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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 |