Some influence of the hormonal components in nutrient medium onthe induction of novel structures when obtaining rapeseed haploids through in vitro culture

Growth regulators, phytohormones, both natural and artificial, are the main means to control plant ontogenesis. They are involved in regulating the processes of cell differentiation and cell divisions, the formation of tissues and organs, the changes in the rate of growth and development, the duration of the certain stages of ontogenesis. The main classes of phytohormones used in plant biotechnology, in particular, in the induction of haploid structures, are auxins and cytokinins. The mechanism of action of phytohormones on a cell is rather complicated and may have a different character. Understanding the characteristics of the action of phytohormones is complicated by the fact that the system of hormonal regulation of plant life is multicomponent. This is manifested in the fact that the same physiological process is most often influenced not by one, but by several phytohormones, covering a wide range of aspects of cell metabolism. In connection with the foregoing, the purpose of our work was to test a set of nutrient media with different basic composition and different proportions of phytohormones to determine the patterns of their influence on the processes of haploid structure induction in rape anther culture using accessions, developed at the Institute of Oilseed Crops NAAS. The material used was two accessions of winter rapeseed (No. 1 and No. 2) and one sample of spring rapeseed, provided by the Rapeseed Breeding laboratory of the Institute of Oilseed Crops. Incised inflorescences were kept against the background of low temperature of 6–8 ° C for several days, and then, under aseptic conditions, anthers with unripe pollen grains were isolated and planted on nutrient media differing in both basic mineral composition and content of phytohormones. MS (Murashige & Skoog 1962) and B5 (Gamborg et al 1968) media were used as basic media. Phytohormones were added to the basic media in various combinations – BA, 2,4-D, NAA at the concentrations of 0.1-0.6 mg/l. In each treatment up to 300 anthers were cultivated. Differences between treatments were evaluated using standard t-test. Studies have shown that in the anther culture of rapeseed on the tested nutrient media, morphogenic structures of different types (embryoids and callus) were originated. Synthetic auxin 2,4-D, regardless of the composition of the basic medium, caused the formation of structures of both types, though with a low frequency. Phytohormone BA of the cytokinin type had a similar effect. In this case, the frequency of structures was slightly higher, and the developed structures were represented mainly by embryoids. The joint action of cytokinin and auxin was the most favorable for the initiation of morphogenic structures. Such combination of phytohormones caused the formation of these structures with a frequency of 24.5-14.7% in the studied genotypes of winter rape. A similar effect of phytohormones on the induction and development of morphogenic structures was also observed in spring rape. In this case, a single basic MS medium was used. The experiment included treatments where phytohormones were absent (control), as well as various combinations of auxin and cytokinin. In the control treatment, the formation of new structures was not noted. In treatments with phytohormones, in addition to the medium with the combination of auxin and cytokinin, the medium in which only cytokinin was present was also rather effective. The treatment in which the action of auxin 2,4-D was combined with the action of another auxin, NAA, turned out to be practically ineffective. Thus, it was found that for the induction of morphogenic structures from microspores in rape anther culture of the tested genotypes, the combination of cytokinin with auxin, or the use of only single cytokinin BA without other phytohormones, had the most positive effect.

1999 ◽  
Vol 9 (4) ◽  
pp. 585-588 ◽  
Author(s):  
Richard E. Veilleux

Anther culture has been one of the most successful techniques for generating haploid plants over a wide range of species. It is a reasonably simple procedure that can be accomplished successfully without sophisticated laboratory facilities; yet, the plants generated through anther culture can be used to demonstrate the application of many modern methods that have direct applicability to plant breeding. Anthers of diploid potato clones that have been selected for competence in anther culture can be cultured in a simple medium to yield androgenic embryos after 5 weeks. Plant regeneration requires an additional 3 to 4 weeks. Regenerated plants should be large enough 2 weeks after transfer to basal medium for ploidy determination by any of three methods depending on available facilities: chromosome counts in root tips; chloroplast counts in stomatal guard cells; or flow cytometry of nuclei released from in vitro plantlets. DNA can be extracted from anther-derived plantlets using a rapid extraction procedure to demonstrate segregation of PCR (polymerase chain reaction)-based markers such as RAPD (randomly amplified polymorphic DNA), RAMPs (randomly amplified microsatellite polymorphisms), or microsatellites. Microsatellite markers that were heterozygous in the anther donor can be used to verify haploidy in anther-derived plants. If an anther culture laboratory is scheduled early in a semester, such molecular analysis can be planned for late in the same semester.


