Developmental biology

Source: Wikipedia, the free encyclopedia.

Developmental biology is the study of the process by which animals and plants grow and develop. Developmental biology also encompasses the biology of regeneration, asexual reproduction, metamorphosis, and the growth and differentiation of stem cells in the adult organism.

Perspectives

The main processes involved in the

regional specification and patterned cell differentiation); tissue growth; and tissue morphogenesis
.

The development of plants involves similar processes to that of animals. However, plant cells are mostly immotile so morphogenesis is achieved by differential growth, without cell movements. Also, the inductive signals and the genes involved are different from those that control animal development.

Generative biology

Generative biology is the generative science that explores the dynamics guiding the development and evolution of a biological morphological form.[1][2][3]

Developmental processes

Cell differentiation

The Notch-delta system in neurogenesis (Slack Essential Dev Biol Fig 14.12a)

HNF4
for hepatocyte differentiation. Cell differentiation is usually the final stage of development, preceded by several states of commitment which are not visibly differentiated. A single tissue, formed from a single type of progenitor cell or stem cell, often consists of several differentiated cell types. Control of their formation involves a process of lateral inhibition,[6] based on the properties of the Notch signaling pathway.[7] For example, in the neural plate of the embryo this system operates to generate a population of neuronal precursor cells in which NeuroD is highly expressed.

Regeneration

urodele amphibians.[13]
Considerable information is now available about amphibian limb regeneration and it is known that each cell type regenerates itself, except for connective tissues where there is considerable interconversion between cartilage, dermis and tendons. In terms of the pattern of structures, this is controlled by a re-activation of signals active in the embryo. There is still debate about the old question of whether regeneration is a "pristine" or an "adaptive" property.[14] If the former is the case, with improved knowledge, we might expect to be able to improve regenerative ability in humans. If the latter, then each instance of regeneration is presumed to have arisen by natural selection in circumstances particular to the species, so no general rules would be expected.

Embryonic development of animals

Generalized scheme of embryonic development. Slack "Essential Developmental Biology". Fig. 2.8.
human embryogenesis

The sperm and egg fuse in the process of fertilization to form a fertilized egg, or

blastula or blastoderm. These cell divisions are usually rapid with no growth so the daughter cells are half the size of the mother cell and the whole embryo stays about the same size. They are called cleavage
divisions.

Mouse

embryogenesis”) undergo extensive epigenetic reprogramming.[16] This process involves genome-wide DNA demethylation, chromatin reorganization and epigenetic imprint erasure leading to totipotency.[16] DNA demethylation is carried out by a process that utilizes the DNA base excision repair pathway.[17]

Morphogenetic movements convert the cell mass into a three layered structure consisting of multicellular sheets called

germ layers. This is the process of gastrulation. During cleavage and gastrulation the first regional specification events occur. In addition to the formation of the three germ layers themselves, these often generate extraembryonic structures, such as the mammalian placenta, needed for support and nutrition of the embryo,[18] and also establish differences of commitment along the anteroposterior axis (head, trunk and tail).[19]

transcription factors which upregulate new combinations of gene activity in each region. Among other functions, these transcription factors control expression of genes conferring specific adhesive and motility properties on the cells in which they are active. Because of these different morphogenetic properties, the cells of each germ layer move to form sheets such that the ectoderm ends up on the outside, mesoderm in the middle, and endoderm on the inside.[23][24]

Schema of the development of the axial twist in vertebrates

Morphogenetic movements not only change the shape and structure of the embryo, but by bringing cell sheets into new spatial relationships they also make possible new phases of signaling and response between them. In addition, first morphogenetic movements of embryogenesis, such as gastrulation,

chordates (including vertebrates) and is addressed by the axial twist theory.[28]

Growth in embryos is mostly autonomous.[29]
For each territory of cells the growth rate is controlled by the combination of genes that are active. Free-living embryos do not grow in mass as they have no external food supply. But embryos fed by a placenta or extraembryonic yolk supply can grow very fast, and changes to relative growth rate between parts in these organisms help to produce the final overall anatomy.

