Book contents
- Frontmatter
- Contents
- Preface
- CHAPTER ONE CELL LINEAGE VS. INTERCELLULAR SIGNALING
- CHAPTER TWO THE BRISTLE
- CHAPTER THREE BRISTLE PATTERNS
- CHAPTER FOUR ORIGIN AND GROWTH OF DISCS
- CHAPTER FIVE THE LEG DISC
- CHAPTER SIX THE WING DISC
- CHAPTER SEVEN THE EYE DISC
- CHAPTER EIGHT HOMEOSIS
- EPILOGUE
- APPENDIX ONE Glossary of Protein Domains
- APPENDIX TWO Inventory of Models, Mysteries, Devices, and Epiphanies
- APPENDIX THREE Genes That Can Alter Cell Fates Within the (5-Cell) Mechanosensory Bristle Organ
- APPENDIX FOUR Genes That Can Transform One Type of Bristle Into Another or Into a Different Type of Sense Organ
- APPENDIX FIVE Genes That Can Alter Bristle Number by Directly Affecting SOP Equivalence Groups or Inhibitory Fields
- APPENDIX SIX Signal Transduction Pathways: Hedgehog, Decapentaplegic, and Wingless
- APPENDIX SEVEN Commentaries on the Pithier Figures
- References
- Index
CHAPTER SEVEN - THE EYE DISC
Published online by Cambridge University Press: 03 December 2009
- Frontmatter
- Contents
- Preface
- CHAPTER ONE CELL LINEAGE VS. INTERCELLULAR SIGNALING
- CHAPTER TWO THE BRISTLE
- CHAPTER THREE BRISTLE PATTERNS
- CHAPTER FOUR ORIGIN AND GROWTH OF DISCS
- CHAPTER FIVE THE LEG DISC
- CHAPTER SIX THE WING DISC
- CHAPTER SEVEN THE EYE DISC
- CHAPTER EIGHT HOMEOSIS
- EPILOGUE
- APPENDIX ONE Glossary of Protein Domains
- APPENDIX TWO Inventory of Models, Mysteries, Devices, and Epiphanies
- APPENDIX THREE Genes That Can Alter Cell Fates Within the (5-Cell) Mechanosensory Bristle Organ
- APPENDIX FOUR Genes That Can Transform One Type of Bristle Into Another or Into a Different Type of Sense Organ
- APPENDIX FIVE Genes That Can Alter Bristle Number by Directly Affecting SOP Equivalence Groups or Inhibitory Fields
- APPENDIX SIX Signal Transduction Pathways: Hedgehog, Decapentaplegic, and Wingless
- APPENDIX SEVEN Commentaries on the Pithier Figures
- References
- Index
Summary
Compound eyes have ∼750 facets, with 8 photoreceptors per facet
A fly's face is dominated by its eyes (Fig. 7.1). Each of the two compound eyes is a honeycomb matrix of ∼750 “ommatidial” subunits. Each subunit, in turn, has 8 photoreceptors or “R” cells (R1–R8) for a total of ∼6,000 receptors per eye. At this pixel density, flies see grainier images than humans, who have ≥ 100,000 receptor cells in the fovea alone. Because fly and human eyes appear to have had a common evolutionary origin, the obvious “One Eye or Many? Riddle” is: Did our common ancestor have a simple or a compound eye? If the former, then why/how did insects multiply it? If the latter, then why/how did chordates reduce it to a solitary remnant? Of course, there is a third possibility. Our common ancestor might have had only a primitive light detector, and we chordate or arthropod descendants then built our own versions of eyes based on the genes that were active at those spots on our face.
The epithelium of the eye disc is a monolayer (as is true for all discs; cf. Ch. 4), but the epithelium of the adult eye is stratified. Above the bundle of 8 R cells, each adult ommatidium has 4 “cone” cells that secrete the lens (no relation to vertebrate cones). Between the bundles are pigment cells that prevent blurring by absorbing scattered photons: 2 PPCs, 6 SPCs, and 3 TPCs (primary, secondary, and tertiary pigment cells) per ommatidium.
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- Imaginal DiscsThe Genetic and Cellular Logic of Pattern Formation, pp. 197 - 236Publisher: Cambridge University PressPrint publication year: 2002
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