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DNA Repair
- Fix the damaged base
- photoreactivation - in bacteria, thymine dimers
formed by UV radiation are separated by DNA photolyase
using visible light as the energy source
- O6-methylguanine methyl transferase fixes guanines
that have been methylated by alkylating agents
- Excision repair - remove damaged bases and use a DNA
polymerase to replace them with the correct bases
- AP repair - DNA glycosylase removes damaged bases
from the sugar, the resulting apurinic or apyrimidinic
site (AP site) is removed from the DNA
- UV damage repair - excise area around thymine
dimer and resynthesize the strand
- Xeroderma pigmentosum - no UV repair, high skin
cancer rates and death by age 30
- Mismatch repair
- enzymes nick DNA on both sides of the mismatch,
Pol I and ligase do the rest
- how to recognize the "right" strand? In E. coli
the "old" DNA is methylated at G*ATC
- Recombination repair (post-replication repair)
- Pol III skips the damaged region, leaving a gap
- RecA promotes recombination with the sister duplex
(the damaged region is still there but the DNA is
intact)
- Error-prone repair (part of SOS response)
- RecA also has a protease activity that attacks a
regulatory protein called LexA
- w/o LexA the SOS genes are induced
- the SOS gene products allow DNA synthesis opposite
damaged DNA
- many mistakes are made, however, it's better than
nothing
Bell
CSU Chico
Library
This document is copyright of
Jeff
Bell
Last Update: Wednesday, August 12, 1998
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