Functional roles of α 1 -, α 2 -, β 1 -, β 2 -tubulin in vegetative growth, microtubule assembly and sexual reproduction of Fusarium graminearum .

Author(s):  
Yuanye Zhu ◽  
Yuanshuai Zhang ◽  
Yabing Duan ◽  
Dongya Shi ◽  
Yi ping Hou ◽  
...  

The plant pathogen Fusarium graminearum contains two α-tubulin (α 1 and α 2 ) isotypes and two β-tubulin isotypes (β 1 and β 2 ). The functional roles of these tubulins in microtubule assembly are not clear. Previous studies showed that α 1 - and β 2 -tubulin deletion mutants showed severe growth defects and hypersensitivity to carbendazim, which have not been well explained. Here, we investigated the interaction between α- and β-tubulin of F. graminearum . Co-localization experiments demonstrated that β 1 - and β 2 -tubulin are co-localized. Co-immunoprecipitation experiment suggested that β 1 -tubulin binds to both α 1 - and α 2 -tubulin and β 2 -tubulin can also bind to α 1 - or α 2 -tubulin. Interestingly, deletion of α 1 -tubulin increased the interaction between β 2 -tubulin and α 2 -tubulin. Microtubule observation assays showed that deletion of α 1 -tubulin completely disrupted β 1 -tubulin-containing microtubules and significantly decreased β 2 -tubulin-containing microtubules. Deletion of α 2 -, β 1 - or β 2 -tubulin respectively had no obvious effect on the microtubule cytoskeleton. However, microtubules in α 1 - and β 2 -tubulin deletion mutants were easily depolymerized in the presence of carbendazim. The sexual reproduction assay indicates that α 1 - and β 1 -tubulin deletion mutants could not produce asci and ascospores. These results implied that α 1 -tubulin may be essential for the microtubule cytoskeleton. However, our Δα 1 -2×α 2 mutant (α 1 -tubulin deletion mutant containing two copies of α 2 -tubulin) exhibited a normal microtubule network, growth and sexual reproduction. Interestingly, the Δα 1 -2×α 2 mutant was still hypersensitive to carbendazim. In addition, both β 1 -tubulin and β 2 -tubulin were found to bind the mitochondrial outer membrane voltage-dependent anion channel (VDAC), indicating they could regulate the function of VDAC. Importance: In this study, we found that F. graminearum contains four different α-/β-tubulin heterodimers (α 1 -β 1 , α 1 -β 2 , α 2 -β 1 and α 2 -β 2 ) and they assemble together into a single microtubule. Moreover, α 1 -, α 2 -tubulins are functionally interchangeable in microtubule assembly, vegetative growth and sexual reproduction. These results provide more insights into functional roles of different tubulins of F. graminearum which could be helpful for purification of tubulin heterodimers and developing new tubulin-binding agents.

2020 ◽  
Vol 152 (2) ◽  
Author(s):  
María Queralt-Martín ◽  
Lucie Bergdoll ◽  
Oscar Teijido ◽  
Nabill Munshi ◽  
Daniel Jacobs ◽  
...  

Voltage-dependent anion channel (VDAC) is the major pathway for the transport of ions and metabolites across the mitochondrial outer membrane. Among the three known mammalian VDAC isoforms, VDAC3 is the least characterized, but unique functional roles have been proposed in cellular and animal models. Yet, a high-sequence similarity between VDAC1 and VDAC3 is indicative of a similar pore-forming structure. Here, we conclusively show that VDAC3 forms stable, highly conductive voltage-gated channels that, much like VDAC1, are weakly anion selective and facilitate metabolite exchange, but exhibit unique properties when interacting with the cytosolic proteins α-synuclein and tubulin. These two proteins are known to be potent regulators of VDAC1 and induce similar characteristic blockages (on the millisecond time scale) of VDAC3, but with 10- to 100-fold reduced on-rates and altered α-synuclein blocking times, indicative of an isoform-specific function. Through cysteine scanning mutagenesis, we found that VDAC3’s cysteine residues regulate its interaction with α-synuclein, demonstrating VDAC3-unique functional properties and further highlighting a general molecular mechanism for VDAC isoform-specific regulation of mitochondrial bioenergetics.


Cells ◽  
2019 ◽  
Vol 8 (3) ◽  
pp. 239 ◽  
Author(s):  
Marju Puurand ◽  
Kersti Tepp ◽  
Natalja Timohhina ◽  
Jekaterina Aid ◽  
Igor Shevchuk ◽  
...  

In recent decades, there have been several models describing the relationships between the cytoskeleton and the bioenergetic function of the cell. The main player in these models is the voltage-dependent anion channel (VDAC), located in the mitochondrial outer membrane. Most metabolites including respiratory substrates, ADP, and Pi enter mitochondria only through VDAC. At the same time, high-energy phosphates are channeled out and directed to cellular energy transfer networks. Regulation of these energy fluxes is controlled by β-tubulin, bound to VDAC. It is also thought that β-tubulin‒VDAC interaction modulates cellular energy metabolism in cancer, e.g., switching from oxidative phosphorylation to glycolysis. In this review we focus on the described roles of unpolymerized αβ-tubulin heterodimers in regulating VDAC permeability for adenine nucleotides and cellular bioenergetics. We introduce the Mitochondrial Interactosome model and the function of the βII-tubulin subunit in this model in muscle cells and brain synaptosomes, and also consider the role of βIII-tubulin in cancer cells.


