scholarly journals Autophagy Mitigates High-Temperature Injury in Pollen Development of Arabidopsis thaliana

2016 ◽  
Author(s):  
Gonul Dundar ◽  
Zhenhua Shao ◽  
Nahoko Higashitani ◽  
Mami Kikuta ◽  
Masanori Izumi ◽  
...  

AbstractAutophagy is one of the cellular processes that break down cellular components during senescence, starvation, and stress. The susceptibility of plant pollen development to high-temperature (HT) stress is well known, but the involvement of autophagy in HT injury is yet to be clarified. Here, we found that following transfer to 30 °C, all autophagy-deficient (atg) mutants (atg2-1, 5-1, 7-2, and 10-1) of Arabidopsis thaliana tested displayed visibly impaired pollen development and anther dehiscence. HT-induced male sterility significantly increased in the atg mutants, but the degree of HT-induced obstacles did not change between the wild type (WT) and mutants from the seedling stage to the bolting stage. Cytological analyses showed that 30 °C promoted autophagy and autolysosome formation in both anther wall cells and microspores in developing anthers of WT, but the atg5-1 mutant did not show completion of tapetum degeneration and microspore maturation. HT upregulated hydrogen peroxide and dehydroascorbate reductase 1 production in both WT and atg5-1 anthers, but the basal levels were already higher in the mutant. HT repressed expression of UNDEAD and its regulator MYB80, which are required for tapetal programmed cell death (PCD) for proper pollen development. Taken together, our results suggest that autophagy functions in tapetum degeneration and pollen development during HT-caused tapetal PCD abortion.HighlightsIn Arabidopsis, autophagy is not essential for completion of the life cycle under normal temperatures.High temperature (HT) stress induces autophagy in developing anther wall cells and microspores.Autophagy deficient atg mutants become almost completely male-sterile at moderate HT.Autophagy plays a role in tapetum degeneration and pollen development during HT-caused abortion of tapetal program cell death.

1993 ◽  
Vol 71 (4) ◽  
pp. 629-638 ◽  
Author(s):  
J. Dawson ◽  
Z. A. Wilson ◽  
M. G. M. Aarts ◽  
A. F. Braithwaite ◽  
L. G. Briarty ◽  
...  

Five new recessive male-sterile mutants of Arabidopsis thaliana were isolated following seed mutagenesis by X-rays and ethyl methanesulfonate. The cytology of plants homozygous for the msY and msW mutations suggested that pollen development in these lines became abnormal at or before meiosis. The msK mutation caused faulty timing of synthesis or turnover and distribution of callose. In plants homozygous for the msZ mutation, pollen development failed at a late stage. In wild-type plants, the stamen filament elongated just prior to anther dehiscence. In contrast, in the msZ mutant stamen elongation did not occur. Pollen in msH homozygotes was fertile, but anthers failed to dehisce. The msI mutant of J.H. Van der Ween and P. Wirtz (1968. Euphytica 17: 371 – 377) was included in the present study. Pollen development in this mutant failed shortly after microspore release from tetrads. Complementation tests confirmed that the ms mutations were at different loci. Reduced transmission of certain ms genes was observed. Key words: Arabidopsis thaliana, male sterile mutants, anther dehiscence, callose, inheritance.


Planta ◽  
2018 ◽  
Vol 249 (3) ◽  
pp. 913-923 ◽  
Author(s):  
Jacqueline M. Nugent ◽  
Tómas Byrne ◽  
Grace McCormack ◽  
Marc Quiwa ◽  
Elaine Stafford

2019 ◽  
Vol 456 (2) ◽  
pp. 190-200 ◽  
Author(s):  
Gönül Dündar ◽  
Zhenhua Shao ◽  
Nahoko Higashitani ◽  
Mami Kikuta ◽  
Masanori Izumi ◽  
...  

PROTOPLASMA ◽  
2002 ◽  
Vol 219 (1-2) ◽  
pp. 59-71 ◽  
Author(s):  
Chenhong Zhang ◽  
Frédérique C. Guinel ◽  
Barbara A. Moffatt

Author(s):  
M.A. Cuadros ◽  
M.J. Martinez-Guerrero ◽  
A. Rios

In the chick embryo retina (days 3-4 of incubation), coinciding with an increase in cell death, specialized phagocytes characterized by intense acid phosphatase activity have been described. In these preparations, all free cells in the vitreal humor (vitreal cells) were strongly labeled. Conventional TEM and SEM techniques were used to characterize them and attempt to determine their relationship with retinal phagocytes.Two types of vitreal cells were distinguished. The first are located at some distance from the basement membrane of the neuroepithelium, and are rounded, with numerous vacuoles and thin cytoplasmic prolongations. Images of exo- and or endocytosis were frequent; the cells showed a well-developed Golgi apparatus (Fig. 1) In SEM images, the cells was covered with short cellular processes (Fig. 3). Cells lying parallel to or alongside the basement membrane are elongated. The plasma membrane is frequently in intimate contact with the basement membrane. These cells have generally a large cytoplasmic expansion (Fig. 5).


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