DNA, RNA, and Protein Synthesis
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Questions and Answers

Who discovered transformation while studying pneumonia in mice?

  • Avery
  • Hershey and Chase
  • Griffith (correct)
  • Watson and Crick

Avery built on Griffith's experiment to prove that DNA, not proteins, was the genetic material.

True (A)

Hershey and Chase used a radioactive isotope of sulfur to label proteins.

True (A)

What type of virus infects bacteria?

<p>Bacteriophage</p> Signup and view all the answers

What is Chargaff's rule?

<p>A = T and C = G</p> Signup and view all the answers

Flashcards

Griffith

Discovered transformation while studying pneumonia in mice.

Avery

Discovered that DNA was responsible for transferring genetic information. Built off Griffith's experiment.

Hershey and Chase

Used radioactive material to label DNA and protein; helped prove that DNA is genetic material, not proteins

Sulfur-35

radioactive forms of sulfur used in protein labeling

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Phosphorus-32

radioactive forms of phosphate used in DNA labeling

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Bacteriophage

A virus that infects bacteria

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Chargaff's Rule

A=T and C=G

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Nucleotide

A building block of DNA, consisting of a five-carbon sugar covalently bonded to a nitrogenous base and a phosphate group.

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Nitrogen bases

The chemicals that make up the rungs of the DNA ladder. A-T and C-G match.

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Hydrogen bonds in DNA

Weak bonds that hold base pairs together

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Phosphate in DNA

Makes up the backbone of DNA; connected to deoxyribose sugar.

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Deoxyribose

A five-carbon sugar that is a component of DNA nucleotides

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Rosalind Franklin

Generated x-ray images of DNA; her image was provided to Watson and Crick with key data about DNA

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Watson and Crick

Developed the double helix model of DNA.

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Histones

protein molecules around which DNA is tightly coiled in chromatin

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Nucleosome

Bead-like structure in eukaryotic chromatin, composed of a short length of DNA wrapped around a core of histone proteins

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Helicase

An enzyme that unzips DNA by breaking the hydrogen bonds at the replication forks.

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Replication fork

a Y-shaped point that results when the two strands of a DNA double helix separate so that the DNA molecule can be replicated

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DNA polymerase

Enzyme involved in DNA replication that joins individual nucleotides to produce a DNA molecule. Also edits the DNA.

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RNA

single-stranded nucleic acid that contains the sugar ribose and has uracil instead of thymine

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mRNA

messenger RNA; type of RNA that carries instructions from DNA in the nucleus to the ribosome

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tRNA

transfer RNA; type of RNA that carries amino acids to the ribosome

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rRNA

ribosomal RNA; type of RNA that makes up part of the ribosome

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Telomere

repeating DNA bases at the ends of chromosomes that do not form genes and help prevent the loss of genes

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Telomerase

An enzyme that catalyzes the lengthening of telomeres.

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Transcription

synthesis of an RNA molecule from a DNA template

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Translation

Process by which mRNA is decoded and a protein is produced

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Codon

Three consecutive bases that code for a specific amino acid.

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Promoter

specific site where RNA polymerase can bind and begin transcription

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Introns

sequence of DNA that is not involved in coding for a protein; junk DNA

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Exons

Coding segments of eukaryotic DNA; code for proteins.

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Point mutation

gene mutation in which a single base pair in DNA has been changed

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Duplication mutation

A genetic mutation in which a region that contains a gene or an entire chromosome is duplicated, which results in multiple copies of that region or nucleotide.

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Substitution

A mutation in which a nucleotide or a codon in DNA is replaced with a different nucleotide

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Deletion mutation

a mutation in which one or more pairs of nucleotides are removed from a gene

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Deletion (chromosomal)

A chromosomal mutation that involves the loss of all or part of a chromosome

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Translocation

The process in which a segment of a chromosome breaks off and attaches to another chromosome.

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Inversion

A genetic mutation in which the order of a segment of genetic material is reversed.

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Insertion

A mutation involving the addition of one or more nucleotide pairs to a gene.

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Frameshift mutation

mutation that shifts the "reading" frame of the genetic message by inserting or deleting a nucleotide

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Operon

group of genes operating together

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Operator site

site where a DNA binding protein can bind to DNA

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TATA box

a short region of DNA before the start of a gene; used in eukaryotic gene expression

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Transcription factors

A regulatory protein that binds to DNA and affects transcription of specific genes.

