click below
click below
Normal Size Small Size show me how
PBS Unit 2.2 Vocab
| Term | Definition |
|---|---|
| alleles | Different versions of the same gene that determine variations of a trait. |
| autosomes | Chromosomes that are not sex chromosomes; humans have 22 pairs. |
| Centromere | The region of a chromosome that holds sister chromatids together. |
| chromatid | One identical half of a duplicated chromosome. |
| chromosome | A structure made of DNA and proteins that carries genetic information. |
| deletion mutation | A mutation in which one or more nucleotides are removed from DNA. |
| DNA | Deoxyribonucleic acid; the molecule that stores genetic instructions for living organisms. |
| DNA Primer | A short strand of nucleic acid that provides a starting point for DNA replication. |
| dominant allele | An allele that is expressed whenever it is present, even if only one copy exists. |
| eukaryotic | Cells that contain a nucleus and membrane-bound organelles. |
| Familial Hypercholesterolemia | An inherited disorder causing high cholesterol due to a genetic mutation affecting LDL receptors. |
| frameshift mutation | A mutation caused by insertion or deletion that shifts the reading frame of DNA. |
| gene | A segment of DNA that codes for a protein or trait. |
| genome | The complete set of genetic material in an organism. |
| genotype | The genetic makeup or allele combination of an organism. |
| gel electrophoresis | A laboratory technique used to separate DNA fragments based on size using an electric current. |
| heterozygous | Having two different alleles for a gene. |
| homologous chromosomes | Chromosome pairs with the same genes, one inherited from each parent. |
| homozygous | Having two identical alleles for a gene. |
| insertion mutation | A mutation in which extra nucleotides are added into DNA. |
| karyotype | An organized image or display of an individual’s chromosomes. |
| Messenger RNA (mRNA) | RNA that carries genetic instructions from DNA to ribosomes for protein production. |
| mitosis | Cell division producing two genetically identical daughter cells. |
| mutation | A change in the DNA sequence. |
| nondisjunction | Failure of chromosomes to separate properly during cell division. |
| nucleotides | The building blocks of DNA and RNA consisting of a sugar, phosphate group, and nitrogenous base. |
| pedigree | A chart used to track inheritance of traits through generations. |
| phenotype | The observable physical traits of an organism. |
| point mutation | A mutation affecting a single nucleotide base pair. |
| polymerase chain reaction | A technique used to make many copies of a DNA segment. |
| protein | A molecule made of amino acids that performs cellular functions and determines traits. |
| protein synthesis | The process of making proteins using DNA instructions through transcription and translation. |
| punnett square | A diagram used to predict genetic trait outcomes from parental crosses. |
| recessive allele | An allele expressed only when two copies are present. |
| restriction enzyme | A protein that cuts DNA at specific sequences. |
| ribonucleic acid (RNA) | A nucleic acid involved in protein synthesis and gene expression. |
| sex chromosomes | Chromosomes that determine biological sex (X and Y in humans). |
| silent mutation | A mutation that does not change the amino acid or protein produced. |