DNA Structure, Replication, and Recombination

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Comprehensive vocabulary flashcards covering DNA structure, historical experiments (Griffith, Avery, Hershey-Chase, Watson-Crick), replication mechanisms, and recombination processes based on the lecture notes.

Last updated 2:39 AM on 6/4/26
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27 Terms

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Nuclein

Phosphorus-rich, weakly acidic material extracted from the nuclei of white blood cells by F. Meischer in 1869.

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Phosphodiester bonds

Covalent bonds that join adjacent nucleotides by connecting the 33' carbon of one nucleotide to the 55' carbon of the next.

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Transformation

The ability of a substance to change the genetic characteristics of an organism, as demonstrated by F. Griffith's 1928 experiments with Streptococcus pneumoniae.

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Transforming principle

The substance responsible for transforming nonvirulent R cells into virulent S cells; identified as DNA by Avery, MacLeod, and McCarty in 1944.

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Bacteriophages

Viruses that infect bacteria, consisting of roughly equal parts protein and DNA, used by Hershey and Chase to confirm DNA as the genetic material.

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Purine

A nitrogenous base with a two-ring structure (191-9 position numbering); examples include adenine (A) and guanine (G).

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Pyrimidine

A nitrogenous base with a one-ring structure (161-6 position numbering); examples include cytosine (C), thymine (T), and uracil (U).

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5' end and 3' end

The chemically distinct ends of a DNA polymer, designated by the presence of either a free 55' carbon or a free 33' carbon atom.

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Chargaff's rules

The observation that the ratio of A to T is 1:11:1 and the ratio of G to C is 1:11:1 in the DNA of most organisms.

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B-form DNA

The standard double helix structure which forms a right-handed helix and has a smooth backbone.

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Z-form DNA

A DNA variant that forms a left-handed helix and possesses an irregular backbone.

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Semiconservative replication

The Watson-Crick model of replication where the two strands of the parental double helix separate, each serving as a template for a new complementary strand.

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Conservative replication

A hypothetical model where the parental double helix remains intact and the daughter helix is composed of two entirely new strands.

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Dispersive replication

A hypothetical model where both strands of the daughter helices contain a mixture of parental and newly synthesized DNA.

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DNA polymerase III

The enzyme in E. coli that catalyzes the formation of new phosphodiester bonds during the elongation stage of DNA replication.

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Initiation

The first stage of DNA replication where proteins open the double helix at the origin of replication and prepare it for base pairing.

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DNA Helicase

An enzyme that unwinds the DNA double helix during the initiation of replication.

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Single-strand binding proteins (SSBs)

Proteins that bind to the unwound DNA strands to keep the helix open during replication.

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Primase

An enzyme that synthesizes short RNA primers that are complementary and antiparallel to the DNA template strands.

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Leading strand

The DNA strand that undergoes continuous synthesis in the 55' to 33' direction toward the replication fork.

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Lagging strand

The DNA strand that undergoes discontinuous synthesis in the form of short segments called Okazaki fragments.

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Okazaki fragment

Short DNA fragments synthesized on the lagging strand during DNA replication.

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DNA polymerase I

The enzyme that replaces RNA primers with DNA sequences during the elongation process.

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DNA ligase

The enzyme that covalently joins successive Okazaki fragments together and seals nicks in the sugar-phosphate backbone.

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DNA topoisomerase

An enzyme that relaxes supercoils created by unwinding DNA by cutting and re-sealing the sugar-phosphate backbone.

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Gene conversion

The physical change of one allele in a heterozygote to the other, often occurring via mismatch repair in a heteroduplex region.

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DNA Polymerase II

An enzyme involved in DNA repair and the synthesis of new DNA strands during DNA replication, particularly in the replication of damaged DNA in prokaryotes. It plays a secondary role in DNA replication compared to DNA polymerase III.