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Question
What is the difference between missense and nonsense mutation?
Solution
- Mis-sense Mutation:
The mutation where the codon for one amino acid is changed into a codon for another amino acid is called Missense or non-synonymous mutations. - Non-sense Mutation:
The mutations where the codon for one amino acid is changed into a termination or stop codon is called a Nonsense mutation.
RELATED QUESTIONS
Answer the following question.
Two children, A and B aged 4 and 5 years respectively visited a hospital with a similar genetic disorder. The girl A was provided enzyme-replacement therapy and was advised to revisit periodically for further treatment. The girl, B was, however, given a therapy that did not require revisit for further treatment.
Name the ailments the two girls were suffering from?
Answer the following question.
Two children, A and B aged 4 and 5 years respectively visited a hospital with a similar genetic disorder. The girl A was provided enzyme-replacement therapy and was advised to revisit periodically for further treatment. The girl, B was, however, given a therapy that did not require revisit for further treatment.
Why did the treatment provided to girl A required repeated visits?
Answer the following question.
Two children, A and B aged 4 and 5 years respectively visited a hospital with a similar genetic disorder. The girl A was provided enzyme-replacement therapy and was advised to revisit periodically for further treatment. The girl, B was, however, given a therapy that did not require revisit for further treatment.
How was the girl B cured permanently?
Assertion (A): Gamma rays are generally used to induce mutation in wheat varieties.
Reason (R): Because they carry lower energy to non-ionize electrons from atom
Draw the diagram of different types of aneuploidy.
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Albinism is known to be due to an autosomal recessive mutation. The first child of a couple with normal skin pigmentation was an albino. What is the probability that their second child will also be an albino?
One of the parents of a cross has mutation in its mitochondria. In that cross, that parent is taken as a male. During segregation of F2 progenies that mutation is found in ______.
A change of single base pair in the gene for beta-globin chain (in human haemoglobin) results in the change of amino acid residue glutamic acid to valine which is due to ______
A strong mutagen is:
Mutations result in
How are alleles of particular gene differ from each other? Explain its significance.
Match List I with List II.
| List I | List II | ||
| A. | A pair of chromosomes extra with diploid | i) | monosomy |
| B. | One chromosome extra to the diploid | ii) | tetrasomy |
| C. | One chromosome loses from diploid | iii) | trisomy |
| D. | Two individual chromosomes lose from diploid | iv) | double monosomy |
Match list I with list II.
| List I | List II |
| A. A pair of chromosomes extra with diploid | i) Monosomy |
| B. One chromosome extra to the diploid | ii) Tetrasomy |
| C. One chromosome loses a diploid | iii) Trisomy |
| D. Two individual chromosomes lose their diploid | iv) Double chromosome |
Match list I with list II.
| List I | List II | ||
| A. | A pair of chromosomes extra with diploid | i) | monosomy |
| B. | One chromosome extra to the diploid | ii) | tetrasomy |
| C. | One chromosome loses from diploid | iii) | trisomy |
| D. | Two individual chromosomes lose from diploid | iv) | double monosomy |
Match list I with list II.
| List I | List II | ||
| A. | A pair of chromosomes extra with diploid | i) | monosomy |
| B. | One chromosome extra to the diploid | ii) | tetrasomy |
| C. | One chromosome loses from diploid | iii) | trisomy |
| D. | Two individual chromosomes lose from diploid | iv) | double monosomy |
Match list I with list II
| List I | List II |
| A. A pair of chromosomes extra with diploid | (i) monosomy |
| B. One chromosome extra to the diploid | (ii) tetrasomy |
| C. One chromosome loses from diploid | (iii) trisomy |
| D. Two individual chromosomes lose from diploid | (iv) double monosomy |
Match list I with list II
| List I | List II | ||
| A. | A pair of chromosomes extra with diploid | i) | monosomy |
| B. | One chromosome extra to the diploid | ii) | tetrasomy |
| C. | One chromosome loses from diploid | iii) | trisomy |
| D. | Two individual chromosomes lose from diploid | iv) | double monosomy |
