The male has a mutation in his mittochondria During segregation , the mutation is found in

Options

A. None of the progeny
B. One third of progeny
C. Half of progeny
D. Whole of progeny

Answer

To solve the question regarding the mutation in the mitochondria of a male and its segregation in progeny, we can follow these steps:

### Step-by-Step Solution:

1. **Understanding Mitochondrial Inheritance**:
- Mitochondrial DNA is inherited maternally. This means that only the egg (female gamete) contributes mitochondria to the offspring. The sperm (male gamete) does not contribute mitochondria.

2. **Identifying the Source of Mutation**:
- In this case, the mutation is present in the mitochondria of the male. Since the male does not contribute mitochondria to the offspring, the mutation will not be passed on.

3. **Analyzing Progeny Contribution**:
- Since only the female contributes mitochondria to the progeny, if the male has a mutation in his mitochondria, it will not affect the progeny at all.

4. **Conclusion**:
- Therefore, the mutation found in the male's mitochondria will not be present in any of the progeny.

5. **Final Answer**:
- The correct answer to the question is "none of the progeny".