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89 Cards in this Set

  • Front
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Which of the following is the most correct explanation of why more antibiotics become ineffective in the treatment of bacterial infection?
Mutations on bacterial genes that cause bacteria’s resistance to drug become positively selected.
Which of the following does not support the hypothesis that teosinte is the progenitor of maize?
More sequence polymorphism is observed in maize population than teosinte population.
Which of the following correctly describes a selective sweep caused by a recent positive selection?
Immediately after the fixation of an advantageous mutation, the amount of genetic variation around the mutation is greatly reduced.
about when did chimpanzees and humans diverge?
5-7mya
“hominin” =
hominids (human-like species in the past) that are sister group of the chimpanzees
Homo erectus
appeared ~1.6 Mya
before 1 Mya, spread from Africa into Asia (to China and Java)
Archaic Homo sapiens
appeared ~300 Kya in Africa, Asia and Europe
differs from “anatomically modern sapiens” in minor respects
best-known population: Neanderthals (Homo neanderthalensis?)
Modern sapiens
appeared ~170 Kya in Africa
Anatomically indistinguishable from today’s humans
overlapped with Neanderthals but abruptly replaced them (in Europe about 40,000 years ago)
when did the first mitochondrial dna appear? (according to records)
~140,000 years ago  “mitochondrial Eve”
Why phylogenetic trees?
Helps conceptually distinguish between evolution (pattern) and mechanisms of evolution (process)
Provides an organizational tool for thinking about biodiversity and evolution
What do Phylogeny, Evolutionary tree, Cladogram, Dendrogram, Phylogram all have in common?
They are all alternative Phylogenetic tree names
taxon/ taxa
the ends of the trees- species/ genes
nodes
the splitting points on the trees- extinct common ancestors
root
the node at the end of the tree- the common ancestor of all taxa
internal branch
node to node
external branch
node to tip
bifurcating tree
each branch leads to a pair of species
polytomy
more than two branches leading from a node
branch numbers
Indicate level of support or confidence
Bootstrap percentage
Ranges from 100 (high confidence/support) to 0 (no confidence/support).
Monophyletic Group
Single origin
The given set of taxa forms a group that contains
their most recent common ancestor and all its
descendants
Paraphyletic Group
– Single origin, but with exceptions
– The given set of taxa forms a group whose
founding ancestor produced some descendants
that are not in the group
Polyphyletic Group
– Multiple independent origins.
– The given set of taxa forms multiple groups each
of which is either monophyletic or paraphyletic
Homology
characters which are
similar due to common descent
– They are inherited from a common
ancestor
Ex: 8 Vertebrate in mammalian necks
Analogy:
characters which are similar
due to convergence or parallel
evolution
Ex: bird and bat wings
– They are NOT inherited from a common
ancestor
So which tree most likely represents the evolutionary history?
the most parsimonious
evolutionary distance
the number of substitutions that have occurred in two sequences since their divergence from a common ancestor
How can you transform p distance (which tapers off) into true distance?
Jukes Cantor distance
Assumptions of Jukes Cantor
Each nucleotide (A, C, G, & T) occurs with
equal frequency (i.e., 25% each)
– All sites in a sequence have the same
mutation rate
– The rate of all types of substitution are
identical (e.g., A → C = A → G = A → T)
– Reversibility: C → G = G → C
How to correct p distance into true distance?
Poisson Distance
Max protien p-distance?
Max nucleotide distance?
0.95 (1/20)
0.75 (3/4)
how to calculate p distance
#of differences/#of common sites (meaning total sites)
Lets say there are 7 nucleotide differences between sequences of DNA from a cow and a human- what would that tell you?
Each branch accumulated 3.5 nucleotide differences for a total of 7
UPGMA method
“Unweighted Pair-Group Method with Arithmetic mean”
UPGMA assumes constant rate
average rate r=distance/2t
quantitative traits
phenotypes that show continuous variation rather than simple Mendelian descrete variation the most phenotype variation we observe
Fitness=viability x fertility
quantitative trait
early investigator of evolution
believed that characteristics from both parents blended together to make offspring
Did not accept Mendel's theory, particulate inheritance cannot explain phenotypic variation
P=Xm + Xp + E
The phenotype value
Xm
mating is done at random
Xp
Phenotypic variance
E
environmental variance
Xmi or Xpi
is what determines the allele or alleles this individual receives from the corresponding parent
All Xmi and Xpi are equal when
there is no genetic variation in the population the variances become zero
Va
variance of genetic variation
Ve
variation due to environmental variation
Va>0
individuals in the population carry different sets of alleles that produce different phenotypes

