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72 Cards in this Set
- Front
- Back
Allele |
One of two or more alternative forms of a gene that arise by mutation and are found at the same place on a chromosome |
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Allele series |
the different mutant alleles of a gene that case a range of phenotypes |
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Ascus |
the sack that forms after meiosis in yeast that contains all 4 haploid spores produced |
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Asexual reproduction |
When a single organism reproduces and the offspring inherits genes from only that parent |
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Autosomal |
A chromosome whose number does not differ between sexes |
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Auxotroph |
A living that requires additional nutrients to grow due to at least one faulty pathway |
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Blended Inheritance |
An offspring expresses a phenotype that is in between the 2 homozygous traits of its parents |
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Breeding True |
Self fertilization produces only offspring with the same trait |
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centiMorgan |
unit used in genetic mapping derived from probability |
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Chi-Squared Analysis |
a statistical method for testing the probability that the null hypothesis is true |
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Chiasmata |
a point at which paired chromosomes remain in contact and crossing over occurs |
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chromatid |
one identical half of a chromosome |
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chromosome |
the part of the cell that holds the genetic transcript of the organism |
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codominance |
expressing characteristics equally of both parents for a single trait |
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coefficient of coincidence |
the measure of interference in the formation of chromosomal crossover during meiosis |
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Complementation Test |
a cross done to determine if two recessive mutations are allelic |
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crossing over |
homologous chromosomes exchange segments of genetic material to form recombinant chromosomes |
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dipolid |
having two sets of haploid homologous chromosomes |
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dihybrid cross |
a genetic cross between parents that differ in two characteristics controlled by genes at different loci |
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ditype |
a tetrad type containing two different genotypes, both of which are parental |
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dominant |
property of an allele that completely controls the phenotype regardless of whether the individual is homozygous or heterozygous for that allele |
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duplicate genes |
2 loci encode for the same funcion |
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epistasis recessive |
the phenotype is controlled by B which masks A. Additionally, a homozygous recessive b will mask any dominant A allele. |
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Epistasis dominant |
the phenotype is controlled by B which masks A where any dominant B allele masks any A, despite its dominance |
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expressivity |
the extent or degree to which the phenotype is expressed in each individual |
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incomplete dominance |
when the inherited phenotype of a heterozygote is intermediate between those of the two homozygotes |
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interference |
a situation where the number of observed double crossover events is less that what is predicted by the frequencies of a single crossover event |
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gamete |
a cell that joins together to begin making an organism |
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gene |
a (hypothetical) unit or object of inheritance |
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hypothesis |
a proposed explanation that is consistent with the known limited evidence, therefore is not simply accepted and must be tested
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genotype |
all or part of the genetic constitution of an individual |
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haploid |
having a single set of unpaired chromosomes |
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haploinsufficient |
when a diploid organism has only a single functional copy of a gene and can not produce enough gene product for a wild-type phenotype |
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hemizygous |
having only 1 allele for a particular locus |
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heterogametic sex |
forming two types of gametes which one produces male offspring and the other female offspring |
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heterozygous |
when an organism possesses more than one distinct alleles for one trait |
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homogametic sex |
forming gametes which all have the same type of sex chromosome |
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homozygous |
when all of an organism's alleles for a trait are identical |
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hypomorphic allele |
an allele that reduces but does not eliminate a product's functionality |
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independent assortment |
during gamete formation, the segregation of one pair of genes is independent of other gene pairs |
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linkage groups |
a set of genes at different loci on the same chromosome that, except for crossing over, tend to act as a single pair of genes in meiosis instead of undergoing independent assortment |
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linked genes |
genes found on the same chromosome that do not assort independently of one another |
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mapping function |
a visual representation of gene placement on a chromosome |
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meiosis |
cell division that results in 4 daughter cells each with half the number of chromosomes as the parent cell |
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mutation |
a permanent change in genetic code |
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neomorphic allele |
an allele that produces an altered product with a completely different function than the wild type |
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null allele |
an allele that makes a completely nonfunctional product |
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mitosis |
cell division that results in two daughter cells that have the same number and kind of chromosomes as the parent cell |
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null hypothesis |
a statement that says that the difference between observed and expected values is due to change alone |
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partial dominance |
a phenotype of a heterozygote is intermediate between those of two homozygotes |
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pedigree |
a diagramed representation used to follow heritable characteristics through bloodlines |
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penetrance |
a binary case where a fraction of individuals with a given genotype show an associated phenotype |
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phenotype |
the set of observable characteristics of an individual resulting from the interaction of its genotype with its environment |
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poisson distribution |
the probability of independent events occurring within a fixed amount of time |
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product law of probability |
probability of events occurring together is the product (multiply) of their individual probabilities |
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prototroph |
an organism that has all of the metabolic pathways required to survive given initial nutrients |
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punnett square |
a diagram that uses each gamete possibility to determine possible genotypic outcomes of offspring |
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recessive |
property of an allele in which the trait is only seen in homozygous individuals and not heterozygous individuals |
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reciprocal cross |
breeding experiment designed to test the role of parental sex on a given inheritance pattern using true breeding parents |
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recombination |
the formation of nonparental combination of genes in a gamete or individual |
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recombination frequency |
the probability of recombination occurring |
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redundant genes |
the same function is encoded by two or more genes |
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segregation of allele pair |
when chromosomes (or sister chromatids) move to opposite sides of the cell to divide into individual daughter cells |
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sex linkage |
a gene that is on a sex chromosome and therefore linked to it |
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sexual reproduction |
two separate individuals produce gametes in meiosis that come together to form a zygote |
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sister chromatid |
one half of a chromosome that contains identical genetic information to its counterpart |
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suppression |
gene B prevents the expression of gene A |
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synthetic phenotype |
when a double mutant (involving 2 distant loci) has a phenotype distinct from either single mutant homozygote |
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testcross |
a test cross is crossing an individual homozygous recessive for a trait with an individual of unknown genotype to determine the unknown genotype |
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tetrad |
the sack that forms after meiosis in yeast that contains all 4 haploid spores produced |
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tetratype |
tetrad containing 4 different genotypes, two parental and two recombinant |
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wild-type allele |
the allele that occurs most commonly in nature for a given gene |