Topic 3.4 Modes of Inheritance Flashcards
Principles of inheritance
Gregor Mendel established the principles of inheritance via experiments (he crosses large number of pea plants). His findings pioneered current scientific understandings:
- Organisms have heritable factors (genes)
- Parents contribute equally to inheritance by supplying one version of the gene each (alleles)
- Gametes contain only one allele of each gene (haploid)
- Fusion of gametes results in zygotes with two alleles of each gene (diploid)
It is now known that the separation of the two alleles of each gene into separate haploid gametes occurs via. meiosis.
Genotype
A genotype is the allele combinations for a specific trait
There Are three possible types of allele combinations
- Homozygous: Both alleles are the same (e.g. AA)
- Heterozygous: Alleles are different (e.g. Aa)
- Homozygous: Only one allele (e.g. X/Y genes in males)
Phenotype
A phenotype is the physical expression of a specific trait
- It is determines by genotype and environmental factor
Modes of inheritance Complete Dominance
Complete Dominance is when one allele is expressed over another.
- Dominant allele is expresses in heterozygote (capital letter)
- Recessive allele is masked in heterozygote (lowercase letter)
A recessive phenotype can only be expressed in homozygotes.
- Heterozygote will display the dominant phenotype
Modes of inheritance: Codominance
Both alleles are equally expressed in the phenotype.
- Heterozygotes have distinct phenotype (superscript letter)
- An example of co-dominance is the ABO blood system
Genetic Diseases
genetic Disease can be due to recessive, dominant or co-dominant alleles
- Recessive conditions are most common as heterozygotes are carriers.
Genetic Disease: Autosomal Recessive
- Cystic fibrosis is caused by mutated CFTR gene (chromosome 7)
- Produces thick muscus that clogs airways and causes respiratory issues
Genetic Diseases: Autosomal Dominant
- Huntington’s disease us causes by a mutated HTT gene (chromosome 4)
- An amplification of CAG repeats (>40) leads to neuro-degeneration.
Genetic Diseases: Autosomal Co-dominant
- Sickle cell anemia is caused by mutated HBB gene (chromosome 11)
- Sickling of blood cells leads to anemia and other complications
Radiation Exposure
Radiation and mutagenic chemicals increase mutation rates and can cause genetic diseases.
- most genetic diseases is humans are rare.
Radiation Exposure examples
- Nuclear bombing of Hiroshima (1945)
- Accident / meltdown in Chernobyl (1986)
Radiation exposure Long-Term consequences
- In increase incidence of caner
- Reduced immunity (↓ T cell count)
- Congenital abnormalities (Chernobyl only)
- A variety of organ-specific health effects (e.g. liver cirrhosis, cataract induction, etc)