Introduction to Evolutionary Conservation

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'''[[3c2i]''':
'''[[3c2i]''':
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<span style="font-size:200%; font-family:monospace;"><font color="gray">&nbsp;&nbsp;&nbsp;ASASPKQRRS IIRD</font>RGPMYD
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<span style="font-size:170%; font-family:monospace;"><font color="gray">&nbsp;&nbsp;&nbsp;ASASPKQRRS IIRD</font>RGPMYD
DPTLPEGWTR KLKQRKSGRS AGKYDVYLIN
DPTLPEGWTR KLKQRKSGRS AGKYDVYLIN
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&nbsp;** R133C causes
&nbsp;** R133C causes
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[http://workshops.molviz.org/slides/rett/rett.htm Rett syndrome],</a>
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[http://workshops.molviz.org/slides/rett/rett.htm Rett syndrome],
a severe neurological disorder.
a severe neurological disorder.
<br>
<br>

Revision as of 22:43, 30 September 2012

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; UniProt MECP2_HUMAN). 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.


Effect of mutation on protein function

Genetic consequence

Example

Function LOST**

CONSERVED:
mutation LOST from gene pool

R133C*

None

NOT conserved:
mutation remains in gene pool

E143?*

 * in methyl CpG binding protein 2 (MeCP2), [[3c2i]:

   ASASPKQRRS IIRDRGPMYD DPTLPEGWTR KLKQRKSGRS AGKYDVYLIN
   PQGKAFRSKV ELIMYFEKVG DTSLDPNDFD FTVTGRGSPS RHHHHHH
         ^          ^
 ** R133C causes Rett syndrome, a severe neurological disorder.
Gray: disordered in crystal, absent in model 3c2i.

Notes and References

  1. ↑ MECP2 article in the National Library of Medicine's Genetic Home Reference

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