Contrast the XX/XY and XX/X0 modes of sex determination.
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
3. Extensions to Mendelian Inheritance
Sex Chromosome
Problem 8
Textbook Question
What specific observations (evidence) support the conclusions about sex determination in Drosophila and humans?
Verified step by step guidance1
Identify the key differences in sex determination mechanisms between Drosophila and humans. In Drosophila, sex is determined by the ratio of X chromosomes to sets of autosomes (X:A ratio), whereas in humans, sex is determined by the presence or absence of the Y chromosome.
Examine experimental evidence in Drosophila, such as the observation that flies with two X chromosomes and two sets of autosomes (X:A = 1) develop as females, while those with one X chromosome and two sets of autosomes (X:A = 0.5) develop as males. This supports the role of the X:A ratio in sex determination.
Consider genetic studies in humans showing that individuals with XY chromosomes develop as males due to the presence of the SRY gene on the Y chromosome, which triggers male development, while individuals with XX chromosomes develop as females. This highlights the importance of the Y chromosome in human sex determination.
Look at cases of sex reversal or intersex conditions in both species, such as XX males or XY females in humans, and how these cases provide evidence for the genetic basis of sex determination (e.g., translocation of SRY gene). In Drosophila, changes in the X:A ratio can lead to intersex phenotypes, further supporting the ratio model.
Summarize that the specific observations supporting sex determination conclusions include chromosome counts, phenotypic sex outcomes, and genetic manipulations or mutations that alter expected sex development patterns in both Drosophila and humans.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Chromosomal Basis of Sex Determination
Sex determination in both Drosophila and humans is governed by specific chromosomes, known as sex chromosomes. In humans, the presence of XX chromosomes typically results in females, and XY in males. In Drosophila, the ratio of X chromosomes to sets of autosomes determines sex, with XX being female and XY male. Observations of chromosome patterns in offspring support these mechanisms.
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Sex Determination
Genetic Evidence from Mutant and Aneuploid Individuals
Studies of individuals with abnormal numbers or structures of sex chromosomes, such as Turner syndrome (XO) or Klinefelter syndrome (XXY) in humans, and similar chromosomal variants in Drosophila, provide evidence for how sex chromosomes influence sexual development. These genetic anomalies help clarify the role of specific chromosomes in sex determination.
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Experimental Crosses and Phenotypic Ratios
Controlled breeding experiments in Drosophila and pedigree analyses in humans reveal patterns of inheritance and sex ratios that support chromosomal sex determination. For example, observing the sex ratios in offspring from specific crosses or families helps confirm the role of sex chromosomes and the mechanisms by which they determine sex.
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