Terminology
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5,10-Methenyltetrahydrofolate - A molecule that acts like 8-hydroxy-5-deazaflavin
in DNA photolyases. It acts as a light harvesting factor.
5-Methylcytosine - The only methylated base found in eukaryotic
DNA
6-4 Photoproduct - A structure in DNA of a covalent link
made between carbon #4 of the 3' pyrimidine and carbon #6 of an
adjacent 5' pyrimidine. It occurs as a result of exposure to UV
light. It can lead to mutation during replication. Figure
25.9.
8-Hydroxy-5-deazaflavin - A molecule that acts like 5,10-methenyltetrahydrofolate
in DNA photolyases. It acts as a light harvesting factor.
8-Oxoguanine - An oxidized form of guanine arising from
oxidative damage.
attB - A locus in the E. coli chromosome
targeted by the bacteriophage
for site-specific
recombination. Figure 25.31.
attP The site on the
chromosome
involved in site-specific recombination with the E. coli
chromosome. Figure 25.31.
Base Excision Repair - Cellular DNA repair system that cleaves
the glycosidic bond connecting a damaged base to the DNA sugar-phosphate
backbone.
BRCA-1 - A gene associated with an increased risk of breast
and ovarian cancer that is involved in transcription-coupled excision
repair.
Chi - An octanucleotide sequence in E. coli (5'-GCTGGTCC-3')
recognized by exonuclease V. At this sequence, the exonuclease
switches strands and its preferred polarity of DNA degradation.
This facilitates the loading of RecA to a free 3' end and initiates
strand invasion of a nearby duplex. Figure
25.28
Chromophore - A
structural moiety that absorbs light of characteristic wavelengths.
Figure 25.10
Clonal Expansion
- A mechanism by which large-scale production of specific antibodies
occurs. The B and T cells produced by the body have randomly generated
antigen specificities. When a particular antigen enters the body,
it induces proliferation only in B and T cells that happen to
be specific for it. Thus, the antigen selects the cells that will
mount an immune response against it and stimulates them to undergo
clonal proliferation.
Cyclobutane Pyrimidine Dimer - A structure in DNA of two
covalent bonds made between adjacent pyrimidine residues as a
result of exposure to UV light. The two new bonds form a four-membered
ring and can lead to mutation during replication if not repaired.
Figure 25.9
DNA Photolyase -
An enzyme that repairs cyclobutane pyrimidine dimers in the presence
of visible light. Figure 25.10.
Excinuclease - A term used to describe the enzymatic cutting
of DNA by the uvrABC system.
Exonuclease V (also called RecBCD nuclease) - A protein
in E. coli recombination that binds at a double-strand
break on duplex DNA and uses a helicase activity to unwind and
partially degrade the DNA. It helps to load RecA to a 3' end.
Figure 25.28
Gene Amplification
- Selective amplification of a specific region of a genome
Heteroduplex - A double stranded DNA in which the two strands
were not made from each other and came from other molecules. Figure 25.19
Holliday Junction
- An intermediate during homologous recombination; a four-armed
structure in which each of the participating DNA duplexes has
exchanged one strand with the other duplex. Figure
25.20
Holliday Model -
A model for homologous recombination involving alignment of homologous
sequences, nicking, strand invasion, ligation, migration of the
cross point (Holliday Junction), isomerization, breaking of strands,
and rejoining. A variation of the model was proposed by Meselson
and Radding. Figure 25.20
Homogeneously Staining
Region - A region of a chromosome that lacks the typical
chromosome banding pattern. It can be produced by gene amplification.
Homologous Recombination - Genetic recombination that requires
extensive sequence homology between the recombining DNA molecules.
Meiotic recombination by crossing over in eukaryotes is an example.
Illegitimate Recombination - An extremely rare type of
recombination that possibly occurs by chance. It involves neither
sequence homology nor the action of any known protein.
Immunoglobulin G (IgG) - An antibody of class 'G' containing
two heavy chains and two light chains.
Maintenance Methylase - A eukaryotic enzyme that ensures
that all of the methylated sites in the parental DNA are also
methylated in the progeny DNA. Figure
25.3
Meselson -Radding Model
- A proposed model for homologous recombination involving alignment
of homologous sequences, nicking, strand displacement synthesis,
strand invasion, loop cleavage, ligation of the displaced strand,
isomerization, branch migration and ligation of the invading 'A'
strand, and resolution as in the Holliday model. Figure
25.22
Microsatellite Instability - Mutations consisting of repeats of single, double,
and triple-nucleotide sequences which probably arise by 'slipping'
of strands during DNA polymerization.
Mismatch Repair - Cellular DNA repair system that recognizes
DNA mismatches created either by replication errors, non-homologous
recombination, or damage to one DNA base, and corrects the error.
