|
|
|
Search published articles |
|
|
Showing 3 results for Zare
Farshad Fallah, Danial Kahrizi, Abbas Rezaeizad, Alireza Zebarzadi, Lila Zarei, Volume 6, Issue 2 (3-2020)
Abstract
After cereals, oilseeds are the second-largest food reserves in the world. According to available statistics, more than 95 percent of Iran's oil needs are imported. Given the growing need for edible oils in Iran, it is important to identify fatty acids in the oilseed crops. Camelina sativa L. is an oil-medicinal plant and belongs to the Brassicaceae family that requires very little water and fertilizers. It is known as a low input plant. In this study, to analyze the fatty acid profile for breeding programs and specific industries, 137 doubled haploid camelina lines were evaluated in terms of fatty acid composition and variability of fatty acids trait, to estimate phenotypic coefficient of variation (PCV), genotypic coefficient of variation (GCV), heritability, and expected genetic advance. The determination of fatty acid by gas chromatography showed that 18 types of fatty acids were detectable in camelina seed oil. It is shown that the two fatty acids (C14:0 and C16:1) have the highest PCV and GCV. The highest heritability for C20:2, C20:3 and C20:0 fatty acids was estimated 98.92, 98.59 and 96.49 percent, respectively. In this study, two lines with linoleic acid of 35.81-36.67% and four lines with values ranged from 22.08-23.00% were introduced. The ratio of omega-6 to omega-3 (0.479-0.759) was obtained in the studied lines.
Syed Mehran Alavi Mehryan, Nasser Zare, Asad Masumiasl, Parisa Sheikhzadeh, Rasool Asghari, Volume 7, Issue 1 (9-2020)
Abstract
Ferulago angulata (Schlecht) Boiss is one of the valuable and endemic medicinal plants of Iran, which is of great importance due to the source of terpenoid compounds and antimicrobial properties. In current study, the effects of different concentrations of salicylic acid and yeast extract in cell suspension culture of F.angulata on expression pattern of the HMGR and GPPS genes (involved in terpenes biosynthesis) were investigated for the first time. The F. angulata cell suspension cultures were initiated and established using calli derived from leaf explants, and salicylic acid and yeast extract elicitors (with 50, 100 and 150 mg/L concentrations) were added to the cultures during active growth. Then, the cell samples were prepared at 24, 48 and 72 hours after treatment. Analysis of expression pattern of HMGR and GPPS genes using Real-time PCR showed that the expression of both genes were significantly influenced by the type and concentration of the elicitors and also the times after treatment. The relative expression of HMGR and GPPS genes under elicitors were increased compared to the control, and furthermore, the increase in the relative expression of these genes under salicylic acid treatment was significantly higher than that of yeast extract treatment. The highest relative expression of GPPS and HMGR genes was related to 100 mg/L salicylic acid treatment at 24 hours after treatment. However, the highest relative expression of these genes was observed under the 24 and 72 hours after treatment of 150 mg/L yeast extract. The results of this study could be useful in metabolic engineering of F. angulata.
Parastoo Zarei, Hedieh Badakhshan, Ghader Mirzaghaderi, Volume 11, Issue 1 (9-2024)
Abstract
Evaluating genetic diversity in plant species is essential for crop improvement. This research compared the genetic diversity between common oat (Avena sativa) and wild oat (Avena fatua) using molecular markers, phenotypic traits, and chromosomal characteristics. SCoT and IRAP markers generated 283 and 117 bands, respectively. Both marker systems revealed higher polymorphism in wild oat compared to common oat. SCoT markers showed 65.37 percent polymorphism in wild oat versus 60.07 percent in common oat, while IRAP markers exhibited 76.07 and 69.23 percent polymorphism, respectively. Genetic diversity indices (Ne, He, and PIC) indicated slightly higher genetic diversity in wild oat for both marker systems, although the genetic distance between the two species was relatively low. Population structure analysis using Bayesian methods, Principal Coordinate Analysis (PCoA), and Analysis of Molecular Variance (AMOVA) consistently identified distinct subpopulations and significant genetic variation within species. Phenotypic trait analysis revealed significant differences among genotypes. Common oat genotypes generally exhibited greater plant height, while wild oat genotypes had higher 100-seed weight. Heatmap cluster analysis grouped genotypes into three clusters based on phenotypic traits. All genotypes were hexaploid but showed differences in chromosomal parameters such as total chromosome length, centromeric index, and dispersion index. However, no significant differences were found between common and wild oat species in these parameters. Principal Component Analysis (PCA) of chromosomal parameters explained 94.72 percent of the cumulative variance, with PC1 emphasizing centromere position and PC2 highlighting chromosomal asymmetry. This comprehensive study provides valuable insights for breeding and conservation strategies in oat species.
|
|