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87 Cards in this Set

  • Front
  • Back

most common recent ancestor (MCRA)

share closest connected node

tRNA

carries individual amino acids to ribosomes to make protein

rRNA

helps make up ribosomes

ribosome

organelle in cytoplasm - synthesizes proteins

genetic code

translation of codons to amino acids

phospholipid

derivatives with 2 hydrophobic fatty acids and a hydrophilic phosphate group (makes up bilayers)

carbohydrate

source of energy and structure, made of sugars, C, H, O: 1:2:1

allele

different variations of a gene - from mutations

binary fission

division of prokaryotic cells

centromere

holds together sister chromatids

chiasmata

crossover parts of bivalents with sister chromatids

cytokinesis

division of cell cytoplasm

diploid

2 complete sets of chromosomes (human somatic cells)

haploid

1 complete set of chromosomes (human germ cells)

homologous chromosomes

not sex chromosomes; one from father, one from mother

interphase

part of cell cycle: G1, S, G2; preparation for cell division

M-phase

part of cell cycle, parent cell divides into 2 daughter cells, mitosis and cytokinesis

meiosis

division of sex cells, results in 4 daughter cells, half the chromosomes, daughter cells unique

metaphase

spindle complete, chromosomes line up

mitosis

division of cell nucleus

non-disjunction

failure of chromosomes/chromatids to separate properly during cell division

recombination

rearrangement of genetic material especially crossing over

S-phase

synthesis, replication of DNA between G1 and G2

sister chromatids

duplicated chromosomes connected to parent after S-phase, genetically identical

zygote

2 gametes come together and fuse, result of fertilization

backcross

crossing hybrid with parent of genetically similar to parent

F1/F2

First offspring/F1 offspring


genotype

genetic makeup

hybridization

interbreeding between 2 different varieties of a species or organism

nonsense mutation

creates stop codon

nonsynonymous (missense) mutation

results in amino acid replacement (point mutation)

phenotype

observable characteristics or traits

polymorphism

genetic difference among individuals common so that it is probably in a group of 50 individuals

reciprocal crosses

expression of trait male and female parents interchanged

segregate

formation of gametes - half get one allele and half get other allele

synonymous (silent) mutation

does not change amino acid for codon

testcross

cross of unknown genotype with homozygous recessive genetype

true-breeding

phenotype of each offspring identical to previous

translocation

one part of a chromosome breaks off and attaches to another

codominance

both alleles are dominant

dihybrid cros

cross between 2 pure lines that differ in 2 observed traits

incomplete dominance

phenotype of heterozygous is between the two homozygous genetopes

independent assortment

two different traits are not dependent on each other

mitochondrial inheritance

transmission of mitochondrial inheritance from parent to child

maternal inheritance

traits passed down from mother to child

pedigree

diagram of family genetic history

segregation

during meiosis each gamete receives either maternal or paternal gene

autosome

chromosome that is not a sex chromosome

epistasis

genes that modify the expression of other genes

genetic distance

measure of genetic divergence

linkage

genes transmitted together in inheritance - don't sort independently

linkage mapping

map of genes in terms of recombination frequency

non-recombinant type

allele present in same combination as in the parents

pleiotropy

one gene effects multiple seemingly unrelated pheonotropic traits

reciprocal cross

pair of crosses between male of one strain, female of another strain, and vice versa

recombinant type

result of a crossover

recombination

crossing over of chromosomes

sex-linkage

genes located on the sex chromosome

analogous

similarities due to independent adaptation by different species

ancestral trait

trait shared by a group of organisms as a result of descent from a common ancestor

convergent evolution

independent evolution of similar features in species of different lineages

derived trait

traits existent in a present organism not present in their ancestors

fitness

measure of the extent to which an individual's genotype is represented in the next generation

homologous

characters that are similar because of descent from a common ancestor

monophyletic group

all share an ancestor not shared with any other species

parsimony

choosing the simpler hypothesis for a given set of observations

polytomy

an unresolved pattern of divergence, a node with multiple branches


sister taxa

share a MRCA, more closely related to each other than to any other group

shared derived trait (synapomorphy)

homology shared by some, but not all members of the group

allele frequency

number of alleles present in the population divided by the total number of alleles

allele fixation

all genes contain a particular allele

balancing natural selection

maintain 2 or more alleles in a population, maintain an allele between 0% and 100% (sickle cell)

continuous (polygenic) trait

variation occurs along a spectrum

discrete trait

clear alternative states (yellow/green peas)

directional natural selection

leads to a change in the trait over time, level of variation is the same

disruptive natural selection

in favor of extremes and against intermediates, mean stays the same, variability increases or stays the same

genotype by environmental interactions

phenotype result of interplay of genes and the environment

heritability

proportion of total variation in the trait that is due to genetic differences among individuals

heterozygote advantage

heterozygote fitness higher than either homozygote

polygenic (quantitative) inheritance

when many genes and environment affect a trait

positive selection

increases the frequency of a favorable gene

relative fitness

fitness of a genotype divided by fitness of maximum genotype

negative selection

decreases the frequency of a harmful allele

stabilizing natural selection

maintains the status quo and acts against extremes

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

negative control

no response is expected

positive control

a known response is expected