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Analyze the provided pedigree chart: identify diagram type, count females, count affected F1 males, and determine Kate's genotype.
Biology
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7 stepsQuestion 3.1.1
Identify the type of diagram.
The diagram illustrates the inheritance pattern of a genetic trait across multiple generations within a family.
- The type of diagram shown is a pedigree chart.
Question 3.1.2
Count all individuals represented by circles in the pedigree chart.
- Generation I: 2 females (Kate and her sister)
- Generation II: 2 females (Helen and her sister)
- Generation III: 2 females (daughters of Helen and Ben)
- There are a total of 6 females in this family.
Question 3.1.3
Identify the F1-generation and count affected males.
The F1-generation consists of the children of the initial parents (Steve and Kate), which is the second row of individuals. Males are represented by squares, and affected individuals are shaded.
- In the F1-generation, there are two males. One is Ben (unaffected, unshaded). The other is Ben's brother (affected, shaded).
- 1 male in the F1-generation has Goltz syndrome.
Question 3.1.4
Determine Kate's genotype based on the given information and the pedigree.
Goltz syndrome is a sex-linked dominant disorder (allele X). Unaffected individuals have the recessive allele X.
- Kate is an affected female (shaded circle).
- Kate's father, Steve, is an unaffected male (unshaded square), so his genotype is XY.
- Since Kate inherited an X chromosome from her father, she must have inherited X from Steve.
- As Kate is affected, she must also possess the dominant allele X.
- Therefore, Kate's genotype is .
Question 3.1.5
Determine the genotypes of Helen and Ben.
- Helen is an unaffected female (unshaded circle). Since Goltz syndrome is dominant, an unaffected female must be homozygous recessive: XX.
- Ben is an unaffected male (unshaded square). His genotype is XY.
Determine the possible genotypes of their sons.
Sons inherit an X chromosome from their mother and a Y chromosome from their father.
- Helen (XX) can only pass an X chromosome to her sons.
- Ben (XY) passes a Y chromosome to his sons.
- Therefore, all sons will have the genotype XY.
State the phenotype of their sons.
- A genotype of XY means the individual does not have the dominant allele for Goltz syndrome.
- The phenotype of their sons will be unaffected.
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