Nonsense mutation: Difference between revisions
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Nonsense mutation is when there is a nucleotide substitution causing a different [[ | Nonsense mutation is when there is a nucleotide substitution causing a different [[Amino acid|amino acid]] to be coded for, which creates a [[Stop codon|stop codon]] . This causes the protein that is being encoded for to be truncated due to the premature termination of [[Translation|translation]].<sup><span style="display: none" id="1322760910616S"> </span></sup><sup>[1]</sup> | ||
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<u>'''References'''</u> | <u>'''References'''</u> | ||
<sup>[1] </sup>Hartl, D. and Jones, E. (2009) Genetics, U.S.A: Jones and Bartlett | <sup>[1] </sup>Hartl, D. and Jones, E. (2009) Genetics: Genes and Genomes, U.S.A: Jones and Bartlett, page 515 | ||
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Revision as of 17:51, 1 December 2011
Nonsense mutation is when there is a nucleotide substitution causing a different amino acid to be coded for, which creates a stop codon . This causes the protein that is being encoded for to be truncated due to the premature termination of translation.[1]
References
[1] Hartl, D. and Jones, E. (2009) Genetics: Genes and Genomes, U.S.A: Jones and Bartlett, page 515