English

Jacob is genetically a carrier of the disorder that affects the shape of the RBCs, as shown in the diagram below. His son James suffers from the same disorder.

Advertisements
Advertisements

Question

Jacob is genetically a carrier of the disorder that affects the shape of the RBCs, as shown in the diagram below. His son James suffers from the same disorder.

  1. Give the biochemical reason for the disorder that changes the shape of the RBCs, as shown above.
  2. Draw a Punnett square to show the genotype of the mother of James.
  3. Name and define the type of 'point mutation' responsible for this disorder.
Short/Brief Note
Advertisements

Solution

  1. Red blood cells take on a sickle-like structure when oxygen tension is lowered since the deoxygenated sickle cell haemoglobin (HbS) molecules polymerize to form long fibres.
  2. Given Jacob is a carrier, his genotype has to be HbA HbS.

    James, Jacob's child, suffers with the condition; so, his genotype is HbS HbS.

    According to the provided data, James must inherit one HbS allele from each parent if he is to have sickle call anaemia (HbS HbS). Given Jacob's known carrier status (HbAHbS), he most certainly passed on the HbS gene to James. James's need for two HbS alleles requires the mother to have likewise supplied a HbS allele. The condition (HbS HbS) or a carrier (HbA HbS) can have an impact on the mother.

    Case 1. When mother is a carrier (HbA HbS)

                       Mother

      HbA   HbS
    HbA
    Jacob
    HbA HbA
    (Normal)
    HbA HbS
    (Carrier)
    HbS HbA HbS
    [Carrier]
    HbS HbS
    [Sickle cell]

    James will suffer from a disorder.

    Case 2. When mother is affected (HbS HbS)

                       Mother

      HbS   HbS
    HbA
    Jacob
    HbA HbS
    (Carrier)
    HbA HbS
    (Carrier)
    HbS HbS HbS
    [Sickle cell]
    HbS HbS
    [Sickle cell]

    James will suffer from a disorder.

  3. A monogenetic condition, sickle cell anaemia is caused by a single base-pair point mutation in the β globin gene, substituting glutamic acid for valine in the β-globin chain.
shaalaa.com
  Is there an error in this question or solution?
2023-2024 (March) official

Video TutorialsVIEW ALL [2]

RELATED QUESTIONS

Why are color-blindness and thalassaemia categorised as Mendelian disorders? Write the symptoms of these diseases seen in people suffering from them.


Given below is the representation of amino acid composition not the relevant translated portion of β-chain of haemoglobin, related to the shape of human red blood cells

(a) Is this representation indicating a normal human or a sufferer from certain related genetic disease? Give reason in support of your answer.

(b) What difference would be noticed in the phenotype of the normal and the sufferer related to this gene?

(c) Who are likely to suffer more from the defect related to the gene represented the males, the females or both males and females equally? And why?


Identify I and II in the given diagram of chromosome.


A woman with albinic father marries an albinic man. The proportion of her progeny is ______.


Where are the genes for cytoplasmic male sterility in plants located?


Females with Turner’s syndrome have ______.


Placed below is a karyotype of a human being.

On the basis of this karyotype, which of the following conclusions can be drawn: ______ 


Why is thalassemia cotegorised as a Mendelian disorder? Write the symptoms and explain the causes of the disease. How does it differ from Sickle cell anaemia?


Match the disorder in column I with their nature in column II.

  Column I   Column II
i. Thalassemia a. X monosomy
ii. Turner’s syndrome b. Extra X chromosomes in male
iii. Klinefelter’s syndrome c. 21st Trisomy
iv. Down’s syndrome d. Mendelian disorder

Trisomy of 21st chromosome leads to a disorder ______.


Share
Notifications

Englishहिंदीमराठी


      Forgot password?
Use app×