Sonia Marghali

Genetic diversity in Tunisian perennial ryegrass revealed by ISSR markers

The genetic diversity in Tunisian perennial ryegrass (Lolium perenne) was examined by the help of inter-simple sequence repeats (ISSR). Starting from eighteen accessions, a large number of polymorphic ISSR markers were currently generated using appropriate primers (a total of 136, which average of 12.6 polymorphic bands/primer). These markers were considered to estimate the genetic distance among accessions and to draw phylogenetic trees. Our data provide evidence of a high degree of genetic diversity in Tunisian ryegrass. In addition, both cultivars and wild types present a high degree of divergence suggesting a complex domestication process in this crop. Moreover, spontaneous populations of Tunisian ryegrass have been identified as important ecotypes that are suitable in selection programs to improve grasslands.

Phylogenetic relationships in the North African genus Hedysarum as inferred from ITS sequences of nuclear ribosomal DNA

Sequences of the internal transcribed spacers (ITS) of nuclear ribosomal DNA were analysed to precise their length (637–643 bp) and resolve phylogenetic relationships among eight Mediterranean species of the genus Hedysarum (Fabaceae). The infra-specific variability levels of the ITS sequences of spontaneous population of H. coronarium proved a lack of polymorphism both in the length and in the sequences examined in this species. Hence, a consensus ITS sequence characterising each Hedysarum species has been investigated for analysis of inter-specific polymorphisms. The level of variation of ITS sequence was high enough to make the ITS1 and ITS2 a useful tool for phylogenetic reconstruction. However, ITS2 seems to be relatively more polymorphic and more informative than ITS1 regarding length or GC percent. The phylogenic relationships in the genus Hedysarum based on ITS1 and ITS2 sequences taken independently or together, are discussed in the context of current work in molecular biosystematics. Results exhibited the distinctiveness of the two H. spinosissimum subspecies (i.e. H. spinosissimum ssp. capitatum and H. spinosissimum ssp. spinosissimum). In addition, the great similarity of the ITS sequences between H. coronarium (the only cultivated species of the genus) and H. carnosum suggests the usefulness of the latter in selection programmes to improve pastoral production in semi-arid areas.

Exploration of intra- and inter-population genetic diversity in Hedysarum coronarium L. by AFLP markers

Amplified fragment length polymorphism (AFLP) markers were used to characterize the genetic diversity within and among natural populations and cultivars of Hedysarum coronarium. Twelve populations within Tunisia were evaluated with three AFLP primer combinations. A total of 207 reproducible bands was detected of which 178 (86%) were polymorphic. The great discriminative power of AFLP markers and their ability to represent genetic relationships among Hedysarum plants was demonstrated. Genetic diversity within and among populations was assessed through Principal Component Analysis (PCA) and cluster analysis by using the Neighbor-joining clustering algorithm. AFLP technology has provided evidence of a high degree of intra- and inter-population genetic diversity in H. coronarium. AFLP banding patterns provided molecular markers correlated with the plants’ geotropism. In addition, AFLP markers can differentiate wild accessions from cultivars. Moreover, geographical origins did not correspond to population clustering.

Phylogeny of Mediterranean Lathyrus species using Inter Simple Sequence Repeats markers

Abstract The genus Lathyrus constitutes an important phytogenetic patrimony as a source of traditional foodstuffs in Tunisia. An Inter-Simple Sequence Repeats (ISSR) technique was employed to assess genetic diversity and relationships of seven Mediterranean species of the genus Lathyrus belonging to four sections (Lathyrus, Clymenum, Nissolia and Aphaca). The molecular characterization and fingerprint identification of 11 populations representing the Lathyrus species were conducted using 11 ISSR primers (seven 3’ anchored primers and four non-anchored primers). A total of 261 polymorphic markers have been successfully generated, ranging between 400 and 3000 base pairs, with a mean of 23.72 bands/primer. The percentage of polymorphic bands for these species was 98.12%. The ISSR technique was able to characterize and differentiate between the different studied genotypes of the Lathyrus species. Genetic distance within and between populations was estimated by calculating the similarity index. The similarity indices ranged from 0.251–0.741, with a mean of 0.386. Our data provide evidence of high molecular polymorphism, showing that both wild and cultivated species forms constitute an important pool of diversity. Despite the large distant geographical origin site, the accessions per species issued from different geographical origins are relatively related. Moreover, the genetic similarity tree showed that the two species L. sativus and L. cicera are similar showing that L. sativus may be derived from L. cicera, whereas the principal component analysis showed a clear divergence of the L. ochrus population belonging to section Clymenum from the other populations. Furthermore, L. ochrus appears to be closer to L. aphaca and L. nissolia than to the other studied species belonging to section Lathyrus.

