Germ band differentiation in the stomatopod Gonodactylaceus falcatus and the origin of the stereotyped cell division pattern in Malacostraca (Crustacea)

2010 ◽  
Vol 39 (6) ◽  
pp. 411-422 ◽  
Author(s):  
Antje H.L. Fischer ◽  
Tino Pabst ◽  
Gerhard Scholtz
Author(s):  
Gerhard Scholtz

Beginning with Aristotle 2400 years ago, research on crustacean embryology has a long tradition. Rathke’s 1829 landmark study on the noble crayfish initiated modern approaches. Crustaceans in general—and most of their large taxa—show a great diversity in all stages of their developmental pathways from the zygote up to the adult animal. This chapter describes the various modes of cleavage, gastrulation, germ band formation, and segmentation found in crustacean taxa. Cleavage is either total, partial, or mixed. Total cleavage can be indeterminate, without predictable cell lineage; or determinate, with a stereotyped cell division pattern. Gastrulation modes can also vary to a high degree. One finds invagination, epiboly, immigration, delamination, and a mix of some of these. Likewise, the stages of germ layer separation and the number of cells that initiate gastrulation differ. In yolk-rich eggs, a germ disk forms at the future ventral side of the embryo, and the axes and orientation of the germ are recognizable. Through elongation in the anteroposterior direction by a posterior growth zone and intercalary cell divisions, the germ disk is transformed into the germ band. As a result of a unique, stereotyped cell division pattern in the germ band of malacostracans, germ band growth and the segmentation process up to the differentiation of neuronal precursors and early limb anlagen can be analyzed at the level of individual cells. Recent morphological and molecular techniques allow a very detailed spatiotemporal resolution of developmental processes and they offer new perspectives on long-standing morphological questions.


Development ◽  
1989 ◽  
Vol 107 (2) ◽  
pp. 201-212 ◽  
Author(s):  
N.H. Patel ◽  
T.B. Kornberg ◽  
C.S. Goodman

We have used a monoclonal antibody that recognizes engrailed proteins to compare the process of segmentation in grasshopper, crayfish, and Drosophila. Drosophila embryos rapidly generate metameres during an embryonic stage characterized by the absence of cell division. In contrast, many other arthropod embryos, such as those of more primitive insects and crustaceans, generate metameres gradually and sequentially, as cell proliferation causes caudal elongation. In all three organisms, the pattern of engrailed expression at the segmented germ band stage is similar, and the parasegments are the first metameres to form. Nevertheless, the way in which the engrailed pattern is generated differs and reflects the differences in how these organisms generate their metameres. These differences call into question what role homologues of the Drosophila pair-rule segmentation genes might play in other arthropods that generate metameres sequentially.


Development ◽  
1990 ◽  
Vol 110 (4) ◽  
pp. 1319-1325 ◽  
Author(s):  
A.P. Gould ◽  
R.Y. Lai ◽  
M.J. Green ◽  
R.A. White

The Polycomb (Pc) gene is required from the extended germ band stage onwards, to maintain spatially restricted patterns of homeotic gene expression. It has been thought to be involved in the ‘stable inheritance of the determined state’. In this paper, we have tested the notion that the Pc gene is required specifically during or after DNA replication to enable the stable transmission of states of gene activity. We found that arresting cell division using the string mutation or blocking DNA replication with aphidicolin failed to prevent ectopic expression of the homeotic gene Ultrabithorax in Pc mutants. Thus, even in the absence of DNA replication, Pc is required to maintain spatially restricted patterns of homeotic gene expression. The role of the Pc gene product in the stable repression of homeotic gene transcription is discussed.


2019 ◽  
Vol 116 (42) ◽  
pp. 21285-21290 ◽  
Author(s):  
Rongfeng Huang ◽  
Rui Zheng ◽  
Jun He ◽  
Zimin Zhou ◽  
Jiacheng Wang ◽  
...  

In both plants and animals, multiple cellular processes must be orchestrated to ensure proper organogenesis. The cell division patterns control the shape of growing organs, yet how they are precisely determined and coordinated is poorly understood. In plants, the distribution of the phytohormone auxin is tightly linked to organogenesis, including lateral root (LR) development. Nevertheless, how auxin regulates cell division pattern during lateral root development remains elusive. Here, we report that auxin activates Mitogen-Activated Protein Kinase (MAPK) signaling via transmembrane kinases (TMKs) to control cell division pattern during lateral root development. Both TMK1/4 and MKK4/5-MPK3/6 pathways are required to properly orient cell divisions, which ultimately determine lateral root development in response to auxin. We show that TMKs directly and specifically interact with and phosphorylate MKK4/5, which is required for auxin to activate MKK4/5-MPK3/6 signaling. Our data suggest that TMK-mediated noncanonical auxin signaling is required to regulate cell division pattern and connect auxin signaling to MAPK signaling, which are both essential for plant development.


2017 ◽  
Author(s):  
Marina Linardić ◽  
Siobhan A. Braybrook

AbstractIn plants and parenchymatous brown algae the body arises through the activity of an apical meristem (a niche of cells or a single cell). The meristem produces lateral organs in specific patterns, referred to as phyllotaxis. In plants, two different control mechanisms have been proposed – one is position-dependent and relies on morphogen accumulation at future organ sites whereas the other is a lineage-based system which links phyllotaxis to the apical cell division pattern. Here we examine the apical patterning of the brown alga, Sargassum muticum, which exhibits spiral phyllotaxis (137.5° angle) and an unlinked apical cell division pattern. The Sargassum apex presents characteristics of a self-organising system, similar to plant meristems. We were unable to correlate the plant morphogen auxin with bud positioning in Sargassum, nor could we predict cell wall softening at new bud sites. Our data suggests that in Sargassum muticum there is no connection between phyllotaxis and the apical cell division pattern indicating a position-dependent patterning mechanism may be in place. The underlying mechanisms behind the phyllotactic patterning appear to be distinct from those seen in plants.SummaryThe brown alga Sargassum muticum displays spiral phyllotaxis developed from a position-dependent self-organising mechanism, different from that understood in plants.


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