Inheriting Alleles (DP IB Biology)
Revision Note
Phenotypic Plasticity
Phenotypic plasticity is the idea that although genotype remains fixed throughout an organism's lifetime, the way that the phenotype is expressed can vary during this time
An organism’s internal or external environment can influence gene expression patterns, and therefore phenotype
The levels of regulatory proteins or transcription factors can be affected in response to environmental stimuli such as light, and chemicals including drugs and hormones
For example, enzymes are activated in response to ultraviolet radiation and increase the expression and production of melanin, leading to skin pigmentation
Temperature can also influence gene expression as demonstrated by organisms
The Himalayan rabbit (Oryctolagus cuniculus L.) possesses a gene for the development of pigmentation in its fur
The gene is inactive above 35°C but active between 15°C and 25°C
In the parts of the body that are cooler such as ears, feet and nose the gene becomes active making these areas black
Inheriting Recessive Alleles: Phenylketonuria
Phenylketonuria (PKU) is an inherited condition caused by a recessive allele on an autosome
It is a condition that can lead to symptoms such as mental disorders and seizures
It is caused by a build-up of the amino acid phenylalanine in the body
Phenylalanine comes from broken down protein from diet and our cells
The enzyme phenylalanine hydroxylase breaks down phenylalanine
This enzyme is coded for by the PAH gene
PKU is caused by a mutation to the PAH gene that results in a non-functional enzyme so that the phenylalanine does not get broken down
In the UK around 1 in 10,000 people are born with PKU
In order for a child to have PKU, they must first inherit two recessive alleles from each of their parents
Because it is caused by a recessive allele it means that two non-PKU sufferers could have a child with PKU if both parents are heterozygous carriers of the mutated PAH gene
An example genetic cross is shown below:
A genetic cross between two PKU carrier parents diagram
Diagram showing the parental phenotypes, genotypes, gametes and a Punnett square predicting the possible genotypes of their offspring. Both parents are PKU carriers and their offspring have a 25% chance of inheriting the disorder.
The genetic cross shown on the Punnett square above demonstrates that the offspring of the PKU carrier parents have a 75% chance of not having PKU and a 25% chance of inheriting 2 PKU alleles and therefore having the condition
This pattern of inheritance is the same with any autosomal recessive condition, for example cystic fibrosis
Every baby born in the UK and in many other countries around the world are tested for several genetic conditions including PKU
The babies have a small prick of blood taken from the sole of their foot a few days after being born in order to be screened for the condition
Examiner Tips and Tricks
It should be the case that in most exams letters will be chosen for genetic crosses that have very different upper and lowercase appearances. If you are ever asked to use a letter in an exam that has a similar upper and lowercase appearance, such as P and p, make sure to overly exaggerate the difference to ensure there is no ambiguity during marking.
Single Nucleotide Polymorphisms & Multiple Alleles
Many genes have more than two alleles
However, a diploid individual will still only inherit two of the possible alleles
Alleles differ from each other by one or only a few bases
Even a very small change in base sequence can bring about a large effect in gene function, with a large knock-on effect on the phenotype
Even though different alleles of a gene have slightly different base sequences, they still occupy the same locus on the chromosome
Since the Human Genome Project, sophisticated techniques can analyse different alleles
The exact positions where bases differ between alleles are called SNPs or snips (Single Nucleotide Polymorphisms)
An allele can have several SNPs but still only differ by a few bases from its other allele
Multiple Alleles: ABO Blood Groups
Inheritance of blood group is an example of co-dominance with multiple alleles
This is of critical importance when deciding to give blood transfusions following injury or illness
Use of the wrong blood group can cause an immune response that coagulates (solidifies) blood, leading to clots and serious illness/death
There are three alleles of the gene controlling a person's blood group instead of the usual two
I represents the gene
Superscripts A and B represent the codominant alleles, IA for example
Lowercase i with no superscript represents the recessive allele
IA results in the production of antigen A on the surface of red blood cells
IB results in the production of antigen B on the surface of red blood cells
i results in no antigens being produced on the surface of red blood cells
These three possible alleles can give us the following genotypes and phenotypes
Blood Genotype & Phenotype Table
We can use genetic diagrams to predict the outcome of crosses that involve the codominant alleles controlling blood groups
Worked Example
Show how a parent with blood group A and a parent with blood group B can produce offspring with blood group O.
Punnett square of the inheritance of blood group
Punnett square showing the inheritance of blood group with two heterozygous parents, type A and type B
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