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constituitive proteins
always active (require most amount of energy)
proteins made in inactive state
can be activated in presence of an enzyme
translational control (prokaryotic)
some genes are transcribed and not translated
transcriptional control (prokaryotic)
some genes are never transcribed (least energy required)
negative control
regulatory protein is a repressor
positive control
regulatory protein is an activator
inducible operon
normally off, must be turned on (catabolic)
repressible
normally on, must be turned on (anabolic)
catabolic
breakdown
anabolic
synthesis
repressor
binds to operator to stop transcription
inducer
binds to repressor to change its shape so it can no longer bind with operator (inducible)
corepressor
activates repressor so it can bind to operator and stop transcription (repressible)
activator (prokaryotic)
binds to activator binding site to cause transcription
substrate
binds to activator to activate it and cause transcription (inducible)
product
binds to activator to change it’s shape so it can no longer bind to activator binding site (repressible)
lac operon
negative control, inducible
repressor: lac repressor
inducer: alolactose
trp operon
negative control, repressible
repressor: trp repressor
corepressor: tryptophan
Catabolite activator protein (CAP)
binding upstream of promoter results in stronger binding of RNA polymerase to DNA template and maximum transcription
cyclic AMP activates CAP protein
low glucose —> more cyclic AMP —> more activated CAP —> maximum transcription
transcriptional regulation (eukaryotic)
determines when genes are transcribed (chromatin, DNA)
post-transcriptional regulation
determines types and availability of mRNAs to ribosome (pre-mRNA, mature mRNA)
translational regulation
determines rate at which proteins are made (initiation of protein synthesis)
post-translational regulation
determines availability of finished proteins (new polypeptide chains, finished proteins, protein breakdown)
histone acetyltransferase
acetylation by HA breaks interaction between DNA and histone tails
histone deacetylase
deacetylation by HD causes acetyl groups detach so tails bind to DNA
regulation by activators
enhancer contains enhancer regulatory sequences
activators bind to enhancer regulatory sequences
coactivators bind to activators at enhancer and to proteins at proximal region creating a loop which leads to maximum transcription
steroid hormone regulation of gene expression
steroid hormone binds to previously inactive steroid hormone receptor, activating it
complex moves into nucleus
complex attaches to steroid hormone response element, causing maximum transcription with no regulation
microRNAs/RNA interference
microRNAs form hairpin loops
loop is transported out of nucleus into cytoplasm
dicer protein removes end of loop (lariat) leaving dicer + dsRNA
protein complex attaches
protein complex degrades one strand of dsRNA creating the miRNA induced silencing complex
miRISC binds with mRNA that has complimentary sequences (imperfect pairing)
mRNA cannot be translated because RNA is unstable
mRNA bound with miRISC preserves it for longer
short interfering RNAs
viral origin
microRNAs form hairpin loops
loop is transported out of nucleus into cytoplasm
dicer protein removes end of loop (lariat) leaving dicer + dsRNA
protein complex attaches
protein complex degrades one strand of dsRNA creating the miRNA induced silencing complex
binding with miRISC results in perfect pairing and mRNA is destroyed
transcription specificity in eukaryotes
activators are unique to genes, so presence of specific activators and enhancers determine which genes are transcibed
expression of activators is in some response to external stimuli
activators (eukaryotes)
position RNApol
release RNApol from promoter
accelerate binding and assembly of general transcription factors
activating coactivators
repressors (eukaryotes)
mask activation site
interfere with general transcription factors
remodel chromatin
particulate theory of inheritance
Mendel - characteristics are passed on to offspring in discrete hereditary factors (genes)
principle of segregation
Mendel - two alleles of a gene segregate from each other during gamete formation
reciprocal cross
reversing sex of parents for a given trait to test if it is sex-linked
test cross
crossing individual with unknown phenotype and individual with known phenotype (often recessive)
selfing
crossing between 2 individuals from same generation
backcross
crossing one offspring with parent
incomplete dominance
heterozygous individuals have intermediate phenotype, related to gene expression
codominance
both alleles are expressed in heterozygous individuals
multiple alleles
gene has more than 2 alleles that exist in the population
epistasis
effect of one gene masks expression of another gene
recessive: 2 recessive alleles mask expression of second gene
dominant: one dominant allele masks expression of second gene
polygenic inheritance
a trait is controlled by multiple genes
pleiotrophy
one gene having multiple cascading effects
Thomas Hunt Morgan
established autosomal linkage and sex linkage
recombination frequency
(total # recombinants/total offspring) x 100 = rf
deletion
segment lost from a chromosome
duplication
segment is broken from one chromosome and inserted into its homolog, adding to the ones already there
translocation
segment is attached to a different, nonhomologous chromosome
inversion
segment reattaches to same chromosome, but in reversed orientation - order of genes is reverses
Implications of Hardy Weinberg law
Reproduction alone does not change allele frequencies
Allele frequencies can be used to determine genotypic frequencies only if population is in HW equilibrium
A single generation of random mating produces equilibrium genotypic frequencies
If a population is not in HW equilibrium, one of the assumptions has been violated.
