Splicing = removal of introns from pre-mRNA to form mRNA
introns prevent polypeptide from forming
happens in nucleus & mRNA leaves via nuclear pores after
splicing only happens in eukaryotes
prokaryotes don't have introns so mRNA is immediately formed
Protein synthesis: Translation = forming of polypeptide chain using mRNA base sequence and tRNA
mRNA leaves nucleus & attaches to a ribosome from the start codon
tRNA with complementary anticodon attaches to start codon
tRNA has specific amino acid attached to it & held is place by ribosome
Ribosome moves along mRNA to attach to 2 amino acids on tRNA by peptide bond
catalysed by enzyme & ATP
Continues until ribosome reaches stop codon on mRNA & ribosome detaches
polypeptide enters golgi body for folding & modification
Meiosis = cell division forming 4geneticallydifferent daughter cells with half the amount of DNA as the parentcell
haploid cells produced
to maintain constantno. of chromosomes in adult of species
occurs in sex organs
Genetic diversity: Crossing Over
prophase 1 - homologous pair of chromosomes formed
chromatids from each pair crossover & twist around each other
twisting causes portion of chromatids to breakoff
broken portions rejoin with chromatids of its homologous pair
Genetic diversity: independent segregation
when homologous pair of chromosomes line up in metaphase - random line up of homologous pairs
2^n = total no. of possible chromosome combinations
n = number ofchromosomes
Meiosis I
Prophase I:
chromatic condense and coils
homologous pairs form
bivalents = homologous pairs of chromosomes
Metaphase I:
bivalents line up along equator
Anaphase I:
homologous pairs pulled by spindle fibres to poles of cell
independent segregation occuring
Telophase I:
chromosomes reach poles & often go straight into meiosis II
spindle breaks down & nuclear envelope reforms
Meiosis II
Prophase II:
spindle forms at right angle to original spindle
nuclear envelope breaks down if reformed
Metaphase II:
chromosomes line up at equator of the cells with spindle attached to centromere
Anaphase II:
spindle fibres shorten causing centromere to divide & chromatids to seperate
Telophase II:
chromosomes reach poles & uncondense
nuclear envelope reforms & spindle breaks down
4 haploid cells formed
Mutation = random change in the sequence of bases in agene
gene mutation = changes to 1 or more nucleotides or a change in the DNA base sequence
silent mutation = gene mutation that doesn't affect the amino acid coded for
due to DNA being degenerate
mis-sense mutation = gene mutation that changes the amino acid coded for
substitution mutation = type of genemutation where a nucleotidereplaced with another nucleotide with a differentbase
may code for a differentaminoacid & affect bonds formed tertiary structure of protein -> can't function
nonsense mutation = type of substitutionmutation where a premature'stop'codon coded for
deletion = type of genemutation where a nucleotide is lost from DNAsequence
has a 'knock-on' effect called a frameshift & changes way DNA is read
insertion = type of genemutation where a nucleotide is added to DNAsequence
also causes a frameshift
chromosomal mutations = changes to the structure or number of whole chromosomes
polyploidyl = condition caused by a change in whole sets of chromosomes
occurs when organisms have 3 or more sets of chromosomes instead of 2 but mainly occurs in plants (humans wouldn't develop)
non-disjunction = condition caused by changes in the number of individualchromosomes
when individual homologous pairs of chromosomes fail to seperate in meiosis
leads to having 1 more or 1 less chromosome
thus allcells of adult of species have 1 more or less chromosome
Required practical 6: effect of antimicrobial substances on microbial growth
method:
spray bench with disinfectant & wipe down with paper towels
place bunsen burner on heatproof mat & light it
name & date the underside of the agar plate
wash your hands
genetic diversity = total number of different alleles in a population
population = a group of individuals of the same species that live in the same place and can interbreed
greater no. of differentalleles in a species -> greater genetic diversity of that species
types of genetic adaptation:
structural adaptation - e.g. fur colour
physiological adaptation - e.g. levels of fat stored
behavioural adaptation - e.g. using rocks to get food
reduction in genetic diversity
genetic bottleneck = population is greatly reduced in size by an extremeevent, limiting the genetic diversity of the species
smaller gene pool -> less genetic variation
founder effect = smallnumber of organisms form a newpopulation and only have a few different alleles from the initialgenepool
completely changes frequency of alleles in new colony compared to larger parent colony
may lead to more genetic disease
natural selection = process in nature causing individuals with advantageous traits to be more likely to survive & reproduce & pass on those traits to their offspring
genetic diversity is the enabling factor of natural selection
only certain individuals are reproductively successful -> affects allele frequency in a population
A) random mutation occurs & causes genetic diversity
B) new allele may now by advantageous to the possessor
C) individuals more likely to survive thus reproduce
D) greater proportion of next gen. inherits adv. allele
E) over gens. allele frequency increases in population
selection pressure = an evolutionary force causing particularphenotype to be more favourable in a certain environmental conditions
polygenes = multiple genes that influence a characteristic
more likely to be influenced by the environment
directional selection = the environment favours individuals with alleles for charactersitics of an extreme type
mean changes
stabilising change = the environment favours individuals with alleles for characteristics closer to a specific value
mean stays the same but the standard deviation decreases over time
A) directional selection
B) stabilising selection
classification = groupingoforganisms
artificial classification = groups organisms based on differencesuseful at the time
called analogous characteristics = characteristics with samefunction but differentorigins
phylogenetic classification = hierarchy where groups contained within largercompositegroups & have nooverlap
no overlap -> every item fits in 1species
based on phylogenetic trees between organisms & ancestors' shared characteristics
homologous characteristics = characteristics with similarevolutionaryoriginsregardless of function in adult of species
phylogeny = evolutionary relationships between organisms
phylogeny of an organism reflects the evolutionarybranch that led to it (modeled by phylogenetic trees)
taxonomy = theory & practice of biological classification
taxon = groups within a phylogenetic biological classification
taxonomic rank = position of agroupintheheirarchy
3 domains by Carl Woese
Archaea = single-celled prokaryotes with some eukaryotic features
protein synthesis more like eukaryotes
no murein in cell walls -> fatty acids bonded via ether linkages
1 kingdom: archaebacteria
bacteria = single-celled prokaryotes
has 7OS ribosomes (smaller than eukaryotic ones)
1 kingdom: eubacteria
eukarya = organisms made of 1 or more eukaryotic cells