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A comprehensive set of 80 vocabulary flashcards covering DNA replication models, enzymes, repair mechanisms, and associated diseases as detailed in the lecture transcript.
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Semiconservative model
DNA replication model where each daughter DNA double helix contains one parental strand and one newly synthesized strand.
Conservative model
A model of DNA replication that was ruled out by the Meselson–Stahl experiment.
Dispersive model
DNA replication model ruled out after the second round of replication in the Meselson-Stahl experiment.
Meselson–Stahl experiment
Study that labeled bacteria with heavy and light nitrogen isotopes to determine the mode of DNA replication.
15N
The heavy isotope of nitrogen used to label DNA in the Meselson–Stahl experiment.
14N
The light isotope of nitrogen used to label DNA in the Meselson–Stahl experiment.
Replication origins
Specific sites on eukaryotic chromosomes where DNA synthesis begins; eukaryotic chromosomes have multiple of these.
Replication forks
Y-shaped junctions that form at each replication origin and move away from each other as replication proceeds.
DNA polymerase
Enzyme that catalyzes the addition of nucleotides to the 3′ end of a growing DNA strand using a parental template.
DNA polymerase β
Eukaryotic polymerase primarily involved in the repair of DNA damage.
DNA polymerase γ
Polymerase responsible for the replication of mitochondrial DNA.
DNA polymerase α
One of the polymerases involved in chromosomal DNA replication and copying the ends of linear chromosomes.
DNA polymerase δ
Polymerase involved in chromosomal DNA replication and filling gaps in the lagging strand during repair.
DNA polymerase ε
One of the major polymerases involved in eukaryotic chromosomal DNA replication.
Arthur Kornberg and Sylvy Ruth Levy
Researchers mentioned in the transcript associated with DNA polymerase.
5′-to-3′ direction
The fundamental direction in which all known DNA polymerases synthesize DNA.
Deoxyribonucleoside triphosphates
The chemical form in which nucleotides enter the DNA synthesis reaction.
Pyrophosphate (PPi)
A chemical group released when a nucleoside triphosphate is covalently linked to a growing DNA strand.
Asymmetrical replication fork
A structure where one new DNA strand is made continuously and the other is made in short pieces.
Leading strand
The new DNA strand that is synthesized continuously in the 5′-to-3′ direction.
Lagging strand
The DNA strand synthesized as a series of short fragments (Okazaki fragments) in the 5′-to-3′ direction.
Okazaki fragments
Short DNA pieces synthesized on the lagging strand that are later joined together.
DNA helicase
Enzyme that uses the energy of ATP hydrolysis to unwind the DNA double helix ahead of the replication fork.
Single-strand DNA-binding protein
Protein that binds to exposed DNA to prevent base pairs from re-forming before replication.
Sliding clamp
Protein that keeps DNA polymerase attached to the template during synthesis.
Clamp loader
Protein that uses ATP hydrolysis to lock the sliding clamp onto the DNA.
Primase
Enzyme that synthesizes short lengths of RNA to act as primers for DNA synthesis.
RNA primers
Short lengths of RNA, about 200 nucleotides apart in eukaryotes, that initiate DNA synthesis.
Nuclease
Enzymes that remove RNA primers during the synthesis of the lagging DNA strand.
DNA ligase
Enzyme that joins Okazaki fragments by using ATP to activate the 5′ phosphate of one fragment.
Taq DNA polymerase
First heat-resistant enzyme sourced from Thermus aquaticus used for PCR.
Thermus aquaticus
Species of bacteria that can tolerate high temperatures and provides the enzyme for PCR.
PCR (Polymerase Chain Reaction)
Process that can produce over a million-fold copy of target DNA within a few hours.
Torsional stress
Tension developed during replication and transcription, relieved by supercoiling or topoisomerases.
DNA topoisomerases
Enzymes that relieve torsional stress by generating temporary nicks in the DNA backbone.
Topoisomerase I
Enzyme in all cells that cleaves one strand of DNA to allow unwinding, producing a relaxed-circle conformation.
Type II topoisomerase
Eukaryotic homodimers that use a two-gate mechanism to manage DNA transport and relieve tension.
