Early development in Drosophila is atypical in that pattern formation takes place in a syncytial blastoderm, allowing free diffusion of transcription factors between nuclei. In many other animal species, the fertilized egg is divided by cellular cleavages into a larger and larger number of smaller and smaller cells.
How must the model that describes Drosophila development be modified for describing animal species whose early development is not syncytial?
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
14. Genetic Control of Development
Developmental Patterning Genes
Problem 5
Textbook Question
Consider the even-skipped regulatory sequences in Figure 18.9.
How are the sharp boundaries of expression of eve stripe 2 formed?

1
Understand that the sharp boundaries of expression of eve stripe 2 are formed through the interaction of transcriptional activators and repressors binding to specific regulatory sequences in the DNA.
Identify the activators involved in the regulation of eve stripe 2. These activators, such as Bicoid and Hunchback, bind to the enhancer region of the eve gene and promote transcription in specific regions of the embryo.
Recognize the role of repressors, such as Giant and Kruppel, which bind to the same regulatory region and inhibit transcription in areas where they are expressed, creating sharp boundaries.
Analyze the spatial distribution of these activators and repressors in the embryo. The overlapping gradients of these proteins ensure that eve stripe 2 is expressed only in a narrow band where activators are present and repressors are absent.
Conclude that the sharp boundaries of eve stripe 2 expression are a result of the precise balance and spatial distribution of activators and repressors, which interact with the regulatory sequences to control gene expression in a highly localized manner.

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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Regulatory Sequences
Regulatory sequences are regions of DNA that control the expression of genes. They can include enhancers, silencers, and promoters, which interact with transcription factors to modulate gene activity. In the context of the even-skipped (eve) gene, these sequences are crucial for determining where and when the gene is expressed during development.
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Transcription Factors
Transcription factors are proteins that bind to specific DNA sequences to regulate gene expression. They can act as activators or repressors, influencing the transcription of target genes. In the case of eve stripe 2, specific transcription factors bind to the regulatory sequences, creating sharp boundaries of expression by either promoting or inhibiting transcription in adjacent regions.
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Positional Information and Morphogens
Positional information refers to the spatial cues that cells use to determine their fate during development. Morphogens are signaling molecules that create concentration gradients, providing this positional information. In the formation of eve stripe 2, morphogen gradients help establish the precise boundaries of gene expression by influencing the activity of transcription factors in a spatially restricted manner.
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