Utilisateur
Selection occurs within a population but evolution requires generations.
show evolution over long time frames
artifical selection
yes
1. variation is pre existing and can be passed on to offspring
2. selection is based on environment
3. not all offspring survive (those who survive is non random)
4. differential reproduction (those with advantageous traits in that space and time are more likely to survive and reproduce)
didn't propose a theory for inheritance, the concept of mutation was not developed until 1900's
transformational evolution
variational evolution
fossils
an environment where they can fossilize
george cuvier first started studying fossils and first proposed extinctions
it is incomplete, we've only found the easiest to find fossils, hot humid areas rarely have fossils. fossils are also biased because hard and bony parts/ aquatic organisms fossilize better.
due to changing sediment conditons, if the environment that the fossil was in changes it can obscure the date
universe- 13.77 byo and earth- 4.5 byo
because of 4.4 byo meteorite in australia and zircon crystals that are also this old, darwin also hypothesized this because of geological formations in england
at a measurable rate
at dawn of solar system
that our solar system is ancient
approx 3.8byo, esitmated by principle of superpostion
520 Mya: fossils of oldest known chordates (incl vertebrates)
480 Mya: the oldest trackways
475 Mya: oldest land plant fossils
360 Mya: oldest land vertebrates
230 Mya: dinosaurs
180 Mya: Our common mammalian ancestor
150 Mya: birds
no just zircons and stromatolites
deep sea vents and hot springs
that there was tons of energy, carbon and lots of redox worthy chemicals
that there was tons of energy and nutrients, lots of oxidized minerals
where they tried to recreate the conditons of early earth but failed
very little oxygen, lots off ammonia, lots of methane, lots of volcanic activity. These conditions together could cause abiotic synthesis of organic molecules
1.8bya because of acritarchs
used to think 1.6 byo, interpreted as filamentous algae
sponges
known as the ediacaran fauna
segmentation, 3 axis's, more complexity. (ex. trilobite, mollsucs, and first chordates)
Increased O2, allowed more primary productivity, allows emergence of predators, allows inc in body size BUT oxygen levels didn’t necessarily change around Cambrian and larger animals already existed
Evolutionary innovation, evolution of novel traits (ex. Segmentation) allowed increased adaptability (ex. Hox gene cluster evolution may have sparked Cambrian)
Predation and arms race, if predation arose during Cambrian it could explain, inc body size, hard body size, motility/ swimming ability
the late Ordovician and early Silurian period (450 Mya). Most likely liverwort like organisms, possibly co invaded by fungi, vascular plants evolved after
millipede
amniotes produce shelled eggs
this was the paleogene mass extinction event which caused the loss of big reptiles but the little mammals thrived (prob due to loss of predators)
Darwin thought, more shared features= more recent common ancestor
vary with the taxa of interest, have different states, can be morphological, behavioural, biochemical, genetic.
to reconstruct evolutionary relationships so that trees can reflect shared ancestry
life, domain, kingdom, phylum, class, order, family, genus, species
mendel determined that traits of offsprings were determined by parental factors that remained discrete.
traits that have no blending
hand pollinated pea plants with known traits, he was the first to use math to explain predicted traits in offspring
Crossed round and wrinkled peas, all progeny were round (F1)- all showed only one parental phenotype, no blend, these were heterozygote (het) and showed the dominant traits. Then he crossed Rr and Rr and got progeny that were 3 R: 1 W (approximately).
that traits came in pairs and the genes are halved in germ cells
law of dominance, law of segregation, law of independent assortment
most traits dont follow the phenotypic ratios of mendelian inheritance because of multiple alleles of one gene, influence on other genes and influence of environment
a diploid (2n) will only carry 2 alleles in an individual but multiple alleles can exist in population which can create variation in a population without necessarily being influenced by other genes or the environment
ex. pavilion dardanus butterlfies which have multiple alleles which give rise to multiple wing patterns within the same speices
ex. human ABO blood type has 3 alleles, 9 possible genotype within pop, 4 possible phenotypes
most traits are continous
where their phenotypic variation exists on spectrum
polygenic inheritance, where many genes contribute to the same traits
environmental conditions can have a great impact on phenotype, even greater than genotype sometimes.
