NEETBiologyPrinciples of Inheritance and VariationMCQ+4 / −1
Sickle-cell anemia is :
- ACaused by substitute of valine by glutamic acid in the beta globin chain of haemoglobin
- BAn autosomal linked dominant trait
- CCaused by a change in a single base pair of DNA
- DCharacterized by elongated sickle like RBCs with a nucleus
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Correct answer: C
Sickle-cell anaemia is an autosomal hereditary disorder in which erythrocytes become sickle shaped. It is caused by the formation of abnormal haemoglobin called haemoglobin-S. Haemoglobin-S is formed when 6th amino acid of -chain, i.e., glutamic acid is replaced by valine due to substitution. It occurs due to a single nucleotide change (A T) in the -globin gene of coding strand. In the normal -globin gene the DNA sequence is CCTGAGGAG, while in sicklecell anaemia, the sequence is CCTGTGGAG.
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