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30 Terms

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Nucleotide

Building blocks of DNA, consisting of a five-carbon sugar, phosphate, and a nitrogenous base.

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Deoxyribose

The five-carbon sugar in DNA.

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Double helix

The shape formed by two strands of DNA that wrap around each other.

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Base pairing

The predictable matching of nitrogenous bases, where adenine pairs with thymine (A–T), and cytosine pairs with guanine (G–C).

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Genome

The complete set of DNA for a species.

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Chromosome

A distinct piece of DNA within a genome.

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Euchromatin

Loose form of DNA in the nucleus that is active and available for transcription.

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Heterochromatin

Condensed form of DNA in the nucleus that is generally inactive.

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DNA replication

The process of copying DNA from one molecule to two identical molecules.

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Helicase

The enzyme that unwinds the DNA double helix during replication.

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DNA polymerase

The enzyme that adds nucleotides to a growing DNA strand during replication.

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RNA primase

Enzyme that adds a short RNA primer to initiate DNA replication.

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Okazaki fragments

Short segments of DNA synthesized on the lagging strand during DNA replication.

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Semiconservative replication

Method of DNA replication where each new molecule contains one original strand and one new strand.

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Transcription

The process of making an RNA copy from DNA.

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mRNA

Messenger RNA, a type of RNA that carries the genetic code from DNA to the ribosome.

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Introns

Noncoding regions of mRNA that are removed during RNA processing.

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Exons

Coding regions of mRNA that are expressed and translated into proteins.

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Translation

The process of synthesizing proteins from mRNA.

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Codon

A sequence of three nucleotides in mRNA that codes for a specific amino acid.

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Ribosome

Cellular structure that assembles proteins by reading mRNA.

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Operon

A functioning unit of DNA in prokaryotes that contains a cluster of genes regulated by a single promoter.

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Mutation

An error in the genetic code that can result from DNA damage or incorrect repair.

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Point mutation

A mutation that involves a change in a single nucleotide base.

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Frameshift mutation

A mutation caused by insertions or deletions of nucleotides that alters the reading frame of codons.

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Conjugation

The transfer of genetic material between bacterial cells via direct contact.

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Recombinant DNA

DNA created by combining DNA from multiple sources.

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Polymerase Chain Reaction (PCR)

A laboratory technique used to amplify DNA, creating billions of identical copies.

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Gel electrophoresis

A technique that separates DNA fragments based on size and charge.

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Restriction fragment length polymorphisms (RFLPs)

Variations in DNA fragments that are caused by differences in genetic sequences.