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Positional information: fields, boundaries, and gradients

Positional information: fields, boundaries, and gradients. Development requires a dramatic increase in the amount of information contained within the organism. The "new" information is contained in the genome, and is gradually translated into cellular processes.

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Positional information: fields, boundaries, and gradients

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  1. Positional information: fields, boundaries, and gradients Development requires a dramatic increase in the amount of information contained within the organism. The "new" information is contained in the genome, and is gradually translated into cellular processes. The principal ways in which this happens is by (1) subdivision of larger fields of cells into smaller fields, and (2) specifying the "address" of each cell within the field. This is a recursive process that requires translation of gradients of gene expression into sharp boundaries, and initiation of new gradients by these boundaries

  2. Specification of cell fates Positional cues (Pattern formation): Cell fate is determined by its spatial position within a morphogenetic field during a critical time period Historical cues (Cell lineage): Cell fate is determined by inherited molecules or gene expression states Both mechanisms are required for cell specification, and often act simultaneously.

  3. Y Pattern formation Cell fate Cue 2 Cue 1 X Morphogenetic (progenitor) field is a region or a group of cells that show no overt differentiation, but that is “destined” to give rise to a particular organ or structure. Morphogenetic fields are to some extent autonomous and integrated.

  4. Primary and secondary fields Y etc. X

  5. Morphogen gradients A morphogen is a (usually) secreted molecule that induces cell fate decisions in recipient cells in a concentration-dependent manner Requires: Spatially restricted production Long-range distribution (passive or active) Reception and interpretation Interpretation is context-dependent Most animal morphogens belong to a small number of well-conserved and widely distributed families

  6. Morphogen gradient Source Concentration Positional information Position Positional information may include both scalar and vector components (distance and direction)

  7. Gradients and cell polarity

  8. Wolpert's "French flag" model Single gradient

  9. Wolpert's "French flag" model Double gradient

  10. Signal transduction

  11. Positional information is translated into the activation and repression of target genes Responses to morphogen gradients: activation / repression of target genes; cell proliferation and growth; morphogenetic movements Responses are context-specific

  12. Translating boundary into gradient dpp Boundary of Engrailed expression serves as the source of Hedgehog gradient Hedgehog activates expression of a second morphogen, Dpp, which establishes a bidirectional gradient ci en ci ptc smo ci hh Hh

  13. Translating gradient into boundary

  14. Threshold responses to the Dorsal morphogen gradient sna sog zen

  15. Threshold responses to the Dpp morphogen gradient

  16. Threshold responses to the Dpp morphogen gradient hnt ush (Lost in dpp / - )

  17. After the gradient: Refining position-specific cell fates msh ind vnd

  18. After the gradient: Refining position-specific cell fates Cowden and Levine 2003

  19. Short-range (contact-mediated) signaling Notch signaling

  20. Sensory organ precursor lineage in Drosophila

  21. Interplay of position and lineage

  22. Context-dependent action of morphogen gradients Dorso-ventral Anterior-posterior sna sog zen Same morphogen, different targets, different responses

  23. "Selector genes" provide the context in which positional information is interpreted Act as digital switches that “toggle” between distinct fates Can be induced by morphogens or other selector genes Form multi-layer hierarchies

  24. Signaling pathways activate selector genes… … and vice versa Dpp Wg Distal-less EGFR Target genes, including other selectors and signals

  25. Types of selector genes Spatial region Organ Cell / tissue type

  26. HOX genes and axial patterning

  27. Combinatorial specification of cell fates

  28. Combinatorial control of cell fates Signal 1 Selector A Signal 2 Selector B Target Gene Z Target Gene X Target Gene Y Cell fate l Cell fate y Cell fate z A relatively small “toolkit” of signals and selector genes can specify a wide range of cell fates by a combinatorial mechanism

  29. Control of gene expression by selector genes and signaling pathways Different signal/selector combinations define different cell fates and gene expression domains

  30. Precise spatial control of cell fates Culi and Modolell 1998

  31. Precise spatial control of cell fates Garcia-Garcia et al 1999

  32. Precise spatial control of cell fates Renaud and Simpson 2002

  33. Combinatorial control by overlapping selectors Selector A Selector C Selector B Cell fate 1 Cell fate 5 Cell fate 2 Cell fate 4 Cell fate 3

  34. Axial patterning by overlapping regional determinants Multiple positions along the Proximo-Distal axis are defined by selector genes expressed in overlapping concentric domains

  35. Axial patterning by overlapping regional determinants Kojima 2004

  36. Progressive regionalization of morphogenetic fields

  37. Combinations of regional identities establish new regional identities

  38. Regulatory hierarchies in development

  39. Genes and molecules that control animal development are widely conserved Signaling pathways Hedgehog Notch Dpp/ TGFb Ras/ raf Wingless/ Wnt Jak/ Stat Selector genes HOX genes eyeless/ Pax6 (eye development) Distal-less (appendages) tinman (heart)

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