جستجوی مقالات مرتبط با کلیدواژه "جنین" در نشریات گروه "زراعت"

Rice (Oryza sativa L.) feeds more than half of the world's population. Rice is considered a model plant in biological and agriculture field research due to its small genome compared with other plants. Storage proteins in the aleurone layer of rice seeds include albumin and globulin, as well as the endosperm, prolamin, and glutelin proteins. To determine the number of proteins and identify the protein spots between the tissues of two embryo samples and rice endosperm, the protein spots were matched according to their expression level in the images obtained from two-dimensional gel electrophoresis.
The profile of proteins in the endosperm and embryo of rice seeds was determined using isoelectric focusing (IEF) and polyacrylamide gel electrophoresis(SDS-PAGE) methods. The Image Master software was utilized to analyze the two-dimensional gels. Considering the importance of local rice consumption in Iran and the significant production of this economically important crop in the country, this study aimed to determine the diversity and differences in the expression of protein spots within the linear pH range of 4 to 7. The two-dimensional electrophoresis method was employed on the Hasan-Sarai variety of rice indigenous to the region of Guilan. For this research, the cultivar being examined was procured from the Guilan Rice Research Center. Subsequent stages of the experiment, including sample separation and total protein extraction, were conducted at the Payame Noor University laboratory in Asadabad. Ultimately, the protein samples obtained were sent to the Health Research Institute at the Faculty of Pharmacy, where two-dimensional electrophoresis was carried out using an isoelectric focusing device. Finally, the extracted protein samples were transferred to the Health Research Institute of the Faculty of Pharmacy to perform two-dimensional electrophoresis using an isoelectric focusing device.
Based on the results of the two-dimensional gel analysis, a large part of the protein spots are present in the pH range of 4 to 7. The analysis of protein profile based on standard proteins with specific molecular weight and isoelectric point indicates that embryo tissue and endosperm based on isoelectric point and molecular weight showed that 284 protein spots in the embryo and 123 protein spots in endosperm have been identified. Among the identified spots, 57 common protein spots showed increased and decreased expression between the two samples. The presence of remaining protein spots in the two samples showed a significant difference between protein content in the embryo and endosperm.
Image master software was used to determine the isoelectric point and molecular weight of protein spots and expression changes between common spots. Analysis was done in protein databases and possible proteins were identified in embryo tissue and endosperm. The proteins identified in rice endosperm and embryo tissue in two-dimensional electrophoresis included grain storage proteins, glutelin precursors, acidic and alkaline glutelins, globulins, prolamins, HSPs, and hypothetical proteins. Therefore, in this way, it is possible to identify the level of expression of proteins and also their biosynthetic pathways.

Production of pure lines is one of the most important tools due to production of high-yield seeds. Pure lines can be produced in a short time using in vitro techniques and therefore, reduce several years in required time for conventional plant breeding programs. The purpose of this study was investigation of different concentrations of TDZ on production of haploid plants in cucumber ovule culture. The experimental layout was conducted in factorial arrangement in randomized complete design with three replications in greenhouse and laboratory of Razi university during 2015-2017. Factors were two cucumber genotypes (Esfahani and Beit Alfa) and different concentrations of TDZ (0, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08 mg/l). Unfertilized ovaries were harvested 1 day before an thesis and they were sliced into 1 mm cross sections under sterile conditions and placed on solid MS medium. Immediately after placing the unfertilized ovary slices of each genotype on induction medium, they were exposed to a thermal shock pretreatment at 35±1°C for 3 days. The first visual structures formed after 3 days in culture. After two weeks of culture, the frequency of embryo formation was recorded. After embryogenesis, the embryos were sub-cultured in medium containing 1.5 mg/L-1 GA3 and finally cultured in medium containing 0.05 mg/L-1 NAA and 1.5 mg/L-1 BAP for organogenesis. Results indicated a statistically significant effect at 1% among TDZ concentrations. Genotypes and interaction between genotype and TDZ concentration did not have a significant effect on embryo induction. According to the results of means comparison, M8 medium with the average of 23.33 for Esfahani genotype and 20.66 for Beta Alfa genotype had the highest embryo induction and M1 showed the lowest embryo induction for both genotypes. Ploidy level of calli and embryos were identified by Flucytometry assay. Haploid embryos were transferred to the regenerative medium. The chromosome content of haploid plants was doubled spontaneously in all regenerated plants. Double haploid plants originated from megaspore and they were equivalent to haploid, which relates to homozygosity and can be used directly in breeding program. The high number of embryos was obtained in high concentration of TDZ (0.08 mg/l). Flucytometry assay is a way to recognizing ploidy level in plant tissues; thus it could be useful in choosing haploid tissue. Spontaneous chromosome doubling may occur via somatic cell fusion, endoreduplication, endomitosis and possibly many other mechanisms. In conclusion, the higher rates of embryo formation frequency achieved and doubled haploids obtained in the present study are promising for future work.

In order to use of haploid tissue of sugar beet for producing transgenic plants, at first, some experiments were accomplished for shoot production of haploid leaves from haploid embryos. Results of current study indicated that MSB or PGoB medium supplemented with 3% sucrose, 0.2 mgl-1 BA and 0.5 mgl-1 NAA could be used for increasing haploid embryos and half strength MSB medium contains 1% sucrose to develop embryos and shoot production. Moreover, PGoB medium supplemented with 1 mgl-1 BA and 1 mgl-1 NAA was used for shoot production from haploid leaves. In the next step, haploid embryogenic calli and leaves were inoculated with Agrobacterium tumefaciens cells harboring pBI121 binary vector. After 2 days co-culture, the inoculated explants were transferred to selection medium contains 50 mgl-1 kanamycin. After 3-5 weeks, putative transgenic shoots were analyzed by GUS staining. Results showed that two explants have ability for shoot regeneration of haploid transgenic cells.