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PBS Unit 2.2 Vocab

TermDefinition
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.
Created by: Jaden John
 

 



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