Asymmetric cell division and differentiation; fern spore germination as a model. II. Ultrastructural studies

Author(s):  
Alix R. Bassel

SynopsisThe germination of Onoclea spores is a model system with many advantages for the study of asymmetric cell division and cellular differentiation. Our results suggest that both microtubules and a lipophilic site are important in the nuclear migration to one end of the spore prior to asymmetric cell division. A metalbinding region containing pore-like structures in the proximal face of the spore coat may be a source of the inherent polarity of the spore. The pattern of endogenous metal binding during germination has been characterised using a sulphide-silver stain. Metal-binding sites are described in a differentiating system in which polarity is imposed externally using polarised red light. The possibility of a role of ion gradients in determining the direction of nuclear migration is discussed.

Author(s):  
John H. Miller

SynopsisDuring germination of Onoclea sensibilis spores, the spore nucleus moves from a central location to one end. Cell division partitions the spore into a small cell which differentiates into a rhizoid, and a larger cell which gives rise, by continued division, to the prothallus. Spore germination is a valuable system in which to study the relationship between asymmetric cell division and the initiation of cell differentiation. It appears that cytoplasmic microtubules and some lipophilic site in the spore are both involved in premitotic nuclear migration. Asymmetric cell division is an obligate step in the initiation of rhizoid differentiation. One hypothesis is that the nucleus must be confined to a small, localised region of the spore for a sufficient time before differentiation can occur, and the confinement is accomplished by the asymmetric cell division. Metal-binding sites are present in the spore coat, specifically on the proximal face. Several types of evidence suggest that the metal-binding region is involved in spore polarity. The sequence of events during germination appears to involve both polarity which is inherent in the spore and polarity which may be imposed by external stimuli. Experiments in which spores are treated with colchicine and polarised red light reveal both types of polarity.


2018 ◽  
Vol 46 (4) ◽  
pp. 797-806 ◽  
Author(s):  
Jessica R. Sanders ◽  
Keith T. Jones

Initiated by luteinizing hormone and finalized by the fertilizing sperm, the mammalian oocyte completes its two meiotic divisions. The first division occurs in the mature Graafian follicle during the hours preceding ovulation and culminates in an extreme asymmetric cell division and the segregation of the two pairs of homologous chromosomes. The newly created mature egg rearrests at metaphase of the second meiotic division prior to ovulation and only completes meiosis following a Ca2+ signal initiated by the sperm at gamete fusion. Here, we review the cellular events that govern the passage of the oocyte through meiosis I with a focus on the role of the spindle assembly checkpoint in regulating its timing. In meiosis II, we examine how the egg achieves its arrest and how the fertilization Ca2+ signal allows the initiation of embryo development.


1987 ◽  
Vol 38 (3) ◽  
pp. 307 ◽  
Author(s):  
HW Higgins ◽  
DJ Mackey

No seasonal variations were found in the concentrations of Zn, Cd, Cu, K, Ca, Mg and Na in the kelp E. radiata collected from the marine-dominated Port Hacking estuary on the east coast of Australia. Concentrations of Fe and Mn were about 60% higher in late summer. The relative distributions of all metals between different kelp tissues, however, showed no seasonal variation. Concentration factors (dry weight basis) for trace metals ranged from 2600 for Cu to 68 000 for Fe. With high biomasses common in macroalgal ecosystems, a large proportion of the non-sediment- bound trace metals can be associated with the macroalgae, which therefore act as substantial buffers for these elements. Metal concentration factors (Y, wet wt basis) were related to oceanic residence times (τ) by the equation log Y = -0.69 logτ + 5.4. The distribution of the aikaii and akaline earth metais (K, Ca, Mg and Na) was relativeiy uniform throughout the various kelp tissues. However, concentrations of Fe, Mn, Zn and Cd were significantly higher in the older extremities (holdfast and eroding tip) than in the meristematic region. Although the holdfast also had higher levels of Cu than the meristem, levels were lower in the eroding tip. The results suggest either a slow net intracellular accumulation of metals with time or an increase in potential metal- binding sites as the extremities senesce. Translocation and elimination of surplus metals through the eroding tip or holdfast was thought not to be important in E. radiata as metal concentrations did not differ between live and dead haptera of the holdfast. Likewise, storage of metals in either the holdfast or eroding tip was considered unlikely because of the constant relative tissue distribution throughout the year and lack of metal mobilization during periods of growth. Pretreatment of kelp tissue with an EDTA wash released about 90% of the total Zn and Cd, 25% of the Cu and 7% of the Fe, suggesting that a large proportion of the total kelp Zn and Cd is associated with the apparent free space (AFS). With rapid exchange between seawater and the AFS, E. radiata is therefore not generally useful as a sentinel accumulator species in pollution studies for assessing long term integrated changes of metals in the water column.


