why do diploid cells have 2 copies of each autosomal geen
Diploid cells receive one set of chromosomes from each parent. 1 mark
These sets pair up to form homologous chromosomes. 1 mark
Each homologous chromosome pair therefore carries two copies of each autosomal gene (one from each parent)
monohybrid cross
2 individuals for a single trait
Outline an example of phenotypic plasticity in an animal
When the temperature is cooler, the adult butterflies take on the form “dry season” and live longer, only breeding at the end of the season and have a wing pattern that lookes like dry foliage.
When it is hotter, the butterfly looks like “wet season”, have a shorter life span but breed more during it, they also get a distinctive eye spot wing pattern to avoid predators.
phenotypic plasticity
Ability of an organism to exhibit variations in its physical characteristics or traits in response to environmental influences
What causes PKU
Mutation in a gene on chromosome 12.
what cant happen with PKU
It codes for enzyme used in metabolism called phenylalanine hydroxylase (PAH) that converts the amino acid phenylalanine (Phe) into tyrosine (Tyr).
the symptoms of PKU?
Phe not broken down: toxic levels build up,
musty odour from skin and urine,
fair skin,
eczema,
seizures,
hyperactivity.
brain damage eventually.
How can we identify if an individual has PKU?
Testing at 1-2 days old with a heel prick that gets a drop of blood to test on filter paper for the Phe:Try ratio. If high Phe, following up tests will happen.
How is PKU treated?
Dietary plan to keep protein levels low and frequent blood tests.
What is a SNP?
A single nucleotide in DNA gets randomly changed for another (mutation).
all dipliod cells contain
2 copies of each autosomal gene
pku is an example of
Phenotype impacted envromental factors
treat wth a low-phe diet
Phenotypic plasticity is
the capacity to develop traits suited to the environment experienced by
an organism, by varying patterns of gene expression
what is pku
Phenylketonuria (PKU) is a recessive genetic condition caused by mutation in an autosomal gene that
codes for the enzyme needed to convert phenylalanine to tyrosine.
phenotype for codominance
dual phenotype
blood groups
phenotype for incomplete dominance
intermediate phenotype
Explain the reason that Morgan’s results did not agree with expected Mendelian ratios in a dihybrid cross.
Mentioned recombinants (new combination of alleles from parents), which relates to crossing over and changes in expected ratios
if genes are on the same chromosome/linked they wont be independentaly assorted
recombiants are rare cause crossing over between close genes doesnt happen much
The molecular basis of inheritance is how
DNA stores genetic information, replicates, and is passed from parents to offspring, determining inherited traits.
PAtterns of inheritance in animals + plants
can be men…..
Mendelian types like autosomal dominant, autosomal recessive, X-linked dominant, and X-linked recessive inheritance.
Non-Mendelian patterns, such as incomplete dominance or codominance
what happens from genes segregating and assoriting randomly in meiosis
random allele combinations for the resulting gametes
frequency of unlinked genes vs linked crossing over
50% for unlinked
basically none for linked as they are close on the chromosome