Genomics and mutation explore the variations in our genetic code and their impact on health and evolution. This topic covers different types of mutations, from single nucleotide substitutions to large scale chromosomal changes, and their phenotypic consequences. Students also investigate the field of genomics, including how genome sequencing is used in modern medicine. This is a rapidly evolving area of the MOE syllabus, reflecting the growing importance of genetics in society.
MOE Syllabus OutcomesMOE Syllabus 9744 Core Idea 2(e)MOE Syllabus 9744 Core Idea 2(f)
Groups are given a 'normal' DNA sequence and several 'mutated' versions. They must transcribe and translate each one to determine which mutations are silent, missense, or nonsense, and then predict the impact on the protein's function.
How does the lac operon function in the presence and absence of lactose?
The class is divided into groups representing different stakeholders (scientists, ethicists, patients, government). They must debate a specific scenario, such as using CRISPR to eliminate a hereditary disease in Singapore, considering both the benefits and the risks.
What are the roles of general and specific transcription factors in eukaryotes?
Stations feature different genomic applications, such as personalized medicine for cancer, tracing ancestry, or agricultural improvements. Students rotate to each station, taking notes on how genomics is being used and identifying any potential ethical concerns.
How does chromatin remodeling affect the accessibility of genes for transcription?
Students often believe that all mutations are harmful.
Explain that many mutations are neutral (silent mutations) and some can even be beneficial, providing the raw material for evolution. A 'mutation sorting' activity where students categorize mutations as 'harmful,' 'neutral,' or 'beneficial' can help broaden their perspective.
There is a common belief that a mutation in one cell will automatically be passed on to offspring.
Clarify the distinction between somatic mutations (which only affect the individual) and germline mutations (which can be passed to offspring). Discussing real-world examples like skin cancer versus hereditary conditions can help reinforce this point.