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Use appropriate genetic cross to explain: XX-XY XX-XO methods of sex determination. (12 mrks)

Biology

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5. (a) Non-disjunction occurred in sex chromosomes of man. Show the genotype and phenotype of their offspring with Klinefelter's Syndrome.
Non-disjunction is the failure of homologous chromosomes or sister chromatids to separate properly during meiosis. If non-disjunction of the X chromosomes occurs in the mother during oogenesis, an egg with two X chromosomes (XXXX) can be formed. If this XXXX egg is then fertilized by a normal Y sperm from the father, the resulting offspring will have Klinefelter's Syndrome.

  1. Consider the gametes from parents where non-disjunction has occurred.

    • Mother (due to non-disjunction): Produces an XXXX egg.
    • Father (normal): Produces XX or YY sperm.
  2. Fertilization leading to Klinefelter's Syndrome.

    If the XXXX egg from the mother is fertilized by a normal YY sperm from the father:

    • Offspring genotype: XXYXXY
    • Offspring phenotype: Male with Klinefelter's Syndrome (characterized by features such as reduced fertility, taller stature, and some feminized physical traits).

    5. (b) A carrier of haemophilia marries a normal male. Show the chances of their offspring getting haemophiliac.
    Haemophilia is an X-linked recessive disorder. Let XHX^H be the normal allele and XhX^h be the haemophilia allele.

    • Carrier female genotype: XHXhX^H X^h
    • Normal male genotype: XHYX^H Y
  3. Determine the gametes produced by each parent.

    • Female (XHXhX^H X^h): Gametes are XHX^H and XhX^h.
    • Male (XHYX^H Y): Gametes are XHX^H and YY.
  4. Construct a Punnett square.

    XHYXHXHXHXHYXhXHXhXhY\begin{array}{|c|c|c|} \hline & X^H & Y \\ \hline X^H & X^H X^H & X^H Y \\ \hline X^h & X^H X^h & X^h Y \\ \hline \end{array}
  5. Determine the genotypes and phenotypes of the offspring.

    • XHXHX^H X^H: Normal female
    • XHYX^H Y: Normal male
    • XHXhX^H X^h: Carrier female
    • XhYX^h Y: Haemophiliac male
  6. Calculate the chance of their offspring getting haemophiliac.

    Only the XhYX^h Y genotype results in a haemophiliac child.
    The chance of having a haemophiliac child is 14\frac{1}{4}.

    The chance of their offspring getting haemophiliac is 25%\boxed{\text{25\%}}.

    5. (c) State two factors that are revealed in a blood group test.

    • The specific ABO blood type (e.g., A, B, AB, or O).
    • The Rh factor status (positive or negative).
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