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Explore the intricate process of order in biological systems emerging from noisy molecular processes. Delve into the spatial pattern formation during the early embryonic development of Drosophila melanogaster. Discover the significant events within the first 3 hours post-fertilization, including nuclear divisions, morphological changes, and the critical process of gastrulation. Witness how maternal gradients influence gene activities and identity determination in the embryo. Uncover the complex interactions between key proteins like Bicoid and Hunchback that regulate spatial patterning. From the activation of gap genes to segment polarity genes, follow the precise orchestration of gene expressions during development. This study provides insights into the establishment of gradients, morphogen movement, and cellular responses to concentration variations, offering a quantitative approach to understanding biological pattern formation.
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How does order in biological systems arise from molecular processes which are intrinsically noisy? or How to form spatial pattern? Noise, precision, diffusion and scaling in biological pattern formation
Life cycle of Drosophila melanogaster Life cycle
Early Embryonic Development (first 3 hours) First 3 hours fertilization 13 rounds of nuclear divisions syncytium, no cells yet ~6000 cells form after 2h morphologic cell shape changes after 3h (gastrulation)
Gastrulation Gastrulation Identical cells 15 minutes later Cells display distinct behaviors
Maternal gradients determine early embryonic gene activity Dorsal Nanos Bicoid Torso Torso ~6000 nuclei need to know their identity from 4 maternal gradients
Bcd-hb activation Bicoid RNA deposited at anterior end of egg is translated into Bicoid protein, which is thought to diffuse along the length of the egg, establishing a gradient Bicoid RNA Bicoid protein Bicoid protein activates Hunchback gene expression
Bicoid protein is a “transcription factor” that enters the nucleus, binds to and activates transcription of other genes One example is the “Hunchback” gene
Bicoid protein activatesgap genes Threshold readout Final distribution reflects simple physical parameters (diffusion, degradation) Bicoid protein Activation ofHunchbackandKruppeloccurs wherever Bicoid protein is above acritical threshold Information is Quantitative Response depends on concentration levels Hunchback HunchbackKrüppel
Intro genes maternal gradient bicoid Gap genes hunchback Pair rule genes runt Segment polarity genes wingless
Final observed precision is at the level of one nuclear spacing Even-skipped Runt Head fold initiates in single row of yellow cells
larva Embryo (~3h) Larva (~24h)
Need more quantitative approach to address these questions… bicoid
Model based on 3 assumptions: • Constant source at head pole • Diffusion • Uniform degradation D = diffusion constant t = protein lifetime Concentration Steady state: 0% 100% Position(m) Hunchback (Hb) Activation of hb occurs wherever Bcd is above a certain threshold Bicoid protein activates hunchback gene Bicoid turns on hunchback Bicoid protein (Bcd)
Dipteran eggs vary greatly in size Calliphora (blow fly) ~1500mm Drosophila melanogaster ~480mm Lucilia ~1200mm Drosophila busckii ~320mm Musca (housefly) ~1200mm
questions How are gradients established?How do morphogen molecules move? Can simple physical mechanisms produce the required accuracy? How do cells “read” small differences in concentrations?How reproducible are these decisions Are responses always on/off?
Nuclear Stainings Cycle 9 Cycle 11 Cycle 13 Cycle 14
The response to the Bicoid gradient (hunchback trans-cription) is precise and invariant despite Bicoid variability Bicoid Hunchback B. Houchmandzadeh, E. Wieschaus, S. Leibler, Nature, 2002