- Acetylation of newly synthesised H3 and H4
- B-type HATs
- Acetylation of new histones is transient
- Biomedical implications
- Implication of acetylation/deacetylation blockage
- HDAC inhibitors in clinical trials
- Epigenetic inheritance
- Acetylation / deacetylation / epigenetic inheritance
- Duplication of histone epigenetic marks
- Potential targets for cancer therapy
- Potential targets for regenerative medicine
- Summary of biomedical implications
Topics Covered
- Introduction to chromatin structure
- Primary function of chromatin: DNA compaction
- The nucleosome core particle
- De novo nucleosome assembly during the cell cycle
- Two distinct processes contribute to restoration of chromatin structure during DNA replication
- A fundamental problem in nucleosome assembly: histone-DNA aggregation
- Chromatin Assembly Factor 1 (CAF-1) and PCNA
- ASF1: a multi-talented histone chaperone
- Biomedical implications
- Agents that block the acetylation and deacetylation of new histones may sensitise cells to cancer chemotherapeutic agents
- Genome-wide histone acetylation, deacetylation and epigenetic inheritance
- Epigenetic xerox machines as potential targets for cancer therapy and regenerative medicine
Talk Citation
Verreault, A. (2019, December 4). Nucleosome assembly during DNA replication [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 26, 2024, from https://doi.org/10.69645/NHET7731.Export Citation (RIS)
Publication History
Financial Disclosures
- Dr. Alain Verreault has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Genetics & Epigenetics
Transcript
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0:00
My name is Alain Verreault, and
I'm an associate professor in
the Department of Pathology and
Cell Biology at
the University of Montreal.
And my group studies
nucleosome assembly during DNA
replication at the Institute for
Research in Immunology and Cancer.
0:24
The aim of this lecture is
to describe the process of
nucleosome assembly coupled
to DNA replication.
I also intend to explain some
of the physiological and
biomedical implications of this
important but poorly understood pathway.
Whenever appropriate,
references to original papers or
reviews are indicated at
the bottom of each slide.
I've divided this lecture
into four sections.
First, I'll describe the generic
structure of chromatin.
In the second part,
I will present an overview of chromatin
rearrangements that occur during
S-phase of the cell cycle.
The third portion of my presentation
will focus on the replication-coupled
nucleosome assembly.
And the final segment of the lecture
will describe some of the biomedical
implications of replication-coupled
nucleosome assembly.
1:26
The primary function of histones
in chromatin is to package DNA
within the cell nucleus.
The sheer magnitude of DNA compaction
that is necessary to package
human DNA can be illustrated
with a few telling numbers.
Each cell in the human body contains a
total length of about 2 meters of DNA that
is confined within a cell nucleus whose
diameter is only about 10 micrometers.
A simple calculation reveals
that the total length of DNA
in an average-sized human body
is equivalent to a staggering
1,500 round trips from
the Earth to the sun.
The obvious challenge is to
package this enormous amount of
DNA in a form that allows regulated access
to genetic information whenever necessary.