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Hox genes

series of genes that controls the differentiation of cells and tissues in an embryo

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Polyploidy

condition in which an organism has extra sets of chromosomes

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Genes

DNA segments found on chromosomes that carry genetic information to determine protein synthesis.

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Study Notes

DNA, RNA, and Protein Synthesis

  • Griffith: Discovered bacterial transformation studying pneumonia in mice.
  • Avery: Determined DNA was the genetic material, building on Griffith's work.
  • Hershey and Chase: Used radioactive isotopes (sulfur-35 and phosphorus-32) to label DNA and proteins in bacteriophages, proving DNA carries genetic information.
  • Sulfur-35: Radioactive isotope used to label proteins.
  • Phosphorus-32: Radioactive isotope used to label DNA.
  • Bacteriophage: A virus that infects bacteria.
  • Chargaff's Rule: A = T, and C = G; the amounts of adenine and thymine bases are equal and the amounts of cytosine and guanine bases are equal in DNA.
  • Nucleotide: The building block of DNA; made of a sugar, a phosphate group, and a nitrogenous base.
  • Nitrogenous Bases: Adenine (A), Guanine (G), Cytosine (C), and Thymine (T) (or Uracil in RNA).
  • Hydrogen Bonds: Weak bonds that hold base pairs together in DNA.
  • Phosphate: Forms the backbone of the DNA strand, linked to the deoxyribose sugar.
  • Deoxyribose: A five-carbon sugar in DNA.
  • Rosalind Franklin: Provided crucial X-ray diffraction images of DNA that Watson and Crick used to develop their double helix model.
  • Watson and Crick: Developed the double helix model of DNA structure.
  • Histones: Proteins around which DNA is tightly coiled in eukaryotic cells, forming nucleosomes.
  • Nucleosome: A structural unit of eukaryotic chromatin; DNA wound around histone proteins.
  • Helicase: An enzyme that unwinds the DNA double helix during replication.
  • Replication Fork: The Y-shaped region where DNA strands separate during replication.
  • DNA Polymerase: Enzyme that adds nucleotides to a DNA strand during replication and proofreads the DNA during replication.
  • RNA: A single-stranded nucleic acid containing ribose sugar and uracil instead of thymine.
  • mRNA (messenger RNA): Carries genetic information from DNA in the nucleus to the ribosome for protein synthesis.
  • tRNA (transfer RNA): Carries amino acids to the ribosome during protein synthesis, based on the mRNA codon.
  • rRNA (ribosomal RNA): Forms part of the ribosome, the site of protein synthesis.
  • Telomere: Repeating nucleotide sequences at the ends of chromosomes; protect genes from loss during replication.
  • Telomerase: Enzyme that maintains telomere length.
  • Transcription: The process of making RNA from a DNA template.
  • Translation: The process of making a protein from an mRNA template.
  • Codon: A sequence of three nucleotides that codes for a specific amino acid.
  • Promoter: Region of DNA where RNA polymerase binds to initiate transcription.
  • Introns: Non-coding regions of DNA within a gene.
  • Exons: Coding regions of DNA within a gene that are expressed.
  • Point Mutation: A single nucleotide change in the DNA sequence.
  • Duplication Mutation: A segment of DNA is copied multiple times.
  • Substitution Mutation: One nucleotide is replaced by another.
  • Deletion Mutation: One or more nucleotides are removed from the DNA sequence.
  • Deletion (chromosomal): A segment of a chromosome is lost.
  • Translocation: A segment of one chromosome moves to another chromosome.
  • Inversion: A segment of a chromosome is reversed.
  • Insertion Mutation: One or more nucleotides are added to the DNA sequence.
  • Frameshift Mutation: An insertion or deletion that shifts the reading frame (codon groups) during translation, often causing protein dysfunction.
  • Operon: A group of genes that are regulated together.
  • Operator Site: The region on DNA where a regulatory protein can bind to control gene expression.
  • TATA Box: A DNA sequence in eukaryotes that is a common promoter site.
  • Transcription Factors: Regulatory proteins that bind to DNA and influence the transcription of specific genes.
  • Hox Genes: Genes that control the body plan of an embryo.
  • Polyploidy: Having extra sets of chromosomes.
  • Genes: Segments of DNA that contain the code for proteins. Found on chromosomes.

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Description

This quiz covers key concepts of DNA, RNA, and the processes involved in protein synthesis. Explore the experiments of Griffith, Avery, and Hershey and Chase, and understand the significance of Chargaff's Rule and the structure of nucleotides. Test your knowledge on the molecular biology of genetics!

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