Mutagenesis - The process of creating mutations.
mutT - An E. coli gene that catalyzes the
following reaction: 8-oxo-dGTP + H2O <=> 8-oxo-dGMP + PPi
Nucleotide Excision Repair - A process whereby a damaged
section of a DNA chain is cut out, or excised, followed by the
action of DNA polymerase and then DNA ligase to regenerate a covalently
closed duplex at the site of the original damage.
O6-Alkylguanine Alkyltransferase - An unusual repair enzyme that transfers a methyl
or ethyl group from an O6-methylguanine or O6-ethylguanine to a cysteine residue in the active site
of the protein. It can thus, only function once.
Oncogenic Transformation - Conversion of a normal cell
to a cancerous one.
Photoproducts - The products that result when light energy
causes a chemical reaction to occur in a substance. With respect
to DNA, the term refers to the types of damaged DNA that can be
caused by uv irradiation.
Plaque - A cleared area on a Petri dish on a plate of bacteria
arising from growth of a bacteriophage in that region.
Postreplication Repair - Processes that attempt to fix
mismatches, gaps, or damage to DNA that escapes the repair process
that occurs during replication
Prophage - The integrated, inactive
chromosome
in the E. coli genome.
Provirus - With respect to a retrovirus, a virus integrated
into the host genome.
RecA - A multifunctional protein with Mr of about 38,000.
In recombination it promotes the pairing of homologous strands.
In the SOS response it also plays a role in gene activation. Figure 25.23
Recombination -
A process in an organism in which two parent DNA molecules give
rise to daughter DNA that combines segments from both parent molecules.
It may involve the integration of one DNA molecule into another,
the substitution of a DNA segment for a homologous segment on
another DNA molecule, or the exchange of homologous segments between
two DNA molecules.
Recombinational Repair - Cellular DNA repair system in
which newly replicated DNA duplexes undergo genetic recombination,
with ultimate removal of the damaged DNA segment.
Resolvase - An enzyme found in class II and class III type
transposons that catalyzes site-specific recombination between
the two elements of the transposon created by replicative transposition.
Restriction Endonucleases - Enzymes that catalyze the double-strand
cleavage of DNA at specific base sequences.
Restriction/Modification - A defense system common in bacteria
involving a restriction endonuclease and a site-specific methylase
that methylates the same sequence the restriction endonuclease
cuts at. Normally, the host DNA is methylated, which protects
against the action of the restriction endonuclease, but invading
viral DNA is not methylated, and is cut. Figure
25.5
Retrotransposon
- A transposable element which goes through an RNA stage.
Retroviruses - A family of RNA viruses that possess reverse
transcriptase. After the virus infects a cell, this enzyme transcribes
the RNA genome into a double-strand DNA version, which integrates
into a host chromosome. Human immunodeficiency virus (HIV) is
an example.
ruvA - A protein involved in E. coli recombination.
It is a DNA binding protein, whose specificity directs it toward
the four-stranded Holliday structure
ruvB A protein involved in E. coli recombination.
It is an ATP-requiring motor protein, which binds to two opposed
arms of the Holliday junction and rotates them in opposite directions,
forcing branch migration by driving the rotational movement of
the other two strands toward the junction.
ruvC A protein involved in E. coli recombination.
It begins resolution of the Holliday structure by nicking two
strands.
Site-specific Recombination - Recombination that involves
only limited sequence homology between recombining partners. Sites
of breaking and joining are determined by specific DNA-protein
interactions. Figure 25.17
Somatic Mutations
- Mutations that occur in non-germline cells.
SOS Response - A bacterial response to various potentially
lethal stresses, including severe UV irradiation. It involves
the coordinated expression of a set of proteins that carry out
survival maneuvers, including an error-prone type of repair for
thymine dimers in DNA.
Strand Invasion - A process that is postulated to occur
in homolous recombination in which an unpaired part of a strand
of DNA invades a duplex region of another DNA.
Thymine Glycol - An oxidized form of thymine arising from
oxidative damage.
Transition Mutation - A mutation that changes a purine-pyrimidine
base pair to a different purine-pyrimidine base pair. An example
is a transition from G-C to A-T.
Transposable Genetic Elements - DNA fragments containing
genes that do not have a fixed location in a genome but can move
from place to place within the genome, albeit with low frequency.
Figure 25.34.
Transposase - An enzyme involved in movement of a transposon
from one DNA to another. It can make a staggered cut in a specific
sequence in a target DNA into which the transposon moves.
Transposition - A type of recombination which involves neither sequence
homology nor the RecA protein (in E. coli) but does require
a special sequence on the donor DNA.
Tranverse Mutation - A mutation that changes a purine-pyrimidine
base pair to a different pyrimidine-purine base pair. An example
is a transition from G-C to T-A.
Unequal Crossing Over - A recombinational process that
can lead to multiple copies of a gene. It may be important in
gene amplification.
uvrD - A helicase component of the E. coli
nucleotide excision repair system.
Xis - A protein required in addition to Int and IHF to
reverse the process by which
was integrated
into the E. coli genome.