Conditions necessary for HW to be in effect
no mutation
no migration
large population
all organisms are equally fit
random mating
Measures of population variation
variance in allele frequency
observed heterozygosity
Forces of microevolution
mutation
gene flow
genetic drift
natural selection
nonrandom mating
Mutations
increases variability
Gene flow
movement of genes into and out of a population
migration increases variation within new population and decreases variation within original population
homogenizes gene pool between populations
genetic drift
fluctuations in frequency of alleles in a population
small populations are more prone to drastic changes in gene pool than large populations
genetic bottleneck and founder effect
genetic bottleneck
large gene pool in original population, but gene pool in surviving population is more restricted
founder effect
small number of individuals migrate out of a population to start a new population
nonrandom mating
selecting mate with particular phenotype and underlying genotype
inbreeding
inbreeding
genetically related individuals mate with each other
increases frequency of homozygous phenotypes and decreases frequency of heterozygotes, so recessive phenotypes are often expressed
morphological species concept
individuals of a species share measurable physical traits that distinguish them from individuals of other species
pros: applies for sexual and asexual species, applies for fossils
cons: members of same species can look very different, convergent evolution
biological species concept
reproductive isolation: organisms are separate species if they’re unable to reproduce viable offspring
pros: very applicable to real world situations
cons: hybrids
phylogenetic species concept
cluster of populations that emerges from same small branch (evolutionary relationships)
pros: applicable to all organisms
cons: over classification
ecological species concept
based on where and how organisms live
pros: works for all types of organisms
cons: unclear definitions of ecological niches, convergent evolution
subspecies
members or a species exhibit dramatic, easily recognized phenotypic variation
ring species
plant and animal species with ring shaped geographical distribution surrounding uninhabitable terrain
clinal variation
species distributed over a large, environmental diverse area may exhibit a pattern of smooth variation in traits along a geographical gradient
allopatric speciation
physical splitting of a population
adaptive radiation
rapid speciation from a single ancestor
secondary contact
3 options:
species remain separate and distinct
hybrid zones
interbreeding merging back into single species
sympatric speciation
reproductive isolation evolves between distinct subgroups that arise within one population
autopolyploidy
single species
through error in meiosis, doubling of chromosomes produces diploid gametes, and fertilization of one diploid gamete by another produces a tetraploid zygote
tetraploids are reproductively isolated from diploid population
allopolploidy
2 closely related species hybridize and form polyploid offspring, hybrid offspring are sterile if chromosomes of the two parent species do not pair properly during meiosis
prezygotic isolation
operates before production of fertilized egg, preventing egg and sperm from coming together
ecological isolation
living in different habitats in same region
temporal isolation
reproduction takes place at different times of year, so change of exchanging genes is very low
behavioral isolation
signals of one species are not recognized by another
mechanical isolation
differences in structure of reproductive organs or other body parts physically prevent mating
gametic isolation
species have nonmatching receptors on gametes
postzygotic isolating mechanisms
operates after zygote formation, reducing fitness of hybrids
hybrid inviability
offspring don’t survive
hybrid sterility
offspring are viable but sterile
hybrid breakdown
offpsring have reduced survival and reproduction