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Biology Ch. 10.4-13

TermDefinition
RNA- natural polymer that is present in all living cells and that plays a role in protein synthesis.
Transcription- the process of forming a nucleic acid by using another molecule as a template; particularly the process of synthesizing RNA by using one stand of a DNA molecule as a template.
translation- the portion of protein synthesis that takes place at ribosomes and that uses the codons in mRNA molecules to specify the sequence of amino acids in polypeptide chains.
protein synthesis- he formation of proteins by using information contained in DNA and carried by mRNA.
ribose- a five carbon sugar present in RNA
mRNA- a single stranded RNA molecule that encodes the information to make a protein
rRNA- an organelle that contains most of the RNA in the cell and that is responsible for ribosome function.
tRNA- a RNA molecule that transfers amino acids to the growing end of a polypeptide chain during translation
RNA polymerase- an enzyme that starts the formation of RNA by using a strand of DNA molecule as a template
promoter- a nucleotide sequence on a DNA molecule to which an RNA polymerase molecule binds which initiates the transcription of a specific gene
termination signal- a specific sequence of nucleotides that marks the end of a gene
genetic code- the term for the rules that relate how a sequence of nitrogenous bases in nucleotides corresponds to a particular amino acid.
Codon each three-nucleotide sequences in mRNA that encodes an amino acid or signifies a start or stop signal.
Anticodon three nucleotides on the RNA that are complementary to the sequences of a codon in mRNA.
Genome the complete genetic content.
Sex chromosome genes that determine the sex of an individual.
Autosome Remaining chromosomes that are not directly involved in determining the sex of an individual.
Sex linked trat refers to a trait that is coded for by an allele on a sex chromosome
Linked gene genes that tend to be inherited together
Chromosome map a diagram that shows the linear order of genes on a chromosome.
Map unit a crossing-over of 1 percent
germ cell mutation occurs in an organism’s gametes
Somatic-cell mutation- take place in an organism’s body cells and can therefore affect the organism
Lethal mutation cause death often before birth.
Deletion the loss of a piece of a chromosome due to breakage
Inversion a chromosomal segment breaks off flips around backward and reattaches
Translocation a piece of one chromosome breaks off and reattaches to a nonhomologous chromosome
Nondisjunction- a chromosome fails to separate from its homologue during meiosis
Point mutation- the substitution, addition, or removal of a single nucleotide.
Substitution- one nucleotide replaces another
Frame shift mutation- loss which can cause incorrect grouping of remaining codons.
Insertion Mutation - one or more nucleotides are added to a gene, which can also result in a frameshift mutation
Pedigree- a diagram that shows how a trait is inherited over several generations
Carrier individuals such as the four people in the fifth generation.
Genetic disorder diseases or disabling conditions that have a genetic basis
Polygenic characteristics influenced by several genes
Complex character characters that are influenced strongly both by the environment and by genes
Multiple allele genes with three or more alleles.
Codominance- both alleles are expressed in the phenotype of a heterozygote.
Incomplete dominance- A trait that is intermediate between the two parents.
Sex-influenced trait- involved in other complex characters
Huntington’s disease- an autosomal dominant condition characterized by forgetfulness and irritability.
Amniocentesis- allows a physician to remove some amniotic fluid from the amnion between the 14th and 16th week of pregnancy
Chorionic villi sampling- a physician takes samples of the chorionic villi between the 8th and 10th week.
Genetic counseling- the process of informing a person or couple about their genetic makeup.
gene therapy a technique that places a healthy copy of a gene into the cells of a person whose copy of the gene is defective.
Created by: makenzi_au
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