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1 Analyze the pedigree chart and determine the phenotype and genotype of Senzo and Thuli, and explain the inheritance of colour-blindness.

Biology

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Answer

b

XDXd\text{X}^{\text{D}}\text{X}^{\text{d}}

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Here are the solutions to your questions:

Part 25.1

Part a· 2 steps

  1. Identify Senzo in the pedigree chart.

    Senzo is represented by a filled square.

  2. Refer to the key.

    A filled square indicates a colour-blind male.
    The phenotype of Senzo is:

    • Colour-blind male

Part b

XDXd\text{X}^{\text{D}}\text{X}^{\text{d}}

  1. Identify Thuli in the pedigree chart.

    Thuli is a normal female.

  2. Analyze Thuli's offspring.

    Thuli has a colour-blind daughter, Linda (XdXd\text{X}^{\text{d}}\text{X}^{\text{d}}), and a colour-blind son, Senzo (XdY\text{X}^{\text{d}}\text{Y}).

  3. For Linda to be colour-blind (XdXd\text{X}^{\text{d}}\text{X}^{\text{d}}), she must inherit one Xd\text{X}^{\text{d}} allele from her father and one Xd\text{X}^{\text{d}} allele from her mother (Thuli).

  4. Since Thuli is phenotypically normal but passed on an Xd\text{X}^{\text{d}} allele, she must be a carrier.

    The genotype of Thuli is:

    • XDXd\boxed{\text{X}^{\text{D}}\text{X}^{\text{d}}}

Part 25.2

Linda is a colour-blind female, meaning her genotype is XdXd\text{X}^{\text{d}}\text{X}^{\text{d}}. She inherited one Xd\text{X}^{\text{d}} allele from her mother, Thuli (XDXd\text{X}^{\text{D}}\text{X}^{\text{d}}), and the other Xd\text{X}^{\text{d}} allele from her father (XdY\text{X}^{\text{d}}\text{Y}).

Part 25.3

Colour-blindness is a sex-linked recessive disorder carried on the X chromosome. Males have only one X chromosome (XY\text{XY}), so if they inherit the recessive allele (Xd\text{X}^{\text{d}}), they will express the disorder. Females have two X chromosomes (XX\text{XX}), meaning they need to inherit two copies of the recessive allele (XdXd\text{X}^{\text{d}}\text{X}^{\text{d}}) to be colour-blind. If a female inherits only one recessive allele, she is a carrier but has normal vision due to the dominant allele on her other X chromosome. This makes it statistically more likely for males to be colour-blind.

Part 25.4· 3 steps

  1. Determine Molly's genotype.

    Molly is a normal female. Her mother is Thuli (XDXd\text{X}^{\text{D}}\text{X}^{\text{d}}) and her father is a colour-blind male (XdY\text{X}^{\text{d}}\text{Y}). Molly must have inherited XD\text{X}^{\text{D}} from her mother and Xd\text{X}^{\text{d}} from her father. So, Molly's genotype is XDXd\text{X}^{\text{D}}\text{X}^{\text{d}}.

  2. Determine the normal male's genotype.

    A normal male has the genotype XDY\text{X}^{\text{D}}\text{Y}.

  3. Perform a genetic cross (Punnett square) between Molly (XDXd\text{X}^{\text{D}}\text{X}^{\text{d}}) and a normal male (XDY\text{X}^{\text{D}}\text{Y}).

    Parents: XDXd\text{X}^{\text{D}}\text{X}^{\text{d}} (Molly) ×\times XDY\text{X}^{\text{D}}\text{Y} (Normal male)

    Gametes from Molly: XD\text{X}^{\text{D}}, Xd\text{X}^{\text{d}}
    Gametes from Normal Male: XD\text{X}^{\text{D}}, Y\text{Y}

     XDYXDXDXDXDYXdXDXdXdY\begin{array}{|c|c|c|} \hline \text{ } & \text{X}^{\text{D}} & \text{Y} \\ \hline \text{X}^{\text{D}} & \text{X}^{\text{D}}\text{X}^{\text{D}} & \text{X}^{\text{D}}\text{Y} \\ \hline \text{X}^{\text{d}} & \text{X}^{\text{D}}\text{X}^{\text{d}} & \text{X}^{\text{d}}\text{Y} \\ \hline \end{array}

    Possible Genotypes and Phenotypes of their children:

    • Genotypes:

      • 1/41/4 XDXD\text{X}^{\text{D}}\text{X}^{\text{D}}
      • 1/41/4 XDXd\text{X}^{\text{D}}\text{X}^{\text{d}}
      • 1/41/4 XDY\text{X}^{\text{D}}\text{Y}
      • 1/41/4 XdY\text{X}^{\text{d}}\text{Y}
    • Phenotypes:

      • 1/21/2 Normal females (1/41/4 homozygous normal, 1/41/4 carrier)
      • 1/41/4 Normal males
      • 1/41/4 Colour-blind males
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