The most striking example of point mutation is found in a disease called:
Correct answer: B. Sickle cell anaemia
- A. Down's syndrome
- B. Sickle cell anaemia
- C. Thalassaemia
- D. Night blindness
Explanation
Point mutation involves only the replacement of one nucleotide with another. One type of point mutation is missense mutation. These are base changes that alter the codon for an amino acid resulting in its substitution with a different amino acid. For example, mutation of the codon CTT to ATT would result in the replacement of the hydrophobic amino acid leucine with isoleucine, another hydrophobic amino acid. Many other missense mutations have been described which do affect the encoded protein and result in genetic diseases. These include an A to T mutation in the gene for B-globin, one of the polypeptides of hemoglobin. This mutation changes codon six of the gene from GAG which encodes glutamic acid to GTG which encodes valine. The mutation results in a condition called sickle cell anemia.
Report an error
The more specific you are, the faster it gets fixed. A source beats an opinion.
Prefer email? [email protected]
About Inheritance
Mendel's laws explain segregation, independent assortment and the prediction of genetic ratios using alleles, genotypes and phenotypes. The chapter also covers linked genes, recombination and crossing over during meiosis, then applies pedigree reasoning to X-linked recessive traits, which show different inheritance patterns in males and females.
Practise Inheritance
1,238 free Inheritance MCQs from Biology, each with the correct answer and an explanation. Unlimited attempts, no account needed.
Discussion
Stuck on an option, or know a faster way to get there? Ask or explain it here.
No comments yet. Be the first to explain this one.
Exams that ask Biology questions like this
Biology is on 8 papers prepared for on TestUstad, and all of them draw the same bank, so this question is worth knowing for every one of them.
More Inheritance questions
The phenomenon, in which an allele of one gene suppresses the activity of an allele of another gene, is known as:
When two genetic loci produce identical phenotypes in cis and trans position, they are considered to be:
A person whose father is colour blind marries a lady whose mother is daughter of a colour blind man. Their children will be:
The genes, which remain confined to differential region of Y-chromosome, are:
A child's blood group is 'O'. The parent's blood groups cannot be:
The colour blindness is more likely to occur in males than in females because: