What findings led geneticists to postulate the multiple-factor hypothesis that invoked the idea of additive alleles to explain inheritance patterns?
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
20. Quantitative Genetics
Traits and Variance
Problem 5
Textbook Question
The use of nucleotide sequence data to measure genetic variability is complicated by the fact that the genes of many eukaryotes are complex in organization and contain 5' and 3' flanking regions as well as introns. Researchers have compared the nucleotide sequence of two cloned alleles of the γ-globin gene from a single individual and found a variation of 1 percent. Those differences include 13 substitutions of one nucleotide for another and three short DNA segments that have been inserted in one allele or deleted in the other. None of the changes takes place in the gene's exons (coding regions). Why do you think this is so, and should it change our concept of genetic variation?

1
Step 1: Understand the structure of eukaryotic genes, which include exons (coding regions), introns (non-coding regions within genes), and 5' and 3' flanking regions (non-coding sequences adjacent to the gene). Recognize that mutations can occur in any of these regions but may have different effects depending on their location.
Step 2: Consider why nucleotide variations are found only in non-coding regions (introns and flanking regions) and not in exons. This is likely because mutations in exons can alter the amino acid sequence of the protein, potentially affecting its function and being subject to negative selection, whereas mutations in non-coding regions often have less immediate impact on protein function and can accumulate more freely.
Step 3: Reflect on the concept of genetic variation: it includes all differences in DNA sequences, not just those that change protein sequences. Variations in non-coding regions can affect gene regulation, splicing, or other aspects of gene expression, so they are still important for genetic diversity.
Step 4: Analyze how the presence of insertions and deletions (indels) in non-coding regions contributes to genetic variability without necessarily affecting the phenotype, highlighting the complexity of interpreting sequence variation in terms of functional consequences.
Step 5: Conclude that the observation does not diminish the importance of genetic variation but rather emphasizes that genetic variability includes both coding and non-coding changes, and that evolutionary pressures often conserve coding sequences while allowing more variation in non-coding regions.

This video solution was recommended by our tutors as helpful for the problem above
Video duration:
1mPlay a video:
Was this helpful?
Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Gene Structure in Eukaryotes
Eukaryotic genes are composed of exons (coding regions) and introns (non-coding regions), along with 5' and 3' flanking sequences that regulate gene expression. Variations often occur in non-coding regions because they are less likely to affect protein function, allowing more mutations to accumulate without harmful effects.
Recommended video:
Guided course
Chromosome Structure
Types of Genetic Variation
Genetic variation includes nucleotide substitutions, insertions, and deletions. Variations in non-coding regions, such as introns or flanking sequences, may not alter protein sequences but can influence gene regulation or splicing. Understanding these variations helps clarify the full scope of genetic diversity beyond just coding changes.
Recommended video:
Guided course
Genomic Variation
Neutral Theory of Molecular Evolution
This theory proposes that most genetic variations are neutral and do not affect an organism’s fitness, especially those in non-coding regions. The observed 1% variation outside exons supports this idea, indicating that many mutations accumulate without selective pressure, which broadens our understanding of genetic variation beyond functional changes.
Recommended video:
Guided course
Evolution
Related Videos
Related Practice
Textbook Question
486
views