Gujarati
Hindi
4.Principles of Inheritance and Variation
medium

Sickle­cell anaemia is

A

caused by substitution of valine by glutamic acid in the beta globin chain of haemoglobin

B

caused by a change in a single base pair of $DNA$

C

characterized by elongated sickle like $RBCs$ with a nucleus

D

an autosomal linked dominant trait.

(AIPMT-2009)

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 $CCTGTGGAG.$

Standard 12
Biology

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