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Sagot :
Complete question:
You will find the pedigree in the attached files
Answer:
The correct option is C) maternal mitochondrial mutations are inherited by all of a mother's offspring.
Explanation:
Mitochondrial inheritance is one of the ways in which a disease or a trait might be inherited from the maternal line.
Most of the DNI is located in the nucleus, but there is also DNI in mitochondria. Sperm cells hardly carry mitochondria, so mitochondrial DNI is mostly inherited from the maternal side. If there exists any mutation in this DNI, the whole progeny of the mutated woman will be affected, as they will get the mother´s mitochondria carrying the mutation. On the contrary, if there is a man affected by a disease caused by a mutation in mitochondrial DNI, non of their descendants will get the disease.
In the exposed pedigree, we can see that the mother is affected by the disease, but the couple had two daughters, and only one of them was affected, while the other one was not. This tells us that the mutation occurred on a nuclear chromosome. If the mutated allele was in mitochondria, both daughters would be affected.
The pedigree suggests that the gene is on a nuclear chromosome, and not on a mitochondrial DNA because maternal mitochondrial mutations are inherited by all of a mother's offspring (Option C).
- Mitochondrial DNA (mtDNA) is a special type of genetic material that exhibits a matrilineal inheritance pattern.
- In consequence, all genes (and mutations) contained in mtDNA will pass from the mother to her offspring.
- It is for that reason that mtDNA is widely used in evolutionary studies (we can trace matrilineal lineage from mtDNA).
In conclusion, the pedigree suggests that the gene is on a nuclear chromosome, and not on a mitochondrial DNA because maternal mitochondrial mutations are inherited by all of a mother's offspring (Option C).
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