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87 Cards in this Set
- Front
- Back
most common recent ancestor (MCRA) |
share closest connected node |
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tRNA |
carries individual amino acids to ribosomes to make protein |
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rRNA |
helps make up ribosomes
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ribosome |
organelle in cytoplasm - synthesizes proteins |
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genetic code |
translation of codons to amino acids |
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phospholipid |
derivatives with 2 hydrophobic fatty acids and a hydrophilic phosphate group (makes up bilayers) |
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carbohydrate |
source of energy and structure, made of sugars, C, H, O: 1:2:1 |
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allele |
different variations of a gene - from mutations |
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binary fission |
division of prokaryotic cells |
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centromere |
holds together sister chromatids |
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chiasmata |
crossover parts of bivalents with sister chromatids |
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cytokinesis |
division of cell cytoplasm |
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diploid |
2 complete sets of chromosomes (human somatic cells) |
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haploid |
1 complete set of chromosomes (human germ cells) |
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homologous chromosomes |
not sex chromosomes; one from father, one from mother |
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interphase |
part of cell cycle: G1, S, G2; preparation for cell division |
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M-phase |
part of cell cycle, parent cell divides into 2 daughter cells, mitosis and cytokinesis
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meiosis |
division of sex cells, results in 4 daughter cells, half the chromosomes, daughter cells unique |
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metaphase |
spindle complete, chromosomes line up |
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mitosis |
division of cell nucleus |
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non-disjunction |
failure of chromosomes/chromatids to separate properly during cell division |
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recombination |
rearrangement of genetic material especially crossing over |
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S-phase |
synthesis, replication of DNA between G1 and G2 |
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sister chromatids |
duplicated chromosomes connected to parent after S-phase, genetically identical |
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zygote |
2 gametes come together and fuse, result of fertilization |
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backcross |
crossing hybrid with parent of genetically similar to parent |
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F1/F2 |
First offspring/F1 offspring
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genotype |
genetic makeup |
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hybridization |
interbreeding between 2 different varieties of a species or organism |
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nonsense mutation |
creates stop codon |
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nonsynonymous (missense) mutation |
results in amino acid replacement (point mutation) |
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phenotype |
observable characteristics or traits |
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polymorphism |
genetic difference among individuals common so that it is probably in a group of 50 individuals |
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reciprocal crosses |
expression of trait male and female parents interchanged |
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segregate |
formation of gametes - half get one allele and half get other allele |
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synonymous (silent) mutation |
does not change amino acid for codon |
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testcross |
cross of unknown genotype with homozygous recessive genetype |
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true-breeding |
phenotype of each offspring identical to previous |
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translocation |
one part of a chromosome breaks off and attaches to another |
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codominance |
both alleles are dominant |
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dihybrid cros |
cross between 2 pure lines that differ in 2 observed traits |
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incomplete dominance |
phenotype of heterozygous is between the two homozygous genetopes |
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independent assortment |
two different traits are not dependent on each other
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mitochondrial inheritance |
transmission of mitochondrial inheritance from parent to child |
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maternal inheritance |
traits passed down from mother to child |
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pedigree |
diagram of family genetic history |
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segregation |
during meiosis each gamete receives either maternal or paternal gene |
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autosome |
chromosome that is not a sex chromosome |
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epistasis |
genes that modify the expression of other genes |
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genetic distance |
measure of genetic divergence |
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linkage |
genes transmitted together in inheritance - don't sort independently |
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linkage mapping |
map of genes in terms of recombination frequency |
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non-recombinant type |
allele present in same combination as in the parents |
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pleiotropy |
one gene effects multiple seemingly unrelated pheonotropic traits |
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reciprocal cross |
pair of crosses between male of one strain, female of another strain, and vice versa |
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recombinant type |
result of a crossover |
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recombination |
crossing over of chromosomes |
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sex-linkage |
genes located on the sex chromosome |
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analogous |
similarities due to independent adaptation by different species |
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ancestral trait |
trait shared by a group of organisms as a result of descent from a common ancestor |
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convergent evolution |
independent evolution of similar features in species of different lineages
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derived trait |
traits existent in a present organism not present in their ancestors |
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fitness |
measure of the extent to which an individual's genotype is represented in the next generation |
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homologous |
characters that are similar because of descent from a common ancestor |
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monophyletic group |
all share an ancestor not shared with any other species |
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parsimony |
choosing the simpler hypothesis for a given set of observations |
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polytomy |
an unresolved pattern of divergence, a node with multiple branches
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sister taxa |
share a MRCA, more closely related to each other than to any other group |
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shared derived trait (synapomorphy) |
homology shared by some, but not all members of the group |
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allele frequency |
number of alleles present in the population divided by the total number of alleles
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allele fixation |
all genes contain a particular allele |
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balancing natural selection |
maintain 2 or more alleles in a population, maintain an allele between 0% and 100% (sickle cell) |
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continuous (polygenic) trait |
variation occurs along a spectrum |
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discrete trait |
clear alternative states (yellow/green peas) |
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directional natural selection |
leads to a change in the trait over time, level of variation is the same |
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disruptive natural selection |
in favor of extremes and against intermediates, mean stays the same, variability increases or stays the same |
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genotype by environmental interactions |
phenotype result of interplay of genes and the environment
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heritability |
proportion of total variation in the trait that is due to genetic differences among individuals |
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heterozygote advantage |
heterozygote fitness higher than either homozygote |
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polygenic (quantitative) inheritance |
when many genes and environment affect a trait |
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positive selection |
increases the frequency of a favorable gene |
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relative fitness |
fitness of a genotype divided by fitness of maximum genotype |
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negative selection |
decreases the frequency of a harmful allele |
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stabilizing natural selection |
maintains the status quo and acts against extremes |
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single-nucleotide polymorphism (SNP) |
site in the genome where there is a base-pair difference among chromosomes that is common enough to be present in 1% of the population |
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negative control |
no response is expected |
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positive control |
a known response is expected |