Chapter 28. DNA Replication, Repair, and Recombination Flashcards
perturbations to the base sequence of DNA that cause a mutation. Mutagens are often chemicals but can also be energy sources such as ultraviolet light.
Mutagen
The dimeric β subunit of DNA polymerase III that forms a ring that surrounds the DNA duplex.
Sliding clamp
Enzymes that catalyze the ATP-driven unwinding of nucleic acids; DNA helicases are important in DNA replication.
Helicase
an enzyme that catalyzes the formation of a phosphodiester bond between the 3 inch-OH at the end of one DNA chain and the 5 inch-phosphate at the end of the other chain; it is involved in the synthesis, repair, and splicing of DNA.
DNA ligase
a means of repairing DNA in which a stretch of DNA around the site of damage is removed and replaced.
Nucleotide-excision repair
an enzyme that digests nucleic acids from the ends of the molecule, rather than at an internal site. Exonucleases can be specific for digestion from the 3 inch or 5 inch ends of the nucleic acid.
Exonuclease
small fragments of DNA (approximately 1000 nucleotides) that are formed on the lagging strand at the replication fork of DNA synthesis and later joined.
Okazaki fragment
the newly synthesized strand of DNA at the replication fork that is synthesized continuously; see also lagging strand.
Leading strand
the newly synthesized strand of DNA at the replication fork that is initially synthesized as Okazaki fragments.
Lagging strand
a topological property of circular DNA, which is equal to the number of times a strand of DNA winds around the helix axis.
Linking number
the site of DNA synthesis where the parental strands are separated and daughter strands complimentary to each parent are synthesized.
Replication fork
a property of an enzyme that enables it to catalyze multiple rounds of elongation or digestion of a polymer while the polymer stays bound to the enzyme.
Processivity
enzymes that catalyze the template-directed, primer-dependent addition of deoxynucleotide units, using deoxynucleotide triphosphates as substrates, to the 3 inch end of the DNA chain; chain growth is in the 5 inch to 3 inch-direction; such enzymes replicate and repair DNA.
DNA polymerase
In general, the site on a chromosome where replication is initiated. The origin of replication site in E. coli has a length of 245 bp and contains a tandem array of three nearly identical 13-nucleotide sequences and five binding sites for the DnaA protein.
Origin of replication
a specialized RNA polymerase that synthesizes the RNA primers for DNA synthesis.
Primase