Positional information and pattern formation

2017 ◽  
pp. 198-230 ◽  
Author(s):  
L. Wolpert
1974 ◽  
Vol 15 (2) ◽  
pp. 321-346 ◽  
Author(s):  
H. MEINHARDT ◽  
A. GIERER

Model calculations are presented for various problems of development on the basis of a theory of primary pattern formation which we previously proposed. The theory involves short-range autocatalytic activation and longer-range inhibition (lateral inhibition). When a certain criterion is satisfied, self-regulating patterns are generated. The autocatalytic features of the theory are demonstrated by simulations of the determination of polarity in the Xenopus retina. General conditions for marginal and internal activation, and corresponding effects of symmetry are discussed. Special molecular mechanisms of pattern formation are proposed in which activator is chemically converted into inhibitor, or an activator precursor is depleted by conversion into activator. The (slow) effects of primary patterns on differentiation can be included into the formalism in a straightforward manner. In conjunction with growth, this can lead to asymmetric steady states of cell types, cell differentiation and proliferation as found, for instance, in growing and budding hydra. In 2 dimensions, 2 different types of patterns can be obtained. Under some assumptions, a single pattern-forming system produces a ‘bristle’ type pattern of peaks of activity with rather regular spacings on a surface. Budding of hydra is treated on this basis. If, however, gradients develop under the influence of a weak external or marginal asymmetry, a monotonic gradient can be formed across the entire field, and 2 such gradient-forming systems can specify ‘positional information’ in 2 dimensions. If inhibitor equilibrates slowly, a spatial pattern may oscillate, as observed with regard to the intracellular activation of cellular slime moulds. The applications are intended to demonstrate the ability of the proposed theory to explain properties frequently encountered in developing systems.


Development ◽  
1975 ◽  
Vol 33 (2) ◽  
pp. 511-521
Author(s):  
J. Hicklin ◽  
A. Hornbruch ◽  
L. Wolpert

The dynamics of regions away from the head-end boundary have been investigated by avariety of assays, and the changes appear to be slow. If, for example, a head end is graftedonto a peduncle to give H/56F, region 5 does not become a region 1 within 72 h. Suchresults support a gradient type model, and exclude a head end inducing a region 1 in thetissue adjacent to it. The changes can be interpreted if the positional value were effectivelyslowly diffusible: about 10 times more slowly than the positional signal. These results alsohave implications for studies on polarity reversal.


Development ◽  
1979 ◽  
Vol 50 (1) ◽  
pp. 175-198
Author(s):  
L. Wolpert ◽  
C. Tickle ◽  
M. Sampford ◽  
J. H. Lewis

It has been suggested that positional information along the proximo-distal axis of the limb-bud is specified by time spent in the progress zone. Mesenchyme cells have been killed by X-irradiation, reducing the rate cells leave the zone. The time spent there by some cells is thus increased. When limbs, stage 18/19, stage 21, or tips of stage 24, are treated with increasing doses of X-irradiation, from 1000 rads to 2500 rads proximal structures are progressively lost, whereas distal ones— the digits—are relatively unaffected. There was no evidence for intercalation of missing parts. These effects are due to killing or damage of mesenchyme cells: the ectoderm is not affected at these doses. The results are consistent with a quantitative analysis based on the progress zone model, in which viable cells repopulate the progress zone and gradually restore it to normal as non-dividing cells are diluted out. It is suggested that any treatment causing damage to the mesenchyme at early stages will give similar results. The mesenchyme cells appear to be surprisingly resistant to radiation damage. The form of the limb-bud is not altered by damaging the mesenchyme. Differences in the development of structures at similar proximo-distal levels, following irradiation, is considered in terms of the requirement of a threshold number of cells.


Development ◽  
2020 ◽  
Vol 147 (23) ◽  
pp. dev196394
Author(s):  
Tirtha Das Banerjee ◽  
Antónia Monteiro

ABSTRACTHow mechanisms of pattern formation evolve has remained a central research theme in the field of evolutionary and developmental biology. The mechanism of wing vein differentiation in Drosophila is a classic text-book example of pattern formation using a system of positional information, yet very little is known about how species with a different number of veins pattern their wings, and how insect venation patterns evolved. Here, we examine the expression pattern of genes previously implicated in vein differentiation in Drosophila in two butterfly species with more complex venation Bicyclus anynana and Pieris canidia. We also test the function of some of these genes in B. anynana. We identify both conserved as well as new domains of decapentaplegic, engrailed, invected, spalt, optix, wingless, armadillo, blistered and rhomboid gene expression in butterflies, and propose how the simplified venation in Drosophila might have evolved via loss of decapentaplegic, spalt and optix gene expression domains, via silencing of vein-inducing programs at Spalt-expression boundaries, and via changes in expression of vein maintenance genes.


1980 ◽  
Vol 35 (11-12) ◽  
pp. 1086-1091 ◽  
Author(s):  
Hans Meinhardt

Abstract A mechanism is proposed for pattern formation in developmental subfields. In application to imaginal disks, the compartmentalization appears as a prerequisite for the generation of positional information in the proximo-distal dimension. Cooperation of three or four compartments in the production of a morphogen leads to a cone-shaped morphogen distribution, since a high production rate of the morphogen is possible only at the intersection of compartment borders. The local concentration of the cone-shaped distribution is a measure for the distance from this center and can be used as positional information. In agreement with the experimental observations, the model predicts that (i) the distalmost structures are formed at the intersection of compartment borders; (ii) distal transformation occurs whenever cells of all compartments come close to each other; (iii) distal transformation does not require a complete set of circumferential structures; (iv) mutants exist in which the positional information and not the response of the cells is altered and (v) no distal to proximal intercalation of missing leg segments occur. Regeneration and formation of supernumerary insect legs can be explained as well. Simple molecular reaction can account for this type of pattern formation. The “complete circle rule” of French, Bryant and Bryant (Science 193,969-981 (1976)) for distal transformation may be simplified by a “cooperation of compartments” rule.


Development ◽  
1981 ◽  
Vol 63 (1) ◽  
pp. 127-144
Author(s):  
J. C. Smith ◽  
L. Wolpert

A study is made of the widening of the chick limb bud that occurs after a graft of an additional polarizing region. Such buds are about 50% wider than controls, after 36 h. By contrast, growth along the proximodistal axis is unaffected. This widening is reduced by treating the host embryo with 10 Gy X-irradiation and the altered pattern of digits is consistent with a diffusible morphogen model for the specification of positional information along the anteroposterior axis.


Sign in / Sign up

Export Citation Format

Share Document