Gene mutations (CIE International A-level Biology)

This fully-resourced lesson explains how gene mutations can occur by substitution, deletion and insertion and explores how these base pair changes can affect the primary structure of the polypeptide and therefore the phenotype. The engaging and detailed PowerPoint and accompanying resources have been designed to cover point 16.2 (e) of the CIE International A-level Biology specification which states that students should understand how these mutations occur and can affect the phenotype.

In order to understand how a change in the base sequence can affect the order of the amino acids, students must be confident in their understanding and application of protein synthesis which was taught in topic 6. Therefore, the start of the lesson focuses on transcription and translation and students are guided through the use of the codon table to identify amino acids. Moving forwards, a quick quiz competition is used to introduce the names of three types of gene mutation whilst challenging the students to recognise terms which are associated with the genetic code and were met in the previous lesson. The main focus of the lesson is base substitutions and how these mutations may or may not cause a change to the amino acid sequence. The students are challenged to use their knowledge of the degenerate nature of the genetic code to explain how a silent mutation can result. The rest of the lesson looks at base deletions and base insertions and students are introduced to the idea of a frameshift mutation. One particular task challenges the students to evaluate the statement that base deletions have a bigger impact on primary structure than base substitutions. This is a differentiated task and they have to compare the fact that the reading frame is shifted by a deletion against the change in a single base by a substitution