DNA - The Code of Life and RNA Flashcards

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A comprehensive set of vocabulary flashcards covering the structure of DNA and RNA, protein synthesis, mutations, and DNA technology based on the lecture notes.

Last updated 3:33 PM on 8/19/26
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32 Terms

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Nucleoplasm

A jelly-like liquid enclosed by the nuclear membrane within the nucleus.

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Chromatin network

A mass of thread-like structures in the nucleus that coils and thickens into chromosomes during cell division.

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Chromosomes

Long, thin, thread-like structures composed of DNA wrapped around proteins called histones; they are the carriers of genetic material.

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Extranuclear DNA

DNA that occurs outside the nucleus, specifically in the mitochondria of plants and animals and the chloroplasts of plant cells.

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Mitochondrial DNA (mtDNA)

DNA found in the mitochondria that is inherited only via the maternal line and used to trace maternal ancestry due to its relative lack of mutation.

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Gene

A short segment of a DNA molecule that codes for a particular protein and controls an inherited characteristic.

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Nucleic acids

Organic molecules, specifically DNA and RNA, that control protein synthesis by storing and transferring genetic information.

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James Watson and Francis Crick

Scientists who formulated the double helix structure of DNA in 1953 using a three-dimensional model.

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Rosalind Franklin

A scientist who took X-ray photographs of DNA in 1952 and surmised its helix shape, though she died before the Nobel Prize was awarded.

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Friedrich Miescher

The scientist who identified DNA in 1874.

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Erwin Chargaff

A scientist who determined in 1949 that there are equal numbers of Adenine and Thymine bases (A=TA = T) and equal numbers of Guanine and Cytosine bases (G=CG = C) in a DNA molecule.

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Nucleotides

The monomers or building blocks of DNA or RNA, each consisting of a sugar molecule, a phosphate group, and a nitrogenous base.

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Purine bases

Large nitrogenous bases known as Adenine (A) and Guanine (G).

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Pyrimidine bases

Smaller nitrogenous bases known as Cytosine (C) and Thymine (T) in DNA, or Uracil (U) in RNA.

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Hydrogen bonds

Weak bonds that join nitrogenous bases; two bonds form between Guanine and Cytosine, and three form between Guanine and Cytosine.

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Non-coding DNA

Approximately 98%98\% of DNA that does not carry information to produce proteins; it is used in DNA fingerprinting and regulates gene expression.

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DNA replication

The process taking place during Interphase where a DNA molecule duplicates to form two identical copies (replicas).

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Chromatids

Two identical units formed when a chromosome duplicates during replication, held together by a centromere.

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DNA polymerase

The specific enzyme responsible for joining free-floating nucleotides to build a complementary DNA strand during replication.

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Messenger RNA (mRNA)

A single-stranded RNA formed in the nucleoplasm using DNA as a template; it carries the genetic code from the nucleus to the ribosomes.

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Transfer RNA (tRNA)

A single-stranded RNA that folds into loops, contains an anticodon, and picks up specific amino acids in the cytoplasm to bring them to the ribosomes.

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Transcription

The process where mRNA obtains the genetic code for protein synthesis from a DNA template in the nucleus.

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Translation

The process where the code in the mRNA strand is used to form a specific sequence of amino acids to synthesize a protein at the ribosome.

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Codon

A group of three nitrogenous bases on the mRNA molecule that codes for a particular amino acid.

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Anticodon

A sequence of three exposed nitrogenous bases on a tRNA molecule that is complementary to an mRNA codon.

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Base triplet

Three consecutive nitrogenous bases on a DNA strand that provide the code for a particular amino acid.

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Mutation

Any change in the genetic composition of an organism, which can occur spontaneously or via mutagens.

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Mutagens

Physical or chemical agents, such as X-rays, UV light, or toxic chemicals, that cause mutations.

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Substitution mutation

A point mutation where one nitrogenous base is replaced by another, altering only one amino acid.

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Frameshift mutation

A mutation caused by the deletion or insertion of nitrogenous bases (not in multiples of three), which alters all subsequent base triplets.

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DNA profiling (DNA fingerprinting)

A process where a 'barcode' pattern is obtained from non-coding DNA to identify individuals or determine paternity.

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Polymerase Chain Reaction (PCR)

A technology used to replicate and multiply small samples of DNA into millions of segments for testing in DNA fingerprinting.