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Flashcards covering DNA repair mechanisms, transcription, and translation processes in prokaryotes and eukaryotes.
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Hydrolysis
Loss of base from nucleotide, leading to an abasic (AP) site.
Alkylation
Addition of alkyl groups to bases or the phosphate backbone, leading to mispairing or strand breaks.
Deamination
Conversion of cytosine to uracil or adenine to hypoxanthine, causing transition mutations.
UV Light Damage
Causes pyrimidine dimers, which interfere with replication and transcription.
X-rays Damage
Induces single- and double-strand breaks and generates reactive oxygen species, leading to base damage.
Intercalating Agents
Molecules that insert between base pairs, causing insertions or deletions and resulting in frameshift mutations.
Base Analogs
Molecules that mimic natural bases, leading to mispairing and transition mutations.
Reactive Oxygen Species (ROS)
Cause oxidative base damage and lead to mutagenesis and strand breaks.
Chemical Adducts
Large molecules that covalently bind to DNA, distorting the helix and blocking replication.
Transition Mutations
Mutations that involve purine to purine or pyrimidine to pyrimidine substitutions.
Transversion Mutations
Mutations that involve purine to pyrimidine or vice versa substitutions.
Tautomeric Shifts
Temporary shifts in the proton position of bases that lead to mispairing during replication.
Direct Repair
Repair mechanism that reverses damage without replacing nucleotides, such as photoreactivation.
Excision Repair
Repair mechanism that excises damaged DNA and resynthesizes; includes BER and NER.
Translesion Synthesis (TLS)
Repair process that bypasses replication-blocking lesions with specialized low-fidelity DNA polymerases.
Mismatch Repair (MMR)
Corrects replication errors by recognizing mismatches and excising the erroneous DNA segment.
SOS Response
Bacterial response to severe DNA damage that induces multiple repair genes and leads to error-prone repair.
Base Excision Repair (BER)
Repair pathway that removes and replaces damaged bases in DNA.
Nucleotide Excision Repair (NER)
Repairs bulky lesions and helix-distorting damage in DNA.
UvrABC Nuclease
Nuclease involved in NER that detects and excises bulky lesions.
DNA Polymerase I
Fills in the gap during repair processes like NER and BER.
DNA Ligase
Seals nicks in the DNA strand after repair.
Photolyase
Enzyme that performs photoreactivation repair of UV-induced damage.
UvrD
Helicase that removes damaged DNA fragments during nucleotide excision repair.
MutS
Protein that recognizes mismatched bases during mismatch repair.
MutL
Protein that bridges MutS to MutH during mismatch repair.
MutH
Enzyme that cleaves the unmethylated strand at GATC sites during mismatch repair.
Negative Control Operons
Operons regulated by repressor proteins that inhibit transcription.
Positive Control Operons
Operons activated by activator proteins that enhance transcription.
Inducible Operon
Operon that is usually off and turned on in response to an inducer.
Repressible Operon
Operon that is usually on and turned off in the presence of a corepressor.
Silencers
Sequences that bind repressor proteins to inhibit transcription.
Enhancers
Sequences that bind activator proteins to enhance transcription.
Sigma Factor
Protein that aids RNA polymerase binding to the promoter in prokaryotes.
TATA Box
DNA sequence that functions as a promoter in eukaryotic transcription.
Rho-Independent Termination
Termination mechanism that relies on hairpin formation followed by a poly-U tail.
Rho-Dependent Termination
Termination mechanism involving the Rho protein catching up to RNA polymerase.
Eukaryotic RNA Polymerase I
Enzyme responsible for transcribing rRNA genes.
Eukaryotic RNA Polymerase II
Enzyme that transcribes mRNA and most non-coding RNAs.
Eukaryotic RNA Polymerase III
Enzyme that transcribes tRNA genes and 5S rRNA.
Nuclear RNA Processing
Includes capping, polyadenylation, and splicing of eukaryotic hnRNA.
Capping
Modification adding a 5' cap to mRNA to protect it from degradation.
Polyadenylation
Addition of a poly-A tail to the 3' end of mRNA to increase stability.
Spliceosome
Molecular complex responsible for splicing introns out of pre-mRNA.
mRNA Stability
Determined by the presence and length of the poly-A tail.
Heat-Shock Proteins
Proteins that assist in proper protein folding during stress.
Ubiquitination
Post-translational modification marking proteins for degradation by the proteasome.
Proteasome
Cellular complex responsible for degrading ubiquitinated proteins.
Chaperonins
Proteins that facilitate the proper folding of other proteins.
Ribosome Recycling Factor
Initiates the disassembly of the ribosome after translation termination.