Creation of hybrid vigor through nuclear transplantation in Phytophthora

2001 ◽  
Vol 47 (7) ◽  
pp. 662-666 ◽  
Author(s):  
Yu-Huan Gu ◽  
Wen-Hsiung Ko
Keyword(s):  
Protoplast Fusion ◽  
Fungicide Resistance ◽  
Phytophthora Capsici ◽  
Hybrid Vigor ◽  
Nuclear Transplantation ◽  
Phytophthora Parasitica ◽  
Isolated Nuclei ◽  
Donor Cells ◽  
Potential Applications ◽  
Fusion Products

When isolated nuclei of a diploid oomycete, Phytophthora parasitica, were fused with protoplasts of another strain of the same species, the regenerated nuclear hybrids grew faster than the parental isolates. Such a phenomenon did not occur in hybrids regenerated from mitochondrion–protoplast or protoplast–protoplast fusion products between these two strains. These results indicate that hybrid vigor is the result of the interaction between two different kinds of nuclei, but not between mitochondria, and they suggest that the presence of mitochondria from nuclear donor cells represses the expression of increased vigor. The nuclear hybrids also expressed increased fungicide resistance and propagule production. Increased vigor in growth was also observed in the interspecific nuclear hybrids when isolated nuclei of P. parasitica were transferred into protoplasts of Phytophthora capsici, and vice versa. This phenomenon may have potential applications, such as the creation of superior fungal strains and plant cultivars with improved commercial traits for usage in industry and agriculture.Key words: hybrid vigor, nuclear transplantation, Phytophthora parasitica, Phytophthora capsici.

Evidence for mitochondrial gene control of mating types in Phytophthora

2005 ◽  
Vol 51 (11) ◽  
pp. 934-940 ◽  
Author(s):  
Yu-Huan Gu ◽  
Wen-Hsiung Ko
Keyword(s):  
Mating Type ◽  
Mitochondrial Gene ◽  
Phytophthora Capsici ◽  
Nuclear Genes ◽  
Gene Control ◽  
Mating Types ◽  
Phytophthora Parasitica ◽  
Decisive Effect ◽  
Mating Type Genes ◽  
Fusion Products

When protoplasts carrying metalaxyl-resistant (Mr) nuclei from the A1 isolate of Phytophthora parasitica were fused with protoplasts carrying chloroneb-resistant (Cnr) nuclei from the A2 isolate of the same species, fusion products carrying Mr nuclei were either the A2 or A1A2 type, while those carrying Cnr nuclei were the A1, A2, or A1A2 type. Fusion products carrying Mr and Cnr nuclei also behaved as the A1, A2, or A1A2 type. The result refutes the hypothesis that mating types in Phytophthora are controlled by nuclear genes. When nuclei from the A1 isolate of P. parasitica were fused with protoplasts from the A2 isolate of the same species and vice versa, all of the nuclear hybrids expressed the mating type characteristics of the protoplast parent. The same was true when the nuclei from the A1 isolate of P. parasitica were fused with the protoplasts from the A0 isolate of Phytophthora capsici and vice versa. These results confirm the observation that mating type genes are not located in the nuclei and suggest the presence of mating type genes in the cytoplasms of the recipient protoplasts. When mitochondria from the A1 isolate of P. parasitica were fused with protoplasts from the A2 isolate of the same species, the mating type of three out of five regenerated protoplasts was changed to the A1 type. The result demonstrated the decisive effect of mitochondrial donor sexuality on mating type characteristics of mitochondrial hybrids and suggested the presence of mating type genes in mitochondria. All of the mitochondrial hybrids resulting from the transfer of mitochondria from the A0 isolate of P. capsici into protoplasts from the A1 isolate of P. parasitica were all of the A0 type. The result supports the hypothesis of the presence of mating type genes in mitochondria in Phytophthora.Key words: mating type, mitochondrial gene, Phytophthora parasitica, Phytophthora capsici.

Transplantation and subsequent behavior of mitochondria in cells of Phytophthora

2000 ◽  
Vol 46 (11) ◽  
pp. 992-997 ◽  
Author(s):  
Y H Gu ◽  
W H Ko
Keyword(s):  
Antibiotic Resistance ◽  
Asexual Reproduction ◽  
Second Generation ◽  
Random Distribution ◽  
Phytophthora Capsici ◽  
Selective Medium ◽  
Phytophthora Parasitica ◽  
Subsequent Behavior ◽  
Hybrid Antibiotic ◽  
Fusion Products

Mitochondria isolated from streptomycin-resistant (Sr) protoplasts of Phytophthora parasitica were transferred into chloramphenicol-resistant (Cpr) protoplasts of P. parasitica or Phytophthora capsici with an average successful rate of 1.7 × 10-4, using a selective medium containing streptomycin. No colonies appeared when self-fusion products of donor mitochondria or recipient protoplasts were exposed to the selective medium. Mitochondria isolated from Cpr protoplasts of P. capsici were also transferred into Sr protoplasts of P. parasitica with a similar success rate using a selective medium containing chloramphenicol. Zoospores produced by the Cpr+Sr intraspecific mitochondrial hybrid gave rise to Sr and Cpr+Sr cultures. The second generation zoospores produced by Sr and Cpr+Sr cultures also gave rise to Sr and Cpr+Sr cultures, suggesting the possible occurrence of fusion between some of the Cpr mitochondria and Sr mitochondria, and the displacement of non-fused Cpr mitochondria in the receptor protoplast by the donor Sr mitochondria. Zoospores produced by the interspecific mitochondrial hybrid gave rise to Cpr, Sr, Cpr+Sr, and Cps +Ss cultures. The second generation zoospores produced by Cpr+Sr or Sr cultures also gave rise to the same four types of cultures, suggesting the existence of residual antibiotic-sensitive mitochondria (Cps+Ss) in the parental isolates and the random distribution of Cpr, Sr, and Cps+Ss mitochondria during asexual reproduction. Results suggest that the phenotype of antibiotic resistance / sensitivity was the end result of the interactions among the three types of mitochondria.Key words: mitochondrial transplantation, mitochondrial hybrid, antibiotic resistance, Phytophthora parasitica, Phytophthora capsici.