Va increases with genetic variation (polymorphism) in the population
polymorphism
when multiple alleles of a gene within a population express different phenotypes
additive genetic variation
Genetic variance associated with the average effects of substituting one allele for another
polygenic variation
having different sources of an orgin

ex: pigmentation in mice on the beach and mainland of Florida are different variations of fur coat color brown, white, dark, etc.
what happens if phenotypic effects of alleles are not additive?
non-additive effects increase phenotypic variance beyond Va
h2=Va/Vp
Narrow sense heritability
H2=Vg/Vp
Broad sense heritability
heritability
proportion of phenotypic variance that can be explained by genetic variation

determines the correlation between relatives

determine the response to directional selection on phenotype
h2
is equal to the slope of regression of offspring values on mean of two parents
h2=1---> Vp=Va
phenotype differences are entirely due to genetic differences
h2=0 --> Va=0
phenotype difference are entirely due to environmental differences
corr {Pa, Pb} = r2
correlation of phenotypic values in pairs of individuals A and B
R is
the coefficient of relationship: the probability that one allele chosen from individual A is found in individual B (proportion of shared alleles)
phenotypic variance and heritability depends on...
allele frequency
Charles Darwin and finches
noticed a great diversity of bill morphology in closely related finches--rapid evolution upon colonization

ex: Peter Grants surveyed during drought on finches. Drought lead to shortage of small soft seeds selection for finches with large beaks. Birds with large beaks are expressed more in pop.
Genetic variation in a quantitative trait is
raw material for natural selection
what maintains genetic variation in a quantitative trait
New mutations
Variable selection
Intra-species competition
New mutation
new mutations compensate for loss of variation due to selection
variable selection
optimum phenotype change in space and time
Intra-species competition
avoidance of competition may promote genetic diversity
Pleiotrophy
one genetic change affects multiple phenotypes

mutation for smaller size may produce low fertility

environmental change may favor to increase both size and fertility
An extreme directional change in one phenotype
is accompanied by fitness-lowering changes in other phenotypes
P element
an element that replicates by inserting its copy at random positions in genome
what's in a good "species" definition
classify organisms systematically, discrete groups, clusters, products of evolution, variety of organisms
biological species concept
reproductive isolation genetic differences between population prevents the exchange of genes- no mating

Problems: restricted to sexual outcrossing organisms. Reproductive isolation cannot be known. borderline cases. hybrid zone.
hybrid zone
practice mating with other individuals- inbreeding- speciation
outcrossing
practice mating with other individuals- inbreeding
phylogenetic species concept
luster of organisms different from other groups where there is a parental pattern of ancestry

applies to asexual organisms
may lead too many species, occur whenever a population undergoes fixation of genetic differences in related pop.
gaining acceptance among systematics
genealogical species concept
species are exclusive groups of organisms which one or more are closely related to one another than outside the group
recognition species concept
a species is the most inclusive population of individual biparental organisms that share common fertilization system
Cohesion species concept
a species is the most inclusive having potential for phenotypic cohesion through intistic cohesion mechanism
zygote
a single celled individual formed by union of gametes
prezygotic isolation
premating barriers ecological isolation- breeding at different seasons, diff. habitat

incompatibility of sperm and egg
In a simple model of infectious disease, the number of new infections produced by an infected host is given by R0. Which of the following factor is positively correlated to R0?
number of uninfected hosts
Which of the following is an important reason that vector-borne diseases are generally more lethal than directly transmitted diseases?
Pathogens transmitted directly are under evolutionary pressure not to decrease the host’s mobility
Loss of function in a gene
Degeneration
pseudogene
Neofunctionalization
One copy acquires adaptive mutations and gains a new function. The other copy maintains the original function
Subfunctionalization
Two copies lose partial functions complementarily
- Ex) Original gene was expressed in both brain and liver. One duplicate copy loses expression in brain. The other copy loses expression in liver.
Which fates of the new duplicates result in new genes?
subfunctionalization and neofunctionalization
Have diverged from a common ancestral gene by phylogenetic splitting
Orthologous genes
paralogous genes
evolve parallel (think of orthologous as perpendicular)
Trans-acting factors
Different cell types express different sets of genes (by tissue/cell-specific trans-acting factors)
diffusible regulatory proteins (transcription factors produced by other genes) that bind to DNA and switch transcription on and off.
Cis-acting factors:
segments of DNA that do not encode proteins, but interact with trans-acting factors to regulate the expression of nearby genes. Usually located at 5’ upstream of protein-coding sequence