2015 ◽  
Vol 83 ◽  
pp. 92-102 ◽  
Author(s):  
Jinjin Wu ◽  
Yuting Liu ◽  
Wuyun Lv ◽  
Xiaofeng Yue ◽  
Yawei Que ◽  
...  

2012 ◽  
Vol 8 (3) ◽  
pp. 446-449 ◽  
Author(s):  
Nadine Flinner ◽  
Enrico Schleiff ◽  
Oliver Mirus

The eukaryotic porin superfamily consists of two families, voltage-dependent anion channel (VDAC) and Tom40, which are both located in the mitochondrial outer membrane. In Trypanosoma brucei , only a single member of the VDAC family has been described. We report the detection of two additional eukaryotic porin-like sequences in T. brucei . By bioinformatic means, we classify both as putative VDAC isoforms.


2014 ◽  
Vol 27 (6) ◽  
pp. 557-566 ◽  
Author(s):  
Shuai Hu ◽  
Xiaoying Zhou ◽  
Xiaoying Gu ◽  
Shulin Cao ◽  
Chengfang Wang ◽  
...  

Like many other filamentous ascomycetes, Fusarium graminearum contains two genes named CPK1 and CPK2 that encode the catalytic subunits of cyclic AMP (cAMP)-dependent protein kinase A (PKA). To determine the role of cAMP signaling in pathogenesis and development in F. graminearum, we functionally characterized these two genes. In addition, we generated and characterized the cpk1 cpk2 double and fac1 adenylate cyclase gene deletion mutants. The cpk1 mutant was significantly reduced in vegetative growth, conidiation, and deoxynivalenol production but it had increased tolerance to elevated temperatures. It was defective in the production of penetration branches on plant surfaces, colonization of wheat rachises, and spreading in flowering wheat heads. Deletion of CPK1 had no effect on perithecium development but the cpk1 mutant was defective in ascospore maturation and releasing. In contrast, the cpk2 mutant had no detectable phenotypes, suggesting that CPK2 contributes minimally to PKA activities in F. graminearum. Nevertheless, the cpk1 cpk2 double mutant had more severe defects in vegetative growth and rarely produced morphologically abnormal conidia. The double mutant, unlike the cpk1 or cpk2 mutant, was nonpathogenic and failed to form perithecia on self-mating plates. Therefore, CPK1 and CPK2 must have overlapping functions in vegetative growth, differentiation, and plant infection in F. graminearum. The fac1 mutant was also nonpathogenic and had growth defects similar to those of the cpk1 cpk2 mutant. However, deletion of FAC1 had no effect on conidium morphology. These results indicated that CPK1 is the major PKA catalytic subunit gene and that the cAMP-PKA pathway plays critical roles in hyphal growth, conidiation, ascosporogenesis, and plant infection in F. graminearum.


2020 ◽  
Vol 5 (1) ◽  
pp. 20-28
Author(s):  
N. A. Davidovich ◽  
O. I. Davidovich

Distribution of diatom algae is limited by their tolerance to environmental factors. Although a genus Toxarium has been evolving for more than 100 million years, it is represented by only two species. Toxarium undulatum is widely spread in tropical and subtropical seas, and it can be also found in the Black Sea, the salinity of which is twice lower than the oceanic one. Ecological and psychological characteristics research of this species is of great interest in terms of its relationship to salinity. T. undulatum clonal cultures were sampled in the Donuzlav Lake connected to the Black Sea (southwest of the Crimean Peninsula) and on Gran Canaria coast (Canary Islands archipelago). Experiments on the salinity tolerance limits showed, that the Black Sea clones were viable in a range of at least 30 ‰ (12 to 42 ‰). The same wide range of salinity tolerance with slightly higher values was observed among oceanic clones of this species. Optima of vegetative growth and sexual reproduction were determined. Optima of the Black Sea clones appeared to be 27.8 and 27.2 ‰, respectively, which was significantly higher than salinity observed in population habitat. Similar higher optima of vegetative growth and sexual reproduction, compared with those salinity values, at which natural population developed, were observed for a number of other Black Sea diatoms, which proved their oceanic (Mediterranean) origin. It was concluded that T. undulatum, along with other species, began to populate the Black Sea basin about seven thousand years ago after Mediterranean Sea water started to flow into the freshened Novoevksinsky Sea-Lake through the Bosporus Strait. However, the evolution rate did not allow bringing physiological and ecological characteristics of the species studied into full agreement with environmental conditions. Oceanic origin is evidently seen in its physiological reactions to salinity. Possibility of speciation due to settlement of the Black Sea with oceanic species is discussed.


PLoS ONE ◽  
2013 ◽  
Vol 8 (6) ◽  
pp. e66980 ◽  
Author(s):  
Qian Zheng ◽  
Rui Hou ◽  
Juanyu ◽  
Zhang ◽  
Jiwen Ma ◽  
...  

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