N-gate
The component of type II topoisomerase that traps a second DNA segment upon ATP binding.
T-segment
The second DNA segment that is captured and pushed through the DNA-gate in type II topoisomerase.
DNA-gate
The gate in topoisomerase II that opens to allow the T-segment to pass through the G-segment.
C-gate
The C-terminal gate that opens to release the T-segment from the type II topoisomerase.
Gyrase
The bacterial (E.coli) Type IIA topoisomerase.
Decatenase
The bacterial (E.coli) Type IV topoisomerase used for unlinking daughter chromosomes.
Nuclear localization sequences (NLS)
Sequences contained in the C-terminal domain of Human Type IIα topoisomerase.
Telomerase
Enzyme that replicates the ends of eukaryotic chromosomes by extending the template strand.
1 incorrect base per 109 to 1010 nucleotides
The approximate error rate of DNA replication after correction.
Proofreading
The self-correcting property of DNA polymerase that removes incorrectly paired nucleotides.
P mode
The polymerizing mode of DNA polymerase.
E mode
The editing or proofreading mode of DNA polymerase that cleaves incorrect nucleotides.
Depurination
Chemical reaction that removes guanine or adenine from DNA, occurring 5000 times per cell per day.
Deamination
Reaction that converts cytosine to uracil, occurring to about 100 bases per cell per day.
Thymine dimers
Damage where two adjacent thymine bases become covalently attached due to ultraviolet radiation.
Base excision repair (BER)
Mechanism that involves the removal of a mismatched T and replacement with a C.
Apurinic endonuclease I (APE1)
Enzyme that cuts the DNA backbone at the abasic site during base excision repair.
Nucleotide excision repair (NER)
System that recognizes double-helix distortions and repairs thymine dimers.
XP (xeroderma pigmentosum) protein complex
A protein group that repairs UV-induced DNA damage; mutations cause skin cancer predisposition.
Mismatch excision repair
Repair system using the MSH2-MSH6 complex to remove errors that escape proofreading.
Lynch Syndrome
Hereditray predisposition to nonpolyposis colorectal cancer caused by MSH2 or MLH1 mutations.
Methyl mismatch repair (MMR)
Bacterial system using MutS, MutL, and MutH to fix mismatches based on DNA methylation.
MutS
Bacterial protein that recognizes the DNA mismatch in the MMR system.
Nonhomologous end joining
Double-strand break repair strategy where ends are cleaned and joined, often losing nucleotides.
Homologous recombination
Flawless repair strategy for double-strand breaks using an undamaged double helix as a template.
H2AX
Histone protein whose phosphorylation on serine 139 helps direct DNA damage repair pathways.
Sickle-cell anemia
Disease caused by a single nucleotide change changing glutamic acid to valine in β-globin.
Colon cancer
A disease caused by the accumulation of multiple mutations, with incidence increasing with age.
arCpG
Age-related CpG sites that show increased or decreased methylation status with age.
Age-related methylation
Epigenetic changes that can cause the silencing of tumor suppressor genes.
1000 nucleotides per second
The rate of DNA replication in bacteria.
100 nucleotides per second
The rate of DNA replication in eukaryotes.
DNA pol I
Bacterial enzyme responsible for the removal of RNA primers.
RNase H
Eukaryotic enzyme responsible for the removal of RNA primers.
DNA pol III
Bacterial enzyme responsible for strand elongation.
Replication bubble
Structure formed by two replication forks moving in opposite directions away from an origin.
G-segment
The DNA segment bound and bent by type II topoisomerase that is eventually cleaved.
Melanoma
A type of skin cancer that hereditary xeroderma pigmentosum predisposes individuals toward.
MutH
Bacterial enzyme in the MMR system that cleaves the unmethylated GATC sequence.
ATPase
Function of Human Type IIα topoisomerase that hydrolyzes ATP.
Tyrosyl residue
Active site component of topoisomerases that binds with DNA.
Type IIB
Classification of type II topoisomerases found in Archaea.
Flush ends
Level ends produced when nucleases "chew back" broken double-strand DNA during nonhomologous end joining.