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Sicklecell anaemia is
caused by substitution of valine by glutamic acid in the beta globin chain of haemoglobin
caused by a change in a single base pair of $DNA$
characterized by elongated sickle like $RBCs$ with a nucleus
an autosomal linked dominant trait.
Solution
(b) : Sicklecell anaemia is an autosomal hereditary Yellow green disorder in which erythrocytes become sickle shaped. It is caused by the formation ofabnormal haemoglobin called haemoglobin-$S$. Haemoglobin-$S$ is formed when $6^{th}$ amino acid of $\beta$-chain, $i.e.$, glutamic acid is replaced by valine due to substitution. It occurs due to a single nucleotide change $(A → T)$ in the $\beta$-globin gene of coding strand. In the normal $\beta$-globin gene the $DNA$ sequence is $CCTGAGGAG$, while in sickle cell anaemia, the sequence is $CCTGTGGAG.$