DNA is a complex molecule containing the genetic information that makes up the chromosomes.
RNA is a single-stranded nucleic acid that passes along genetic messages.
DNA provides living organisms with guidelines—genetic information in chromosomal DNA—that help determine the nature of an organism's biology.
DNA consists of two long chains of nucleotides twisted into a double helix and joined by hydrogen bonds between the complementary bases adenine and thymine or cytosine and guanine.
DNA has two main roles: protein synthesis and replication.
A nucleotide is the monomer of nucleic acids made up of a 5-carbon sugar, a phosphate group, and a nitrogenous base.
Deoxyribonucleic acid (DNA) is a type of nucleic acid.
Purines include Adenine and Guanine.
Pyrimidines include Cytosine and Thymine & uracil.
Hydrogen bonds hold the two DNA strands together (between the nitrogenous bases).
The backbone of DNA is made up of a phosphate group and deoxyribose.
Semi-conservative replication means that in each new DNA double helix, one strand is from the original molecule, and one strand is new.
DNA replication is the process in which DNA makes a duplicate copy of itself.
DNA polymerase is the enzyme responsible for replicating DNA — for using a template strand to construct a complimentary sequence of nucleotides, creating a double-stranded DNA molecule.
DNA polymerase can also proofread the new strand as it is created and is involved in repairing DNA damage and mutations.
Genes are the biochemical units of heredity that make up the chromosomes; a segment of DNA capable of synthesizing a protein.
Initiation: DNA helicase unwinds the double helix, creating a replication fork.
Tumor suppressor genes: A gene whose protein product inhibits cell division, thereby preventing the uncontrolled cell growth that contributes to cancer.
Point mutation: A different amino acid - the location of the amino acid changed will impact the scale of the changes.
Negative cell-cycle regulatory proteins: Proteins that halt the cell cycle.
Frameshift mutations: Caused by insertions or deletions - NOT POINT MUTATIONS.
Silent mutation: A mutation that changes a single nucleotide, but does not change the amino acid created.
Elongation: DNA polymerase adds complementary nucleotides to the template strands, synthesizing new DNA strands.
DNA is read 5' to 3'.
DNA ligase joins the Okazaki fragments on the lagging strand, completing the replication process.
Conditional mutations: A mutation that results in a characteristic phenotype only under certain environmental conditions.
Nonsense mutation: Converts a sense codon (like the 3 bases which pair with an amino acid) to a stop codon (nonsense codon).
Checkpoints and cancer: S-phase checks that DNA replication was proper.
Gene mutation: A change in the sequence of the bases in a gene, which changes the structure of the polypeptide that the gene codes for.
Missense mutation: A nucleotide-pair substitution that results in a codon that codes for a different amino acid (a base gets changed creating a different amino acid).
Cancer: Any malignant growth or tumor caused by abnormal and uncontrolled cell division.
Termination: 3rd step of DNA replication.
Oncogenes: Genes that cause cancer by blocking the normal controls on cell reproduction.
Positive cell-cycle regulatory proteins: Progress the cell cycle - when these become oncogenes, this would lead to cancerous spreading.
During translation, the mRNA docks with the ribosome (also known as rRNA) at the AUG or methionine codon.
A tRNA (called transfer RNA) is a structure who has an anticodon that pairs with a specific codon on the mRNA.
The first tRNA moves into the A-site of the ribosome.
The e site of the ribosome holds the tRNA that carries the growing polypeptide chain.
The A site of the ribosome holds the tRNA that carries the next amino acid to be added to the chain.
During the process of transcription, a DNA template strand is used to make mRNA using RNA Polymerase.