Pollen Wall Substructure and Development inTanacetum vulgare(Compositae: Anthemideae): Revisiting Hypotheses on Pattern Formation in Complex Cell Walls

2016 ◽  
Vol 177 (4) ◽  
pp. 347-370 ◽  
Author(s):  
Nina I. Gabarayeva ◽  
Valentina V. Grigorjeva ◽  
Stephen Blackmore
2004 ◽  
Vol 79 (7) ◽  
pp. 729-733 ◽  
Author(s):  
Peiqiang Yu ◽  
John J McKinnon ◽  
David D Maenz ◽  
Vern J Racz ◽  
David A Christensen

2011 ◽  
Vol 2011 ◽  
pp. 1-11 ◽  
Author(s):  
Beda M. Yapo

Rhamnogalacturonan II (RG-II) is a type of block copolymer of complex pectins that represents a quantitatively minor component of the primary cell walls of land (vascular) plants. The structural composition of RG-II is almost totally sequenced and appears to be remarkably conserved in all tracheophytes so far examined. The backbone of RG-II, released from complex (cell wall) pectins by endo-polygalacturonase (Endo-PG) treatment, has been found to contain up to 15 (1→4)-linked-α-D-GalpA units, some of which carry four well-defined side chains, often referred to as A-, B-, C-, and D-side chains. Nevertheless, the relative locations on the backbone of these four branches, especially the A chain, remain to be ascertained. A combination of different data suggests that neither the terminal nonreducing GalA nor the contiguous GalA unit is likely to be the branching point of the A chain, but probably the ninth GalA residue from the reducing end, assuming a minimum backbone length of 11 (1→4)-linked-α-d-GalpA. The latest reports on RG-II are here highlighted, with a provided update for the macrostructure and array of functionalities.


2013 ◽  
Vol 162 (2) ◽  
pp. 720-731 ◽  
Author(s):  
Jun Yang ◽  
Lei Tian ◽  
Ming-Xi Sun ◽  
Xue-Yong Huang ◽  
Jun Zhu ◽  
...  

1974 ◽  
Vol 52 (6) ◽  
pp. 1209-1214 ◽  
Author(s):  
R. A. Fischer ◽  
J. Dainty ◽  
M. T. Tyree

We present a quantitative ultrastructural study of the size and frequency (density distribution) of plasmodesmata in the cell wall in common between the internodal cell and peripheral cell (and central cell) of Chara corallina. In the wall in common between the central cell and internodal cell the relative area occupied by plasmodesmata is 15.3%; the pore diameter (less the plasmalemma) is 118 nm; the length is 1.54 μm, and the frequency is 1.4 × 109 pores/cm2. In the wall in common between the peripheral cell and internodal cell the relative area occupied by the plasmodesmata is 9.6%; the pore diameter is 100 nm; the length is 1.07 μm; and the frequency is 1.2 × 109 pores/cm2. The plasmodesmata have an anastomosing structure like Nitella translucens but the pore diameter and frequency are much greater.


Science ◽  
2004 ◽  
Vol 306 (5705) ◽  
pp. 2160f-2160f
Keyword(s):  

Author(s):  
René Schneider ◽  
Kris van ’t Klooster ◽  
Kelsey Picard ◽  
Jasper van der Gucht ◽  
Taku Demura ◽  
...  

ABSTRACTPlants are the tallest organisms on Earth; a feature sustained by solute-transporting xylem vessels in the plant vasculature. The xylem vessels are supported by strong cell walls that are assembled in intricate patterns. Cortical microtubules direct wall deposition and need to rapidly re-organize during xylem cell development. We established long-term live-cell imaging of single Arabidopsis cells undergoing proto-xylem trans-differentiation, resulting in spiral wall patterns, to investigate the microtubule re-organization. The initial disperse microtubule array rapidly readjusted into well-defined microtubule bands, which required local de-stabilization of individual microtubules in band-interspersing gap regions. Using extensive microtubule simulations, we could recapitulate the process in silico and found that local recruitment of microtubule-bound nucleation is critical for pattern formation, which we confirmed in vivo. Our simulations further indicated that the initial microtubule alignment impact microtubule band patterning. We confirmed this prediction using katanin mutants, which have microtubule organization defects, and uncovered active KATANIN recruitment to the forming microtubule bands. Our combination of quantitative microscopy and modelling outlines a framework towards a comprehensive understanding of microtubule re-organization during wall pattern formation.


HortScience ◽  
1992 ◽  
Vol 27 (6) ◽  
pp. 642a-642
Author(s):  
Carlos A. Perez-Munoz ◽  
Barbara D. Webster

During the initiation of pollen exine wall formation in Vigna, localized accumulations of membranes in the microspore cortex coincide with sites which during further development reflect the lumina of me reticulate exine, and with apertural sites. Multi-membrane bodies are prominent in the cytoplasm, especially subtending aperture sites. Multi-membrane structures continue to be present as pollen wall development proceeds, notably during the early patterning stages. Labelling with the endomembrane-specific fluorochrome DiOC6 does not conclusively lead to membrane identification. However, electron micrographs illustrate elaborate membrane systems during stages when the most obvious developmental activity is initiation of the microspore wall. This suggests that there may be a causal relationship between endomembranes and exine pattern formation.


2005 ◽  
Vol 2005 (265) ◽  
pp. tw13-tw13
Keyword(s):  

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