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78 Cards in this Set
- Front
- Back
the impact of a single gene on more than one characteristic
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pleiotropy
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a molecule carrying DNA from more than one source
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recombinant DNA (transgenic organism)
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States that genes are located on chromosomes and that the behavior of chromosomes during meiosis and fertilization accounts for inheritance patterns.
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chromosome theory of inheritance
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the enzymes that make the covalent bonds between the nucleotides of a new DNA strand
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DNA polymerases
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the transfer of genetic info from DNA into an RNA molecule
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transcription
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the transfer of genetic info in the RNA into a protein
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translation
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small, circular DNA molecules that are separate from the much larger bacterial chromosome
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bacterial plasmids
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DNA carriers that move genes from one cell to another
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vectors
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a technique by which any segment of DNA can be amplified (cloned)
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polymerase chain reaction (PCR)
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a method for sorting macromolecules - proteins or nucleic acids - primarily on the basis of their electrical charge and length
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gel electrophoresis
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human chromosomes contain how many genes?
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3.2 billion nucleotide pairs of DNA and 30,000 to 40,000 genes
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Fertilization of one plant by pollen from a different plant
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cross-fertilization
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varieties for which self-fertilization produced offspring all identical to the parent
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true-breeds
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the offspring of two different true-breeding varieties
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hybrids
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pairs of alleles segregate (separate) during gamete formation; the fusion of gametes at fertilization creates allele pairs again
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Mendel's principle of segregation
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when an orgaism has a pair of identical alleles for a gene
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homozygous
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when an organism has two different alleles for a gene
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heterozygous
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each pair of alleles segregates independently of the other pairs during gamete formation
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Mendel's principle of independent assortment
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chromosomes other than the sex chromosomes
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autosomes
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hybrids that have an appearance in between the phenotypes of the two parents
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incomplete dominance
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How does codominance differ from incomplete dominance?
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codominance is the expression of both alleles; incomplete dominance the expression of one intermediate trait
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The DNA-containing structures that carry the organism's genes.
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chromosomes
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A complete set of an organism's genes. (Humans have around 35,000 genes.) Located on chromosomes in the cell nucleus.
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genome
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A combination of DNA and protein molecules.
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chromatin
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Consists of DNA wound around a protein core of eight histone molecules.
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nucleosome
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Each chromosome consists of two copies of these before beginning division.
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sister chromatids
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A typical body cell, has 46 chromosomes in humans.
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somatic cell
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The two chromosomes of a matching pair.
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homologous chromosomes
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All body cells in an organism contain two homologous sets of chromosomes.
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diploid organism
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A cell with a single chromosome set.
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haploid cell
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egg and sperm cells
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gametes
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An exchange of genetic material - pieces of chromosomes - between homologous chromosomes, occurs during the first prophase of meiosis.
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crossing over
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These chromosome are called _______ because they result from genetic recombination, the production of gene combinations different from those carried by the parental chromosomes.
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recombinant (chromosomes)
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trisomy 21
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Down's syndrome
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The members of a chromosome pair fail to separate at anaphase.
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nondisjunction
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XXY
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Klinefelter syndrome (male)
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XO
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Turner syndrome (female)
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Organism that has more than two sets of homologous chromosomes in each somatic cell.
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polyploid
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the organs that produce gametes
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gonads
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Cells with the potential to give rise to every type of cell in the body.
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stem cells
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In "The Origin of Species," (1859) Charles Darwin proposed that:
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1. Modern species descended from ancestral species (descent with modification) and 2. natural selection is the mechanism of evolution.
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The idea that a population of organisms can change over the generations if individuals having certain heritable traits leave more offspring than other individuals.
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natural selection
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How old is the earth?
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3.5 billion years old
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The comparison of body structures between different species.
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comparative anatomy
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similarity due to common ancestry
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homology
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the comparison of structures that appear during the development of different organisms
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comparative embryology
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consists of all alleles in all the individuals making ap a population
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gene pool
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What produces genetic variation?
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mutations and sexual recombination
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a general formula for calculating the frequencies of genotypes in a gene pool from the frequencies of alleles, and vice versa
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Hardy-Weinberg formula
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A nonevolving population is in genetic equilibrium, also called
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Hardy-Weinberg equilibrium
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Evolution is a generation-to-generation change in a population's frequencies of alleles. Because this describes evolution on the smallest scale, it is sometimes referred to as ______
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microevolution
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a change in the gene pool of a small population due to chance
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genetic drift
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Genetic drift due to a drastic reduction in population size
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the bottleneck effect
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Genetic drift occurs when a few individuals colonize a new habitat. The smaller the colony, he less its genetic makeup will prepresent the gene pool of the larger population from which the colonists emigrated. Genetic drift in a new colony is called _____
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the founder effect
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Apopulation may gain or lose alleles by ____, or genetic exchange between two populations
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gene flow
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the contribution an individual makes to the gene pool of the next generation relative to the contributions of other individuals
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Darwinian fitness
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a change in life-forms noticeable enough to be evident in the fossil record
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macroevolution
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a population or group of populations whose members have the potential to interbreed with one another in nature to produce fertile offspring
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species
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the origen of new species
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speciation
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domain > kingdom > phylum > class > order > family > genus > species
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taxonomic hierarchy
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both DNA and RNA are nucleic acids which consist of long chains (polymers) of units called
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nucleotides
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DNA and RNA nucleotides are joined by covalent bonds between the sugar of one nucleotide and the phosphate of the next. What is this called?
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sugar-phosphate backbone
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Each nucleotide of DNA or RNA consists of what three components?
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a nitrogenous base, a sugar (deoxyribose, ribose), and a phosphate group
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two polynucleotide strands of DNA
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double helix
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The genetic instructions for the amino acid sequence of a polypeptide chain are written in DNA and RNA as a series of three-base words called
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codons
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RNA nucleotides are linked by the transcription enzyme called
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RNA polymerase
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The nucleotide sequence that says "start transcribing" that the RNA polymerase attaches to is called
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a promoter
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Phase 1 of transcription; the attachment of RNA polymerase to the promoter and the start of RNA synthesis is called
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initiation
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phase 2 of transcription; the RNA grows longer and peels away from its DNA template, allowing the two separated DNA strands to come back together in the region already transcribed
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elongation
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phase 3 of transcription; the RNA polymerase reaches a special sequence of bases in the DNA template called a terminator.
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termination
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the sequence of bases in the DNA template that signals the end of transcription
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terminator
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RNA translation yields
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a polypeptide of amino acids
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what are the two types of mutations?
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base substitutions and base insertions or deletions
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Viruses that attack bacteria are called
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bacteriophages, or phages
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A reproduction cycle of a virus that uses the cell's machinery to produce copies of the virus. The cell lyses, or breaks open.
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lytic cycle
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A virus cycle; the virus DNA inserts by genetic recombination into the bacterium's DNA. The prophage DNA replicates along with the host cell DNA.
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lysogenic cycle
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Once inserted into the bacterial chromosome, the phage (virus) DNA is called a
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prophage
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The synthesis of DNA on an RNA template
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reverse transcriptase
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