Genetic Variation Simplified Revision Notes for A-Level AQA Biology
Revision notes with simplified explanations to understand Genetic Variation quickly and effectively.
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7.3.1 Genetic Variation
infoNote
Genetic variation refers to differences in the alleles of genes between members of the same species. It arises from a combination of genetic and environmental factors.
Sources of Genetic Variation
Random Fertilisation:
During sexual reproduction, gametes (sperm and egg) with different alleles combine randomly, producing offspring with unique combinations of alleles.
Meiosis:
Independent assortment of homologous chromosomes during meiosis means alleles are distributed randomly into gametes.
Crossing over between homologous chromosomes creates new combinations of alleles.
Mutation:
Changes in the DNA sequence of a gene can lead to the formation of new alleles.
These mutations can be inherited if they occur in gametes, contributing to genetic variation in the next generation.
Environmental Influences on Phenotypic Variation
Phenotype is determined by both genetic makeup and environmental conditions.
Example: Two plants with the same alleles for flower colour may display different colours if one grows in mineral-deficient soil, preventing pigment production.
Normal Distribution in Traits
When environmental factors influence a polygenic trait (controlled by multiple genes), the variation often follows a normal distribution.
Example: Adult height in humans. Most individuals are close to the mean height, with fewer individuals at the extremes (very short or very tall).
Environmental factors influence phenotypes, causing variation even in individuals with identical genotypes.
Recognise examples of traits influenced by both genetic and environmental factors.
Understand the role of normal distribution in polygenic traits.
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