Damien Broderick <damien@ariel.ucs.unimelb.edu.au> writes:
> Everyone knows that DNA is prey to mutations, most of them quickly edited
> out by vigilant repair mechanisms, most of the rest neutral or bad news,
> only a few improving the genes they happen to occur within. But by what
> chemical pathway do those mutations come about? I'd always assumed that
> most of them involved gross *deletions* of one or more nucleotide bases,
> the implication being that the least dangerous deletion would knock out
> three adjacent bases in one go (otherwise *all* the subsequent three-letter
> codons are fouled). However, many mutations occur at a single point. The
> classic instance is the change creating sickle cell anaemia, in which
> position 6 in the 146 amino acid chain has valine instead of glutamic acid.
> Presumably this means that an adenine has been changed into a uracil (or,
> in the DNA chain, into a thymine).
>
> But how the hell does the equivalent of a random impact do that?
(But I do run Avida, an artificial life program, in another window)
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