These conditions can include, temp, availability of nutrients, presence of toxins/mutagen, some can be the maternal effect
Easiest way is to force mate individuals with opposite phenotypes if the progeny will follow a Mendelian inheritance pattern in the F2 but most traits aren’t Mendelian.
it is arranged into chromosomes, multiple linear chrosomes. DNA in eurkaryotes is organzied using histone proteins. The DNA wraps around a histone octomer creating a nucleosome.
The organization of DNA protects it from damage, organizes the nucleus and limits access of transcriptional machinery to DNA
chromsomes are stored in the eukaryotic nucleus (membrane bound organelle), chromosome sizes can vary greatly- msot eukaryotes are diploid (2n)
in the soma of humans cells are diploid but germ cerlls are haploid
DNA to RNA (transcription), RNA to protein (translation). Only one strand of DNA is used as a template.
Translation is carried out by ribosome and uses a universal codon table. 3 nucleotides= 1 amino acid
Redundancy in the genetic code allows mutational tolerance (more than one codon encoding same amino acid. Most of redundancy is @ 3rd codon.)
In most euk, each cell contains the exact same entire genome. Only a fraction of genes are expressed giving rise to different cell types.
Most gene regulation occurs at the level of transcription initiation. This is regulated by a region of the DNA called the promoter.
alternative splicing
Most of eukaryotic genome is not expressed and most doesn’t become protein
genes that have mutated such that they no longer contain a promoter, hence not being transcribed to mrna
markers are specific sequences of DNA, often located throughout the genome, can be used as refrerence points to track the inheritance of genes linked to certain traits. the goal is to find genetic markers significantly associated with the extremes of the trait
jumping genes, products of ancient viral infection. Can change positions within the DNA, can cause mutations by disrupting the genes or regulatory regions that they jump to.
no gemone size is unrelated to complexity, genome size caries greatly between organisms. ex. sea anemones have more genes than humans.
from alternative splicing not from gene #
process by which a single gene can produce multiple different versions of protein, occurs during RNA processing. alternative splicing allows for the exons (coding regions) to be arrange in different combinations leading to the production of multiple proteins from the same gene.
meiosis
4 genetically different haploid gametes
crossing over, independent assortment, random fertilization
pair of chromsomes have same gene order but potentially different alleles
it generate genetic variation and haploid gametes.
due to the crossing over in prophase I (homo chromo exchange genetic material)
and
independent assortment in metaphase I (homo chromo pairs line up, arrange randomly)
and
random fertilization (random sperm and random egg)
only the environment determines if a mutation is harmful (most common), neutral, beneficial (rare).
they rely on very rare benefical mutations for variation
silent muation, missense mutation, nonsense mutation, frameshift mutation
change in a single base pair of DNA sometimes due to DNA replication error or exposure to mutagens
change in DNA seq that doesnt change protein seq
ex. GAA changed to GAG but both of these code for the same amino acid
a change in a single base pair that results in a codon coding for a different amino acid which can affect protein function
ex. GAG mutated to GTG code for a different amino acid which can affect the protein.
point mutation that changes codon to a stop codon, causing protein to be prematurely shortened. Can cause to loos of function or non fuctional proteins.
ex. CAA muated to UAA (stop codon), causes translation to stop early.
deletetion/insertion of nucleotide so that the reading frame shifts of the genetic sequence.this leads to a complelety different protein sequence after the point of mutation which can be devastating to protein function
missense maybe, nonsense, frameshift
no they are common, but the rarer events have greater effects
yes, gain/loss of chromosome
gain or loss of chromosomes, often have great effects
yes
around 61
HW allows us to predict the particular phenotypes in offspring for an entire pop
HW eqbrm provides a null hypothesis for testing evidence of evolutionary change.
if there was no selection/mutation/drift
no, to be satisifed a population must be infinitely large, have no net muation, no net migration, mate randomly, and have no selection (no disadvantageous/advantageous traits)
alleles and genotype freq in offspring would be the same as parent gen
P^2 + 2pq + q^2= 1
p= dominant allele
q= recessive allele