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Printable Handouts
Navigable Slide Index
- Introduction
- Outline
- DNA damage and repair systems
- Basic structure of DNA
- Dimensions of DNA
- Gene organization
- Gene organization: repeated DNA sequences
- The central dogma
- The genetic code
- Amino acids and protein folding
- What can go wrong? Single base-pair mutations
- What can go wrong? Frameshift mutations
- What can go wrong: significant mutations
- Genome stability
- DNA structure: Watson and Crick model
- Eukaryotic DNA replication
- Ensuring accuracy in DNA replication
- 5’ to 3’ exonuclease activity of DNA polymerases δ and ε: proofreading
- DNA polymerase proofreading is driven by conformational changes
- Mismatch repair
- Mismatch repair in E. coli (1)
- Mismatch repair in E. coli (2)
- Mammalian mismatch repair
- Inherited and acquired de novo mutations
- Oxidative DNA damage and Base Excision Repair (BER)
- UV-induced photodimer
- Reversing UV-induced photodimers
- Translesion synthesis
- Primase Polymerase (PrimPol)
- Template switching at a stalled replication fork
- Nucleotide Excision Repair (NER) of UV-induced photodimers
- NER of UV-induced photodimers in mammalian cells
- Transcription-coupled repair (2024)
- Inter-strand crosslink repair
- Inter-strand crosslinking agents
- Alcohol flush reaction
- Structural variants (irreparable mutations)
- Putting broken ends back together
- Nonhomologous end-joining
- Microhomology-mediated end-joining
- Intragenic deletions
- Single-strand annealing between repeats flanking a double-strand break
- Rad51-mediated homologous recombination repair of replication breaks
- Financial disclosures
Topics Covered
- DNA structure, genes, genetic codes and mutations
- Mutational errors of DNA replication and DNA polymerase proof reading
- Mismatch repair
- Oxidative and UV-induced DNA damages
- Nucleotide excision repair
- Base excision repair -Translesion synthesis
- Mechanisms for double strand break repair
Links
Categories:
External Links
Talk Citation
Haber, J. (2026, February 26). Preserving the genome: repair of DNA damage [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved April 18, 2026, from https://doi.org/10.69645/NPPH9044.Export Citation (RIS)
Publication History
- Published on February 26, 2026
Financial Disclosures
- Prof. James Haber has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Genetics & Epigenetics
Transcript
Please wait while the transcript is being prepared...
0:00
Hello. My name is Jim Haber.
I'm a professor of biology at
Brandeis University in Waltham,
Massachusetts,
outside of Boston.
I study how DNA is repaired.
I have been doing
so for a long time.
In fact, when I went
to college in 1961,
it was the same year
that messenger RNA
was hypothesized and
then demonstrated,
the same year that
the lactose repressor
was postulated, and
the same year that
the triplet genetic
code was deciphered.
So, I've had an
opportunity to follow
this field for a long time.
0:36
I'm going to talk about how
our DNA is repaired
and preserved.
To begin with, I will say
something about the
structure of DNA and
remind you about the
structure of genes
and the organization
of the genetic code,
and then talk about a number of
different ways in which
damage occurs to DNA,
and which our cells have
the capacity to repair.
1:00
There are, in fact, many
different assaults on DNA,
changes that happen during
the copying of DNA,
changes that happen because
our DNA is exposed
to oxidative damage,
damage that occurs by accidental
breaks in the DNA sequence,
and even more serious
breaks that rupture
both strands of DNA
so that the DNA is
no longer connected,
for example, to its centromere.
I'll talk a little bit about
each of these, although most of
the discussion of
double-strand break repair
will actually be in
another lecture.
1:39
Just to remind you,
DNA is a double helix, as
you undoubtedly remember.
It is made up of base pairs
between two purines
and two pyrimidines:
cytosine, thymine,
adenine, and guanine.
These bases are arranged
such that As pair with Ts,
Gs pair with Cs, and that
this pairing between
these bases then leads to the
structure of a double helix,
in which the two strands are
in an antiparallel arrangement
and the pairing between
these bases assures
that they can be
properly replicated.