Chapter 28. DNA Replication, Repair, and Recombination Flashcards

1
Q

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.

A

Mutagen

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2
Q

The dimeric β subunit of DNA polymerase III that forms a ring that surrounds the DNA duplex.

A

Sliding clamp

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3
Q

Enzymes that catalyze the ATP-driven unwinding of nucleic acids; DNA helicases are important in DNA replication.

A

Helicase

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4
Q

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.

A

DNA ligase

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5
Q

a means of repairing DNA in which a stretch of DNA around the site of damage is removed and replaced.

A

Nucleotide-excision repair

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6
Q

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.

A

Exonuclease

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7
Q

small fragments of DNA (approximately 1000 nucleotides) that are formed on the lagging strand at the replication fork of DNA synthesis and later joined.

A

Okazaki fragment

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8
Q

the newly synthesized strand of DNA at the replication fork that is synthesized continuously; see also lagging strand.

A

Leading strand

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9
Q

the newly synthesized strand of DNA at the replication fork that is initially synthesized as Okazaki fragments.

A

Lagging strand

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10
Q

a topological property of circular DNA, which is equal to the number of times a strand of DNA winds around the helix axis.

A

Linking number

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11
Q

the site of DNA synthesis where the parental strands are separated and daughter strands complimentary to each parent are synthesized.

A

Replication fork

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12
Q

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.

A

Processivity

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13
Q

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.

A

DNA polymerase

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14
Q

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.

A

Origin of replication

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15
Q

a specialized RNA polymerase that synthesizes the RNA primers for DNA synthesis.

A

Primase

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16
Q

a means of repairing damaged DNA in which the damaged region is corrected in place. For example, pyrimidine dimers are simply cleaved to restore the original nucleotides.

A

Direct repair

17
Q

DNA repair systems that consist of at least two proteins, one for detecting the mismatch and the other for recruiting an endonuclease that cleaves the newly synthesized DNA strand close to the lesion to facilitate repair.

A

Mismatch repair

18
Q

A means of repairing DNA in which the damaged base is removed and replaced by a base complementary to the undamaged DNA strand.

A

Base-excision repair

19
Q

in elongation of polymers, the initial segment of the polymer that is to be extended and on which elongation is dependent.

A

Primer

20
Q

A complex of DnaA, DnaB and DnaC proteins that bind at the origin of replication on the E. coli chromosome and make single-stranded DNA accessible to other proteins required for replication.

A

Origin of replication complex (ORC)

21
Q

a reverse transcriptase that contains its own template; a highly processive enzyme that elongates the 3 inch-ending strand of telomeres.

A

Telomerase

22
Q

A means for repairing double strand breaks in DNA that does not depend on other DNA molecules in the cell.

A

Nonhomologous end joining (NHEJ)

23
Q

The coordination of DNA replication and cell division in eukaryotes. Mitosis takes place only after DNA synthesis. Two gaps (G1 and G2) in time separate the two processes.

A

Cell cycle

24
Q

ends of chromosomes; the DNA at the telomere consists of hundreds of repeats of a hexanucleotide sequence characteristic of the organism.

A

Telomere

25
Q

a simple, rapid means of detecting carcinogens by measuring a chemical&#39s ability to induce mutations in Salmonella bacteria.

A

Ames test

26
Q

an enzyme that catalyzes the exchange of genetic material that occurs when two DNA molecules recombine.

A

Recombinase

27
Q

An E. coli protein central to recombination that can initiate recombination by promoting strand invasion.

A

RecA

28
Q

the initial stage in the recombination process in which four molecules of recombinase and their associated DNA molecules come together.

A

Recombination synapse

29
Q

a cross-like structure, formed by four polynucleotide chains, that is key intermediate in the recombination process.

A

Holliday junction

30
Q

Forming a structure of closed, circular DNA in which the DNA is more compact than the relaxed circular DNA; the circular DNA helix twists upon itself to form a superhelix.

A

supercoiling

31
Q

A model for DNA replication in which the lagging strand loops out of the replication complex with the loop lengthening and shortening, like the slide of a trombone, as replication proceeds.

A

Trombone model

32
Q

A measure of the helical winding of the DNA strands around each other in a double helix.

A

Twist

33
Q

a sequence of DNA or RNA which directs the production of a complementary sequence.

A

Template

34
Q

enzymes that catalyze the interconversion of topoisomers of DNA; topoisomerases can relax supercoiled DNA.

A

Topoisomerase

35
Q

A measure of the coiling of the axis of the double helix - that is, a measure of supercoiling.

A

Writhe

36
Q

molecules of DNA that differ from one another only in their linking number.

A

Topoisomer

37
Q

stretches of DNA in which a trinucleotide sequence is repeated many times. These segments of DNA can expand during DNA replication, causing genetic diseases, such as Huntington disease.

A

Trinucleotide repeat

38
Q

Genes for DNA-repair proteins that suppress tumor development when at least one copy of the gene is free of a deleterious mutation.

A

Tumor-suppressor gene