Segregation following interspecific transfer of isolated nuclei between Phytophthora parasitica and P. capsici

2000 ◽  
Vol 46 (5) ◽  
pp. 410-416 ◽  
Author(s):  
Y H Gu ◽  
W H Ko
Keyword(s):  
Nuclear Transfer ◽  
Phytophthora Capsici ◽  
Selective Medium ◽  
Crossing Over ◽  
Phytophthora Parasitica ◽  
Parasexual Cycle ◽  
Different Types ◽  
Average Success Rate ◽  
Fusion Products ◽  
Interspecific Transfer

Nuclei isolated from metalaxyl-resistant (MR) protoplasts of Phytophthora parasitica were transferred into chloroneb-resistant (CnR) protoplasts of Phytophthora capsici and vice versa, with an average success rate of 2.6 × 10-4 (protoplasts with donor nuclei/regenerated protoplasts), using a selective medium containing only the fungicide tolerated by the nuclear donor. No colonies appeared when self-fusion products of donor nuclei or recipient protoplasts were exposed to the selective medium. Colonies produced by the nuclear transfer formed sectors commonly, and differed from the parental types in appearance. All the zoospores produced by the nuclear hybrids were of normal size, and one-fifth of them contained both MR and CnR genes. Since zoospores are mostly uninucleate, these results indicated the occurrence of chromosome re-assortment or mitotic crossing-over following the production of transitory tetraploids, followed by diploidization during zoosporogenesis, thus suggesting the completion of events leading to a parasexual cycle. Hyphal fragment cultures from a nuclear hybrid tested showed considerable variation in growth rate, mycelial morphology, and level of resistance to metalaxyl, indicating uneven distribution and continuous segregation of different types of nuclei in mycelia during vegetative growth.Key words: interspecific nuclear transfer, parasexual cycle, karyogamy, Phytophthora parasitica,Phytophthora capsici.

scholarly journals Extracellular Vesicles: Novel Opportunities to Understand and Detect Neoplastic Diseases

2021 ◽  
pp. 030098582199932
Author(s):  
Laura Bongiovanni ◽  
Anneloes Andriessen ◽  
Marca H. M. Wauben ◽  
Esther N. M. Nolte-’t Hoen ◽  
Alain de Bruin
Keyword(s):  
Extracellular Vesicles ◽  
Biologically Active ◽  
Liquid Biopsies ◽  
Donor Cells ◽  
Recent Developments ◽  
Veterinary Pathology ◽  
Cell Components ◽  
Potential Applications ◽  
Intercellular Communications

With a size range from 30 to 1000 nm, extracellular vesicles (EVs) are one of the smallest cell components able to transport biologically active molecules. They mediate intercellular communications and play a fundamental role in the maintenance of tissue homeostasis and pathogenesis in several types of diseases. In particular, EVs actively contribute to cancer initiation and progression, and there is emerging understanding of their role in creation of the metastatic niche. This fact underlies the recent exponential growth in EV research, which has improved our understanding of their specific roles in disease and their potential applications in diagnosis and therapy. EVs and their biomolecular cargo reflect the state of the diseased donor cells, and can be detected in body fluids and exploited as biomarkers in cancer and other diseases. Relatively few studies have been published on EVs in the veterinary field. This review provides an overview of the features and biology of EVs as well as recent developments in EV research including techniques for isolation and analysis, and will address the way in which the EVs released by diseased tissues can be studied and exploited in the field of veterinary pathology. Uniquely, this review emphasizes the important contribution that pathologists can make to the field of EV research: pathologists can help EV scientists in studying and confirming the role of EVs and their molecular cargo in diseased tissues and as biomarkers in liquid biopsies.

Commercial applications of nuclear transfer cloning: three examples

2005 ◽  
Vol 17 (2) ◽  
pp. 59 ◽  
Author(s):  
Erik J. Forsberg
Keyword(s):  
Nuclear Transfer ◽  
Social Acceptance ◽  
Polyclonal Antibodies ◽  
Genetically Modified ◽  
Single Sex ◽  
Genetic Modifications ◽  
Donor Cells ◽  
Potential Applications ◽  
Commercial Applications ◽  
Made In

Potential applications of cloning go well beyond the popularly envisioned replication of valuable animals. This is because targeted genetic modifications can be made in donor cells before nuclear transfer. Applications that are currently being pursued include therapeutic protein production in the milk and blood of transgenic cloned animals, the use of cells, tissues and organs from gene-modified animals for transplantation into humans and genetically modified livestock that produce healthier and safer products in an environmentally friendly manner. Commercial and social acceptance of one or more of these early cloning applications will lead to yet unimagined applications of nuclear transfer technology. The present paper summarises progress on three additional applications of nuclear transfer, namely the development of male livestock that produce single-sex sperm, the transfer of immune responses from animals to their clones to permit the production of unlimited supplies of unique polyclonal antibodies, and the generation of genetically modified animals that accurately mimic human diseases for the purpose of developing new therapies. However, the myriad applications of cloning will require appropriate safeguards to ensure safe, humane and responsible outcomes of the technology.

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