2003 ◽  
Vol 213 (7) ◽  
pp. 328-335 ◽  
Author(s):  
Qian Cheng ◽  
Rachel Fowler ◽  
Lai-wa Tam ◽  
Lisseth Edwards ◽  
Stephen M. Miller

2004 ◽  
Vol 380 (3) ◽  
pp. 805-813 ◽  
Author(s):  
Michael A. CATER ◽  
John FORBES ◽  
Sharon La FONTAINE ◽  
Diane COX ◽  
Julian F. B. MERCER

The Wilson protein (ATP7B) is a copper-transporting CPx-type ATPase defective in the copper toxicity disorder Wilson disease. In hepatocytes, ATP7B delivers copper to apo-ceruloplasmin and mediates the excretion of excess copper into bile. These distinct functions require the protein to localize at two different subcellular compartments. At the trans-Golgi network, ATP7B transports copper for incorporation into apo-ceruloplasmin. When intracellular copper levels are increased, ATP7B traffics to post-Golgi vesicles in close proximity to the canalicular membrane to facilitate biliary copper excretion. In the present study, we investigated the role of the six N-terminal MBSs (metal-binding sites) in the trafficking process. Using site-directed mutagenesis, we mutated or deleted various combinations of the MBSs and assessed the effect of these changes on the localization and trafficking of ATP7B. Results show that the MBSs required for trafficking are the same as those previously found essential for the copper transport function. Either MBS 5 or MBS 6 alone was sufficient to support the redistribution of ATP7B to vesicular compartments. The first three N-terminal motifs were not required for copper-dependent intracellular trafficking and could not functionally replace sites 4–6 when placed in the same sequence position. Furthermore, the N-terminal region encompassing MBSs 1–5 (amino acids 64–540) was not essential for trafficking, with only one MBS close to the membrane channel, necessary and sufficient to support trafficking. Our findings were similar to those obtained for the closely related ATP7A protein, suggesting similar mechanisms for trafficking between copper-transporting CPx-type ATPases.


Biochemistry ◽  
2010 ◽  
Vol 49 (33) ◽  
pp. 7080-7088 ◽  
Author(s):  
Rong Shi ◽  
Christine Munger ◽  
Abdalin Asinas ◽  
Stéphane L. Benoit ◽  
Erica Miller ◽  
...  

2021 ◽  
Vol 83 (4) ◽  
Author(s):  
Sungrim Seirin-Lee

AbstractIn the process of asymmetric cell division, the mother cell induces polarity in both the membrane and the cytosol by distributing substrates and components asymmetrically. Such polarity formation results from the harmonization of the upstream and downstream polarities between the cell membrane and the cytosol. MEX-5/6 is a well-investigated downstream cytoplasmic protein, which is deeply involved in the membrane polarity of the upstream transmembrane protein PAR in the Caenorhabditis elegans embryo. In contrast to the extensive exploration of membrane PAR polarity, cytoplasmic polarity is poorly understood, and the precise contribution of cytoplasmic polarity to the membrane PAR polarity remains largely unknown. In this study, we explored the interplay between the cytoplasmic MEX-5/6 polarity and the membrane PAR polarity by developing a mathematical model that integrates the dynamics of PAR and MEX-5/6 and reflects the cell geometry. Our investigations show that the downstream cytoplasmic protein MEX-5/6 plays an indispensable role in causing a robust upstream PAR polarity, and the integrated understanding of their interplay, including the effect of the cell geometry, is essential for the study of polarity formation in asymmetric cell division.


2014 ◽  
Vol 358 (2) ◽  
pp. 621-626 ◽  
Author(s):  
Hugo Gabilondo ◽  
María Losada-Pérez ◽  
Ignacio Monedero ◽  
Arturo Torres-Herráez ◽  
Isabel Molina ◽  
...  

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