The whole process needs to be coordinated in time and how this is controlled is not understood. There may be a master clock able to communicate with all parts of the embryo that controls the course of events, or timing may depend simply on local causal sequences of events.[30]

Metamorphosis

Developmental processes are very evident during the process of metamorphosis. This occurs in various types of animal. Well-known examples are seen in frogs, which usually hatch as a tadpole and metamorphoses to an adult frog, and certain insects which hatch as a larva and then become remodeled to the adult form during a pupal stage.

All the developmental processes listed above occur during metamorphosis. Examples that have been especially well studied include tail loss and other changes in the tadpole of the frog Xenopus,[31][32] and the biology of the imaginal discs, which generate the adult body parts of the fly Drosophila melanogaster.[33][34]

Plant development

Plant development is the process by which structures originate and mature as a plant grows. It is studied in plant anatomy and plant physiology as well as plant morphology.

Plants constantly produce new tissues and structures throughout their life from meristems[35] located at the tips of organs, or between mature tissues. Thus, a living plant always has embryonic tissues. By contrast, an animal embryo will very early produce all of the body parts that it will ever have in its life. When the animal is born (or hatches from its egg), it has all its body parts and from that point will only grow larger and more mature.

The properties of organization seen in a plant are emergent properties which are more than the sum of the individual parts. "The assembly of these tissues and functions into an integrated multicellular organism yields not only the characteristics of the separate parts and processes but also quite a new set of characteristics which would not have been predictable on the basis of examination of the separate parts."[36]

Growth

A

embryogenesis. As this happens, the resulting cells will organize so that one end becomes the first root, while the other end forms the tip of the shoot. In seed plants, the embryo will develop one or more "seed leaves" (cotyledons
). By the end of embryogenesis, the young plant will have all the parts necessary to begin its life.

Once the embryo

In addition to growth by cell division, a plant may grow through cell elongation.[39] This occurs when individual cells or groups of cells grow longer. Not all plant cells will grow to the same length. When cells on one side of a stem grow longer and faster than cells on the other side, the stem will bend to the side of the slower growing cells as a result. This directional growth can occur via a plant's response to a particular stimulus, such as light (phototropism), gravity (gravitropism), water, (hydrotropism), and physical contact (thigmotropism).

Plant growth and development are mediated by specific plant hormones and plant growth regulators (PGRs) (Ross et al. 1983).[40] Endogenous hormone levels are influenced by plant age, cold hardiness, dormancy, and other metabolic conditions; photoperiod, drought, temperature, and other external environmental conditions; and exogenous sources of PGRs, e.g., externally applied and of rhizospheric origin.

Morphological variation

Plants exhibit natural variation in their form and structure. While all organisms vary from individual to individual, plants exhibit an additional type of variation. Within a single individual, parts are repeated which may differ in form and structure from other similar parts. This variation is most easily seen in the leaves of a plant, though other organs such as stems and flowers may show similar variation. There are three primary causes of this variation: positional effects, environmental effects, and juvenility.

Evolution of plant morphology

Transcription factors and transcriptional regulatory networks play key roles in plant morphogenesis and their evolution. During plant landing, many novel transcription factor families emerged and are preferentially wired into the networks of multicellular development, reproduction, and organ development, contributing to more complex morphogenesis of land plants.[41]

Most land plants share a common ancestor, multicellular algae. An example of the evolution of plant morphology is seen in charophytes. Studies have shown that charophytes have traits that are homologous to land plants. There are two main theories of the evolution of plant morphology, these theories are the homologous theory and the antithetic theory. The commonly accepted theory for the evolution of plant morphology is the antithetic theory. The antithetic theory states that the multiple mitotic divisions that take place before meiosis, cause the development of the sporophyte. Then the sporophyte will development as an independent organism.[42]

Developmental model organisms

Much of developmental biology research in recent decades has focused on the use of a small number of

model organisms
. It has turned out that there is much conservation of developmental mechanisms across the animal kingdom. In early development different vertebrate species all use essentially the same inductive signals and the same genes encoding regional identity. Even invertebrates use a similar repertoire of signals and genes although the body parts formed are significantly different. Model organisms each have some particular experimental advantages which have enabled them to become popular among researchers. In one sense they are "models" for the whole animal kingdom, and in another sense they are "models" for human development, which is difficult to study directly for both ethical and practical reasons. Model organisms have been most useful for elucidating the broad nature of developmental mechanisms. The more detail is sought, the more they differ from each other and from humans.

