Somaclonal variation of haploid in vitro tissue culture obtained from Siberian larch (Larix sibirica Ledeb.) megagametophytes for whole genome de novo sequencing

2014 ◽  
Vol 50 (5) ◽  
pp. 655-664 ◽  
Author(s):  
Konstantin V. Krutovsky ◽  
Iraida N. Tretyakova ◽  
Nataliay V. Oreshkova ◽  
Maria E. Pak ◽  
Olga V. Kvitko ◽  
...  
2017 ◽  
Vol 53 (11) ◽  
pp. 1194-1199 ◽  
Author(s):  
N. V. Oreshkova ◽  
Yu. A. Putintseva ◽  
V. V. Sharov ◽  
D. A. Kuzmin ◽  
K. V. Krutovsky

2021 ◽  
Vol 2 (4) ◽  
pp. 1-8
Author(s):  
Eustache T. A. E. Agbadje ◽  
Arnaud Agbidinoukoun ◽  
Martine Zandjanakou-Tachin ◽  
Gilles T. H. Cacaï ◽  
Corneille Ahanhanzo

Bananas and plantains are among the most important food crops in Central and West Africa. Their plantation is lead to many problems. In the recent decades, biotechnology tools using in vitro culture technics are used for the mass and free disease plantlets production in order to increase the bananas production and the yield. The main way of in vitro tissue culture at this end is the direct organogenesis i.e., the ability of plant tissues to form various organs de novo by shoots or roots induction to differentiate from a cell or cell clusters. This review aims to summarize the main results obtained in the organogenesis of bananas and plantains (Musa spp.) under in vitro conditions and to identify the challenges during the process. The research articles used in this review show that micropropagation is a reliable alternative to conventional production system of bananas and plantains planting material. However, the use of the in vitro micropropagation for bananas and plantains entails choosing the optimal explant type and size according to objectives. Benzylaminopurine remains the preferred cytokinin for in vitro banana and plantain shoot proliferation, while the use of thidiazuron appears to be more and more common. Whichever cytokinin used, the optimal cytokinin concentration for shoot proliferation is genotype dependent. This review also focuses on the causes and control measures of the two major banana and plantain micropropagation constraints: lethal tissues browning/darkening and microbial contaminations. It showed that applying the suitable and available control measure, according to the evolution of culture, is necessary. All this available information on the in vitro conditions makes banana and plantain cultivars in vitro organogenesis possible.


2021 ◽  
Vol 28 (1) ◽  
Author(s):  
Renata Orłowska

Abstract Background Somatic embryogenesis is a phenomenon carried out in an environment that generates abiotic stress. Thus, regenerants may differ from the source of explants at the morphological, genetic, and epigenetic levels. The DNA changes may be the outcome of induction media ingredients (i.e., copper and silver ions) and their concentrations and time of in vitro cultures. Results This study optimised the level of copper and silver ion concentration in culture media parallel with the induction medium longevity step towards obtaining barley regenerants via somatic embryogenesis with a minimum or maximum level of tissue culture-induced differences between the donor plant and its regenerants. The optimisation process is based on tissue culture-induced variation evaluated via the metAFLP approach for regenerants derived under varying in vitro tissue culture conditions and exploited by the Taguchi method. In the optimisation and verification experiments, various copper and silver ion concentrations and the different number of days differentiated the tested trials concerning the tissue culture-induced variation level, DNA demethylation, and de novo methylation, including symmetric (CG, CHG) and asymmetric (CHH) DNA sequence contexts. Verification of optimised conditions towards obtaining regenerants with minimum and maximum variability compared to donor plants proved useful. The main changes that discriminate optimised conditions belonged to DNA demethylation events with particular stress on CHG context. Conclusions The combination of tissue culture-induced variation evaluated for eight experimental trials and implementation of the Taguchi method allowed the optimisation of the in vitro tissue culture conditions towards the minimum and maximum differences between a source of tissue explants (donor plant) and its regenerants from somatic embryos. The tissue culture-induced variation characteristic is mostly affected by demethylation with preferences towards CHG sequence context.


2016 ◽  
Vol 127 (3) ◽  
pp. 543-559 ◽  
Author(s):  
Ileana Gatti ◽  
Fernanda Guindón ◽  
Carolina Bermejo ◽  
Andrea Espósito ◽  
Enrique Cointry

1928 ◽  
Vol 6 (1) ◽  
pp. 1-11
Author(s):  
J. G. H. FREW

In vitro tissue culture Is shown to be a possible mode of experimentation with the tissues of the Blow Fly larva. Methods are described- whereby the tissues, and the body fluids requisite as culture media may be obtained free from bacteria. The imperfections of the technique are noted and the conclusion reached that a successful technique must depend on the rearing of bacteria-free larvae, for which a method Is briefly outlined. It Is shown that progress in this part of the work must await further physiological knowledge, particularly in respect to the nature of the body fluids.


2009 ◽  
Vol 59 (2) ◽  
pp. 179-187 ◽  
Author(s):  
Almudena Montoliu ◽  
María F. López-Climent ◽  
Vicent Arbona ◽  
Rosa M. Pérez-Clemente ◽  
Aurelio Gómez-Cadenas

2015 ◽  
Vol 25 (3) ◽  
pp. 426-434 ◽  
Author(s):  
Brock A. Peters ◽  
Bahram G. Kermani ◽  
Oleg Alferov ◽  
Misha R. Agarwal ◽  
Mark A. McElwain ◽  
...  

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