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 THREE - BRISTLE PATTERNS
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
The epidermis of a D. melanogaster adult has on the order of 500,000 cells, ∼5,000 of which (∼1%) make bristles. A priori, it would seem reasonable to expect bristles to sprout as randomly as the hairs on a human arm. However, even the most scattered bristles – the tergite microchaetes (mCs) – have fairly uniform spacing. At the other extreme of precision are the 40 macrochaetes (MCs) on the head and thorax, whose basic layout has been conserved for 50 million years (Fig. 3.1).
Except for the MCs, the bristles of each body region tend to vary in number and position from one fly to the next. Interestingly, most bristles are organized in rows that run parallel or perpendicular to axes of the body or limbs. Within such rows, the bristles are aligned more or less accurately and are spaced more or less evenly. Different rules govern different patterns. Thus, notal mCs form jagged rows along the anteriorposterior axis, while wing bristles form straight rows along the margin, eye bristles arise at alternating vertices of each ommatidium, and belly (sternital) bristles are spaced at intervals proportional to their shaft lengths.
Why do such patterns exist? Surely, some are adaptive. For example, flies use “brushes” (parallel transverse rows) on the legs to wipe dust from their eyes, and other patterns appear to map air currents, prevent wetting, or act as shock absorbers. However, many may simply be accidents of evolution.
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- Imaginal DiscsThe Genetic and Cellular Logic of Pattern Formation, pp. 31 - 75Publisher: Cambridge University PressPrint publication year: 2002
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