You have isolated two petite mutants, pet1 and pet2, in Saccharomyces cerevisiae. When pet1 is mated with wild-type yeast, the haploid products following meiosis segregate 2:2 (wild type : petite). In contrast, when pet2 is mated with wild type, all haploid products following meiosis are wild type. To what class of petite mutations does each of these petite mutants belong? What types of progeny do you expect from a pet1 × pet2 mating?
Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
2. Mendel's Laws of Inheritance
Monohybrid Cross
Problem 15
Textbook Question
A woman with severe discoloration of her tooth enamel has four children with a man who has normal tooth enamel. Two of the children, a boy (B) and a girl (G), have discolored enamel. Each has a mate with normal tooth enamel and produces several children. G has six children—four boys and two girls. Two of her boys and one of her girls have discolored enamel. B has seven children—four girls and three boys. All four of his daughters have discolored enamel, but all his boys have normal enamel. Explain the inheritance of this condition.

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Step 1: Begin by analyzing the inheritance pattern of the condition. Severe discoloration of tooth enamel could be inherited in a dominant or recessive manner, and it may be linked to autosomal or sex chromosomes. Examine the data provided for clues about the inheritance mechanism.
Step 2: Observe the woman with discolored enamel and her partner with normal enamel. Two of their children (a boy and a girl) have discolored enamel, suggesting that the condition is not sex-linked but could be autosomal dominant. If it were autosomal recessive, both parents would need to carry the allele, which is not indicated here.
Step 3: Analyze the offspring of G (the daughter with discolored enamel). G has six children—four boys and two girls. Two of her boys and one of her girls have discolored enamel. This suggests that G is heterozygous for the condition, as not all her children inherit the discolored enamel trait.
Step 4: Examine the offspring of B (the son with discolored enamel). B has seven children—four girls and three boys. All four of his daughters have discolored enamel, but all his boys have normal enamel. This pattern strongly suggests that the condition is X-linked dominant, as daughters inherit the X chromosome from their father, while sons inherit the Y chromosome, which does not carry the allele for discolored enamel.
Step 5: Conclude that the inheritance pattern of severe discoloration of tooth enamel is X-linked dominant. The woman with discolored enamel likely has the dominant allele on one of her X chromosomes, which she passes to her children. This explains why her son B passes the condition to all his daughters but none of his sons, and why her daughter G, being heterozygous, passes the condition to some of her children but not all.

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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Autosomal Dominance and Recessiveness
In genetics, traits can be inherited in dominant or recessive patterns. A dominant trait only requires one copy of the allele to be expressed, while a recessive trait requires two copies. In this case, the discoloration of tooth enamel may be a recessive trait, as the father with normal enamel does not express the trait, suggesting he carries a normal allele.
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Variations on Dominance
X-Linked Inheritance
Some traits are linked to the X chromosome, which can affect inheritance patterns, especially in males and females. Males have one X and one Y chromosome, while females have two X chromosomes. If the discoloration is X-linked, it would explain why B's daughters (who inherit his X chromosome) all have the condition, while his sons do not.
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Punnett Squares and Probability
Punnett squares are tools used to predict the probability of offspring inheriting particular traits based on the genotypes of the parents. By analyzing the genotypes of the parents in this scenario, one can determine the likelihood of their children inheriting the discoloration trait, helping to clarify the inheritance pattern observed in the children.
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