Author(s):  
E. A. de T. Picoli ◽  
P. R. Cecon ◽  
M. G. Fári ◽  
W. C. Otoni

The influence of antibiotics (cefotaxime, timentin, kanamycin and hygromycin) and growth regulators (indolacetic acid and 6-benzylaminopurine) was evaluated on eggplant organogenesis. Solanum melongena hypocotyl segments (6 to 10 mm length), taken from 16 to 20-days in vitro grown seedlings, were used as explants. The basic medium was composed by MS salts, Gamborg vitamins and 2% sucrose, solidified with agar 0.8% and pH adjusted to 5.7±0.2. Morphogenesis was impaired at 50 to 100 mg L-I kanamycin and 7.5 mg L-1 hygromycin. Both Timentin and cefotaxime reduced the frequency of regenerating explants meanwhile hyperhydricity was not affected. A decrease in root regeneration was observed with increasing cefotaxime concentrations, although, timentin had no effect on root regeneration, as compared to the control treatment. Interestingly, the number of adventitious roots was more noticeable at 0.25 mg L-I IAA plus 0.5 mg L-1 BAP. However, if just IAA was added led to higher number of regenerated roots compared to other treatments.


Genome ◽  
1989 ◽  
Vol 32 (1) ◽  
pp. 54-56 ◽  
Author(s):  
J. De Buyser ◽  
B. Bachelier ◽  
Y. Henry

Gametic selection was investigated in a monosomic 1D line of wheat. Comparison of chromosome numbers in progenies from cross- or self-pollination and anther culture indicated the frequency of the different types of gametes acting in zygote formation. The progenies obtained from reciprocal crosses (monosomic × euploid) were different in terms of frequencies of monosomic plants. All the pollen grains do not have an equal probability of fertilization since a strong gametic selection for euhaploid male gametes was observed when the monosomic line was used as male parent; only 13% of the nullisomic survived to embryogenesis and seed germination. Regenerants from anther culture also demonstrated that the percentage of nullihaploids was reduced, indicating a strong selection for euhaploid gametes. A comparison between the frequency of male nullihaploid gametes in the cross disomic × monosomic and in the anther culture revealed that the two processes generate the same gamete transmission. The in vitro cultures do not induce more selection pressure than the embryogenic development even if they are together biased samples of the male gametic population.


1985 ◽  
Vol 27 (6) ◽  
pp. 759-765 ◽  
Author(s):  
J. Rueda ◽  
A. M. Vázquez

Anthers of rye excised at premeiotic interphase were cultured in vitro on a basic medium and on a series of auxin- and cytokinin-containing media to ascertain the effect of these plant hormones upon the start of meiosis. Only in the hormone-containing media was it possible to find anthers in which pollen mother cells had started the meiotic division. The different hormones and concentrations tested exhibited a differential capacity to induce the start of meiosis, the percentages of anthers with pollen mother cells in meiosis varying from 0% in one medium to more than 60% in two other media. In some media, pollen mother cells were able to complete the whole meiotic division, while in others they were arrested at different stages of meiosis.Key words: Secale cereale, meiosis induction, anther culture, plant hormones.


Genetika ◽  
2017 ◽  
Vol 49 (1) ◽  
pp. 105-115 ◽  
Author(s):  
Dusica Calic ◽  
Ljiljana Radojevic

Pollen quality of horse chestnut, expressed as pollen productivity, viability and germination was studied. Anthers of horse chestnut genotypes had pollen production from 3.66 to 5.06 x 103 pollen grains per anther, depending of genotype. Also, pollen of horse chestnut Ah1-Ah4 genotypes showed different viability (from 56 to 68%), after staining with fluorescein diacetate. Pollen germination of Ah1-Ah4 genotypes varied from 50-66% on basic medium. Inclusion of polyethylene glycol-PEG from 10%, 15% and 20% v/w increased pollen germination. The best results were achieved on medium with the largest PEG concentration. On these medium 76-91% pollen grains were germinated, depending of genotype. The best pollen quality, for all tested parameters, had genotype Ah2. Knowledge about morphology, production, viability, in vitro germination, tube growth as well as pollen: ovule ratio can be of great importance for future pollen biology studies.


2000 ◽  
Vol 30 (2) ◽  
pp. 329-332 ◽  
Author(s):  
Nicole Dumont-BéBoux ◽  
Bradley R Anholt ◽  
Patrick von Aderkas

We have been able to successfully germinate western larch (Larix occidentalis Nutt.) pollen in vitro. Pollen was rehydrated at 100% RH for 16 h before being sprinkled on semisolid and liquid media. The basic medium contained Brewbaker and Kwack minerals diluted 1:10 and was supplemented with polyethylene glycol 4000 and three different concentrations of sucrose. The flavonol quercetin was also included in half of the media. More pollen grains survived on liquid media, but semisolid media gave superior germination results. Two to 9% of the grains produced tubes. Quercetin had no major effect on germination, viability, or tube length.


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