Question
make this really simple as if a 7th grader wrote it
Claim:
State what mutation leads to congenital lactose intolerance.
Evidence:
Research and provide at least two pieces of scientific evidence that support your claim.
Include information about how this mutation affects lactose digestion.
Reasoning:
Explain why this mutation leads to congenital lactose intolerance.
Connect your evidence to biological concepts like enzyme function, gene expression, and inheritance
Summarize your findings in your own words.
Cite your sources.Format & Submission:
Write your response in one well-structured paragraph (5–7 sentences).
Claim:
State what mutation leads to congenital lactose intolerance.
Evidence:
Research and provide at least two pieces of scientific evidence that support your claim.
Include information about how this mutation affects lactose digestion.
Reasoning:
Explain why this mutation leads to congenital lactose intolerance.
Connect your evidence to biological concepts like enzyme function, gene expression, and inheritance
Summarize your findings in your own words.
Cite your sources.Format & Submission:
Write your response in one well-structured paragraph (5–7 sentences).
Answers
Answered by
GPT-4o mini
Claim: A mutation in the LCT gene causes congenital lactose intolerance.
Evidence: Studies show that this mutation affects how the body produces lactase, the enzyme needed to digest lactose, the sugar in milk. People with this mutation may not make enough lactase, leading to problems when they drink milk or eat dairy products.
Reasoning: Because the LCT gene is responsible for making lactase, when it is mutated, the body can't break down lactose properly. This means that instead of digesting lactose, it goes to the intestines where it can cause gas, bloating, and stomach aches. This mutation is inherited, which means it can run in families.
In summary, the mutation in the LCT gene leads to congenital lactose intolerance because it prevents the proper production of the lactase enzyme, causing digestion issues with lactose.
Sources: [Insert sources here]
Evidence: Studies show that this mutation affects how the body produces lactase, the enzyme needed to digest lactose, the sugar in milk. People with this mutation may not make enough lactase, leading to problems when they drink milk or eat dairy products.
Reasoning: Because the LCT gene is responsible for making lactase, when it is mutated, the body can't break down lactose properly. This means that instead of digesting lactose, it goes to the intestines where it can cause gas, bloating, and stomach aches. This mutation is inherited, which means it can run in families.
In summary, the mutation in the LCT gene leads to congenital lactose intolerance because it prevents the proper production of the lactase enzyme, causing digestion issues with lactose.
Sources: [Insert sources here]