Introduction to Evolutionary Conservation
Mutations occur spontaneously in each generation, randomly changing the amino acid sequences of proteins. Individuals with mutations that impair critical functions of proteins may have resulting problems that make them less able to reproduce. Harmful mutations are lost from the gene pool because the individuals carrying them reproduce less effectively. Over time, only harmless (or very rare beneficial) mutations are maintained in the gene pool. This is evolution.
Examples
Consider the protein methyl CpG binding protein 2 (MeCP2). Although its function is still unclear, it is expressed throughout the body, and disruption of its function causes problems with brain development and function[1]. Some mutations in MeCP2 cause Rett Syndrome, a severely debilitating condition affecting mostly women.
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V.
Introduction to Multiple Sequence Alignment (MSA) and Conservation
ConSurf Server
Structure of Atomic Coordinate ("PDB") Files
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<a href="https://www.proteopedia.org/wiki/index.php/Conservation%2C_Evolutionary"
target="_blank">Evolutionary conservation</a>
identifies functional sites in protein molecules.
Effect of mutation on protein function
Genetic consequence
Example
Function LOST**
CONSERVED:
mutation LOST from gene poolR133C*
None
NOT conserved:
mutation remains in gene poolE143?*
- in methyl CpG binding protein 2 (MeCP2),
<a href="https://www.proteopedia.org/wiki/index.php/3c2i" target="_blank">3c2i</a>:
ASASPKQRRS IIRDRGPMYD DPTLPEGWTR KLKQRKSGRS AGKYDVYLIN
PQGKAFRSKV ELIMYFEKVG DTSLDPNDFD FTVTGRGSPS RHHHHHH
^ ^
- R133C causes
<a href="slides/rett/rett.htm" target="_blank">Rett syndrome,</a> a severe neurological disorder.
Gray: disordered in crystal, absent in model 3c2i.Notes and References
- ↑ MECP2 article in the National Library of Medicine's Genetic Home Reference