STRUCTURE AND FUNCTION OF DNA

Cards (26)

  • DNA and RNA Structure
    Both DNA and RNA are nucleic acids, which consists of long chains (polymers) of chemical units (monomers) called nucleotides.
  • DNA and RNA Structure
    Nucleotides are joined together by covalent bonds between the sugar of one nucleotide and the phosphate of the next.
    • This results in a repeating pattern of sugar-phosphate, which is known as sugar-phosphate backbone.
  • DNA and RNA Structure
    Each nucleotide consists of three components:
    • a nitrogenous base
    • a sugar (blue)
    • a phosphate group
  • DNA and RNA Structure
    The four nucleotides found in DNA differ only in their nitrogenous bases. The bases can be divided into two types:
    SINGLE RING STRUCTURES:
    • Thymine T
    • Cytosine C
    DOUBLE RING STRUCTURES:
    • Adenine A
    • Guanine G
  • DNA and RNA Structure
    Instead of thymine, RNA has a similar base called uracil U.
  • DNA and RNA Structure
    For DNA, the sugar is called deoxyribose because, compared with sugar ribose. it is missing an oxygen atom.
    DNA - deoxyribonucleic acid where nucleic referring to DNA's location in the nuclei of eukaryotes
  • DNA and RNA Structure
    For RNA, it contains a slightly different sugar than DNA (ribose instead of deoxyribose, accounting for the names RNA versus DNA).
  • DNA and RNA Structure
    RNA and DNA polynucleotides have the same chemical structure
  • Watson and Crick's Discovery of the Double Helix
    Watson and Crick worked out the three-dimensional structure of DNA: two polynucleotide strands wrapped around each other in a double helix.
    • hydrogen bonds between bases hold the strands together
    • Each base pairs with a complementary partner: A&T, G&C
  • DNA Replication
    The structure of DNA, with its complementary base pairing, allows it to function as the molecule of heredity through DNA replication.
  • DNA Replication
    The two strands of parental DNA separate, and each becomes a template for the assembly of a complementary strand from a supply of free nucleotides.
  • DNA Replication
    The nucleotides are lined up one at a time along the template strand in accordance with the base-pairing rules.
    • Enzymes link the nucleotides to form new DNA strands.
    • The completed new molecules, identical to the parental molecule, are known as daughter DNA molecules
  • DNA Replication
    DNA polymerases are the enzymes that make the covalent bonds between the nucleotides of a new DNA strand.
    • As an incoming nucleotide base-pairs with its complement on the template strand, a DNA polymerase adds it to the end of the growing daughter strand.
  • The Central Dogma: From DNA to RNA to Protein
    How an Organism's Genotype determines its Phenotype?
    • The information constituting an organism's genotype is carried in the sequence of its DNA bases.
    • The genotype controls phenotype through the expression of proteins.
  • How an Organism's Genotype determines its Phenotype?
    DNA specifies the synthesis of proteins. However, a gene does not build a protein directly.
    • Instead, DNA dispatches instructions in the form of RNA, which in turn programs protein synthesis.
  • How an Organism's Genotype determines its Phenotype?
    The molecules "chain of command" is from DNA in the nucleus to RNA to protein synthesis in the cytoplasm.
  • How an Organism's Genotype determines its Phenotype?
    Replication - the process by which DNA makes a copy of itself during cell division.
  • How an Organism's Genotype determines its Phenotype?
    The two stages are:
    1. Transcription - the transfer of genetic information from DNA to an RNA molecule.
    2. Translation - the transfer of the information from RNA into a polypeptide (protein strand)
    3. The start codon marks the site at which translation into protein sequence begins,
    4. AUG - the start codon
    5. UGA, UAA, UAG - stop codons
  • How an Organism's Genotype determines its Phenotype?
    The function of a DNA gene is to dictate the production of a polypeptide.
  • Nucleotides to Amino Acids
    The DNA of a gene is transcribed into RNA using the usual base-pairing rules, except that an A in DNA pairs with U in RNA.
  • Nucleotides to Amino Acids
    In the translation of a genetic message, each triplet of nucleotide bases in the RNA, called a codon, specifies one amino acid in the polypeptide.
  • The Genetic Code
    In addition to codons that specify amino acids, the genetic code has one codon that is a start signal and three that are stop signals for translation.
  • Transcription: From DNA to RNA
    RNA polymerase binds to the promoter of a gene, opens the DNA double helix there, and catalyzes the synthesis of an RNA molecule using one DNA strand as a template.
    As the single-stranded RNA transcript peels away from the gene, the DNA strands rejoin.
  • The Processing of Eukaryotic RNA
    The RNA transcribed from a eukaryotic gene is processed before leaving the nucleus to serve as messenger RNA (mRNA). Introns are spliced out, and a cap and tail are added.
  • Translation: The Process
    There are three steps of translation:
    Initiation - a ribosome assembles with the mRNA and the initiator tRNA bearing the first amino acid
    Elongation - at the start codon, the codons of the mRNA are recognized one by one by tRNA's bearing succeeding amino acids.
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    The ribosome bonds the amino acids together. With each addition, the mRNA moves by one codon through the ribosome
    Termination - when a stop codon is reached, the completed polypeptide is released
  • Summary of Central Dogma
    DNA --> RNA --> Protein