Showing 2 results for M. Talebi Bedaf
M. Talebi Bedaf, B. E. Sayed-Tabatabaei, K. Razmjoo, B. Shiran,
Volume 10, Issue 2 (summer 2006)
Abstract
Identification of grass species seems difficult due to the morphological similarities. However, selecting desirable parental genotypes of the crosses based on the genetic distances is considered as the most critical step in a breeding program. The aim of this study was to characterize grass species using AFLP techniques. Five species with five cultivars from each were selected and studied using AFLP reactions performed by PstI and MseI restriction enzymes. The obtained data was analyzed using NT SYS-pc Ver. 2.02 software and Jaccard’s method. Ten primer combinations amplified 1170 bands, all of which were polymorphic between cultivars and species. The maximum band (168) and the minimum number of band (81) were produced by P-AAG & M-CAG and P-ACT & M-CGC, respectively. The results also distinguished 5 species in 40% of genetic distances. Some of the markers were special to some special species that can be used in the identification of that species. Additionally, the results showed that AFLP techniques robust and efficient tools for the identification of genetic relationships of different genotypes within species. High levels of bands and polymorphism make AFLP one of the most powerful markers in the determination and classification of species and different cultivars of grass.
M. Bahar, S. Ghobadi, V. Erfani Moghaddam, A. Yamchi, M. Talebi Bedaf, M. M. Kaboli, A. A. Mokhtarzadeh,
Volume 10, Issue 2 (summer 2006)
Abstract
To determine genetic diversity among some Iranian local varieties of alfalfa, six geographically diverse populations including: Bami, Rahnani, Nikshahri, Yazdi, Hamadani (from Isfahan), Hamadani (from Shiraz) along with Ranger, an American commercial variety, were evaluated using a set of 24 EST-SSR primers developed from cDNA library of Medicago truncatula and three microsatellite loci, identified from genomic library of M. sativa. Of the pairs of primers tested, four loci from EST-SSRs (AW9, BEE, TC6 and TC7) and genomic microsatellite (Afctt32), were found appropriate for assessing genetic diversity between these alfalfa genotypes. In total, 46 alleles were detected from the five loci in the samples of alfalfa examined. The number of alleles per locus in populations ranged from six to eleven and genetic diversity indices of loci were variable from 0.62 to 0.87 for the populations. Genetic relationship analysis of EST-SSR data revealed separation of Iranian populations from Ranger. It is likely that the parental origin of primary population from which Ranger has been derived is different from that of Iranian populations. Iranian local populations of alfalfa in this study were grouped in two main clusters. Alfalfa populations Hamadani and Rahnani, which are adapted to cold claimates, were grouped in one cluster and populations Bami, Yazdi and Nikshahri, belonging to the trpoical areas, were placed in the next cluster. The positioning of EST-SSR loci in coding regions of genome, possibly increases the usefulness of these markers to clarify inter specific genetic relationships among alfalfa populations.
