The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Biological pattern formation: from basic mechanisms to complex structures
Abstract
The reliable development of highly complex organisms is an intriguing and fascinating problem. The genetic material is, as a rule, the same in each cell of an organism. How then do cells, under the influence of their common genes, produce spatial patterns? Simple models are discussed that describe the generation of patterns out of an initially nearly homogeneous state. They are based on nonlinear interactions of at least two chemicals and on their diffusion. The concepts of local autocatalysis and of long-range inhibition play a fundamental role. Numerical simulations show that the models account for many basic biological observations such as the regeneration of a pattern after excision of tissue or the production of regular (or nearly regular) arrays of organs during (or after) completion of growth. Very complex patterns can be generated in a reproducible way by hierarchical coupling of several such elementary reactions. Applications to animal coats and to the generation of polygonally shaped patterns are provided. It is further shown how to generate a strictly periodic pattern of units that themselves exhibit a complex and polar fine structure. This is illustrated by two examples: the assembly of photoreceptor cells in the eye of Drosophila and the positioning of leaves and axillary buds in a growing shoot. In both cases, the substructures have to achieve an internal polarity under the influence of some primary pattern-forming system existing in the fly's eye or in the plant. The fact that similar models can describe essential steps in organisms as distantly related as animals and plants suggests that they reveal some universal mechanisms.
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Cites
The chemical basis of morphogenesis
Turing, A. M. (1952) · Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences · doi:10.1098/rstb.1952.0012 · Cited by 11,733
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Cited by
Mechanisms of ectodermal organogenesis.
Pispa, J., & Thesleff, I. (2003) · Developmental Biology · doi:10.1016/s0012-1606(03)00325-7 · Cited by 499
Leaf Vascular Pattern Formation.
Nelson, T., & Dengler, N. (1997) · The Plant Cell · doi:10.1105/tpc.9.7.1121 · Cited by 371
Odd dynamics of living chiral crystals
Tan, T. H., Mietke, A., Li, J., Chen, Y., Higinbotham, H., Foster, P. J., Gokhale, S., Dunkel, J., & Fakhri, N. (2022) · Nature · doi:10.1038/s41586-022-04889-6 · Cited by 280
Wenzel, C. L., Schuetz, M., Yu, Q., & Mattsson, J. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02977.x · Cited by 267
How the zebrafish gets its stripes
Rawls, J. F., Mellgren, E. M., & Johnson, S. L. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0418 · Cited by 165
Metadata
- Authors
- Koch, A. J., & Meinhardt, H.
- Venue
- Reviews of Modern Physics
- Publisher
- American Physical Society (APS)
- Published
- 1994-10-01
- Volume
- 66
- Issue
- 4
- Pages
- 1481-1507
- ISSN
- 0034-6861 (ISSN-L)
- 1539-0756
- OpenAlex
- W1982088462
- Cited by
- 677
- References
- 3
- FWCI
- 12.17
- Type
- journal article
- Language
- en
- Open access
- closed
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.