Plants

Vertebrates

Invertebrates

Unicellular

Others

Also popular for some purposes have been

urodele amphibians such as the axolotl Ambystoma mexicanum are used,[53] and also planarian worms such as Schmidtea mediterranea.[10] Organoids have also been demonstrated as an efficient model for development.[54] Plant development has focused on the thale cress Arabidopsis thaliana as a model organism.[55]

See also

References

  1. .
  2. ^ "Generative Biology: Designing Biologic Medicines with Greater Speed and Success". Amgen. June 7, 2022. Retrieved 5 April 2024.
  3. ^ "Generative Biology: Learning to Program Cellular Machines". NIH. Mar 15, 2024. Retrieved 5 April 2024.
  4. PMID 17320508
    .
  5. .
  6. (PDF) from the original on 2017-10-27.
  7. .
  8. ^ Carlson BM (2007). Principles of Regenerative Biology. Burlington MA: Academic Press.
  9. PMID 17234176
    .
  10. ^ .
  11. .
  12. .
  13. .
  14. ^ Slack JM (2013). "Chapter 20". Essential Developmental Biology. Oxford: Wiley-Blackwell.
  15. PMID 12941269
    .
  16. ^ .
  17. .
  18. ^ Steven DH, ed. (1975). Comparative Placentation. London: Academic Press.
  19. PMID 23801439
    .
  20. .
  21. .
  22. .
  23. .
  24. .
  25. .
  26. .
  27. .
  28. .
  29. ^ O'Farrell PH (2003). "How metazoans reach their full size: the natural history of bigness.". In Hall MN, Raff M, Thomas G (eds.). Cell Growth: Control of Cell Size. Cold Spring Harbor Laboratory Press. pp. 1–21.
  30. S2CID 29029979
    .
  31. .
  32. .
  33. ^ Cohen SM (1993). "Imaginal Disc Development.". In Bate M, Martinez-Arias M (eds.). The Development of Drosophila melanogaster. Cold Spring Harbor Press.
  34. PMID 14550411
    .
  35. .
  36. ^ Leopold AC (1964). Plant Growth and Development. New York: McGraw-Hill. p. 183.
  37. S2CID 5833219
    .
  38. .
  39. .
  40. ^ Ross SD, Pharis RP, Binder WD (1983). "Growth regulators and conifers: their physiology and potential uses in forestry.". In Nickell LG (ed.). Plant growth regulating chemicals. Vol. 2. Boca Raton, FL: CRC Press. pp. 35–78.
  41. from the original on 2016-06-02.
  42. .
  43. ^ .
  44. ^ Nieuwkoop PD, Faber J (1967). Normal table of Xenopus laevis (Daudin). North-Holland, Amsterdam.{{cite book}}: CS1 maint: location missing publisher (link)
  45. PMID 21963197
    .
  46. .
  47. .
  48. ^ Behringer R, Gertsenstein M, Vintersten K, Nagy M (2014). Manipulating the Mouse Embryo. A Laboratory Manual (Fourth ed.). Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.
  49. S2CID 195368351
    .
  50. ^ Riddle DL, Blumenthal T, Meyer BJ, Priess JR (1997). C.elegans II. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.
  51. PMID 10948448. {{cite book}}: |journal= ignored (help
    )
  52. .
  53. .
  54. .
  55. ^ Weigel D, Glazebrook J (2002). Arabidopsis. A Laboratory Manual. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.

Further reading

External links