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DNA
science 2.3
Term | Definition |
---|---|
Deoxyribonucleic acid | carrier of genetic information |
Nucleotide | what a molecule of DNA is made up of |
Thymine | Adenine |
Cytosine | Guanine |
Double Helix | the structure formed by double-stranded molecules of nucleic acids such as DNA |
What nucleotides are made up of | Phosphate, Sugar, Nitrogenous base |
Codon | bases that are arranged in triplets |
Helicase | separates the two strands |
DNA Polymerase | adds nucleotides to each strand . binds to the primer |
Leading Strand | 5' to 3' direction |
Lagging Strand | 3' to 5' direction |
Primase | an enzyme that adds an RNA primer on a specific location of the lagging strand |
Okazaki fragments | how polymerase adds nucleotides to lagging strands |
Mutations | a change in the DNA of a cell |
Gene Mutation | one gene is affected/ mutated |
Point Mutation | one nucleotide is substituted for another |
Frameshift Mutation | the insertion or deletion of a nucleotide in the sequence |
Mutagen | anything that causes mutation |
Deletion | involves the loss of a piece of chromosome or a break of the DNA molecule |
Inversion | when a part of the DNA segment within the chromosome change in direction |
Chromosomal Mutation | involves the entire chromosome affecting many genes |
Translocation | when a piece of one chromosome moves to a nonhomologous reciprocal chromosome |
Duplication | when gene sequences have been repeated several too many times |
Chromosomes | carry genes that transmit hereditary traits from parent to offspring |
XX | Female |
XY | Male |
Aneuploidy | the most common chromosome abnormality. extra or lacking chromosome |