Evaluation of genetic diversity in Sulla coronaria from different geographical populations in Tunisia by inter simple sequence repeat (ISSR)

Five oligonucleotides generating 116 markers complementary to simple sequence repeats were used in order to characterize wild and cultivated ecotypes of Sulla coronaria and assess genetic diversity suitable in breeding programs. While analysing populations, a large genetic variability was revealed and supported by the preferentially allogamous mating system of the species. Moreover, the highest level of intra-population variations (H pop /H sp = 69.9) either of wild or cultivated accessions have been strongly evidenced by a significant adaptation to variety of habitats. In addition, the structure of populations was independent from the bioclimatic stages and was not affected by environmental factors as shown by the non correlation between the geographic and the Nei and Li’s genetic distances (r= 0.461 and p=0.068>0.05). The unweighted pair group method with arithmetic mean (UPGMA) genetic relationships showed that some local spontaneous accessions characterised by an orthotropic port (Jebel Zit and Beja) were also molecularly similar to other cultivars. Key words : Sulla coronaria , wild and cultivated forms, intra and inter-populations variability, microsatellites (ISSRs), bioclimatic stages.

Integrated analysis for identifying Portulaca oleracea and its sub-species based on chloroplastic and nuclear DNA barcoding

Abstract The taxonomy of Portulaca oleracea has been considered as being complex since the aggregate is composed of many subspecies or a group of micro-species based on seed-coat characters, seed size, and chromosome number. In order to enlarge the background of the extent of genetic variability between and within Tunisian P. oleracea accessions, a combined morphological and molecular approach was adapted, in the present survey. The morphological analyses of the spontaneous Tunis population display high intra population variability characterized by two distinct morphotypes corresponding to the botanical forms (wild and cultivated plant). Furthermore, the molecular approach based on sequences data related to chloroplastic and ribosomal DNA, was used to understand this variability. The obtained results highlighted the greater molecular variability of this plant and allowed to segregate between morphotypes and genotypes of Portulaca. Mostly, this work shows the important contribution of DNA barcoding approach in resolving low-level-taxonomy problems to distinguish between natural populations and varieties.

Molecular phylogeny of Lathyrus species: insights from sequence-related amplified polymorphism markers.

Sequence-related amplified polymorphism (SRAP) markers were used to evaluate the intra- and interspecific variation among 40 Lathyrus genotypes (four species) (Fabaceae). Ten SRAP primer combinations resulted in a total of 94 bands, and they exhibited high interspecific variability. The genetic differentiation among Lathyrus, estimated using AMOVA, was highly significant. The results indicated that 58% of the total genetic variation existed among species, and 42% of the differentiation was within species. This was explained by the high level of genome conservation of these species as well as the recent and slow evolution of this genus. These results were confirmed by the topology of the neighbor-joining cladogram and the results of the principal coordinate analysis. Our data support previous results based on seed protein diversity. These results make SRAP markers choice markers for the study of functional polymorphism that is directly related to the transcriptomic data. The SRAP markers used in this study provide an accurate picture of the population structure within Lathyrus germplasm, which is critically important information for the design of genetic diversity and structure analyses. Moreover, further extensive studies are necessary to fully examine other Lathyrus species and tests that adopt the SRAP technique to enrich the Lathyrus library for next-generation sequencing, thus providing a potent protocol for the study of polymorphism.

Sequence divergence of microsatellites for phylogeographic assessment of Moroccan Medicago species

Six Medicago species were investigated to characterize and valorize plant genetic resources of pastoral interest in Morocco. Samples were obtained from the core collection of the South Australian Research and Development Institute (SARDI). The transferability of single sequence repeat markers of Medicago truncatula was successful with 97.6% efficiency across the five species. A total of 283 alleles and 243 genotypes were generated using seven SSR markers, confirming the high level of polymorphism that is characteristic of the Medicago genus, despite a heterozygosity deficit (HO = 0.378; HE = 0.705). In addition, a high level of gene flow was revealed among the species analyzed with significant intra-specific variation. The unweighted pair group method with arithmetic mean dendrogram generated by the dissimilarity matrix revealed that M. polymorpha and M. orbicularis are closely related, and that M. truncatula is likely the ancestral species. The Pearson correlation index revealed no significant correlations between the geographic distribution of the Moroccan species and genetic similarities, indicating local adaptation of these species to different ecological environments independent of their topographical proximities. The substantial genetic variation observed was likely due to the predominance of selfing species, the relative proximity of prospected sites, human impacts, and the nature of the SARDI core collections, which are selected for their high genetic diversity. The results of this first report on Moroccan Medicago species will be of great interest for establishing strategies aiming at reasonable management and selection programs for local and Mediterranean germplasm in the face of increasing environmental change.