Lecture 6: Genome Complexity Flashcards
How can mutations lead to phenotypic variation?
Can cause changes in gene expression or protein products
How can new genes be made?
From gene duplications and non-coding DNA
Mutations affecting what areas of DNA are likely to have an impact on gene expression?
promotor region, enhancers/silencers
What is beak shape diversity in Darwin’s finches an example of?
Regulatory evolution
What was examined from 6 of Darwin’s finches and what did they find?
expression patterns of growth factor genes in 6 of Darwin’s finches at different development stages. found expression pattern of Bmp4 correlates with beak depth and breadth. More Bmp4 means greater sized beak.
How can the protein products be changed?
AA subs/ deletions/ additions can change the coding frame and truncate the protein.
How can chromosomal rearrangements create new genes?
gene duplications, fusion/fission
Why are mutations in non-coding areas unlikely to be fixed in the population?
Unlikely to be kept as are unlikely to be beneficial in in non-coding region
What is likely after duplication?
For both copies to acquire further mutations
What are the three types of mutation likely to arise after duplication?
Non-functionalisation, subfunctionalisation, neofunctionalisation
What is non-functionalisation?
most of these are lost and degrade in a few million years which is the most common fate
What is subfunctionalisation?
Where both copies only partially fullfill the function of the original gene. is the most common route for maintaining two copies.
How does gene expression evolve?
Through changes on promoter/enhancer/silencer regions, acquisition of novel regulatory elements, mutations or expression changes in activator/repressor machinery, changes in chromatin structure.
What is neofunctionalisation?
one gene gets another function but is very rare.
Explain the gene duplication event behind dogs with long and short legs
ch18. Gene had a duplication event. A retrotransposon captures a mature RNA and copies it back into RNA. results in an extra copy of the gene with no introns and a very long poly-A tail. Most land at random points that are non-functional but this one has a strong effect on phenotype.
How do new functions replace other ones?
Some amino acids replace other ones, new genes are generated but others are lost. the overall amount of info stays stable.