Development of microsatellite molecular markers and genetic diversity in Hevea Braziliensis

Abstract

Background The rubber tree [Hevea Braziliensis (Willd. ex Adr. De Juss.) Muell-Arg.] is native from the Amazon region which has great economic importance for being the largest source of natural rubber in the world. Although Brazil is the center of origin and genetic diversity of this culture, the country is currently responsible for only 1% of the world production. Besides offering optimal weather conditions for crop development, the Amazon rainforest region is also favorable to the development of the fungus known as SALB (South American leaf blight), which causes the disease-of-leaves. Leaves fall sharply reducing the production of latex, limiting the production of rubber in this region. Thus breeding programs are seeking for clones which are resistant to this fungus and with high production in escape regions, which provide stress conditions such as low temperatures, high altitude, wind and other diseases [1]. The rubber tree is perennial and requires about 30 years to obtain an improved variety, starting from the controlled pollination of a clone to the final recommendation. Molecular markers such as microsatellites (Simple Sequence Repeats, SSRs) are an important tool for diversity studies and potentially to assist breeding programs. This study aimed to develop an enriched microsatellite library for H. Braziliensis, characterize these developed microsatellite markers and test the transferability of these markers to six other species of the genus Hevea. Material and methods For this study we used 36 accessions of H. Braziliensis donated by the Agronomy Institute of Campinas and one accession of each of six other species of genus Hevea (H. nitida, H.pauciflora (2), H.camargoana, H.guianensis, H. rigidifolia andH. benthamiana) provided by Embrapa. Genomic DNA samples were extracted from lyophilized leaf tissues using a modified CTAB method [2]. Trinucleotide and dinucleotide enriched genomic libraries for H. Braziliensis were constructed. The DNA samples were digested with AFAI and enriched using (CT)8 and (GT)8 biotinylated microsatellite probes for the dinucleotide library and (ATC)8 and (CCT)8 for the trinucleotide library. The clones obtained were sequenced and the sequences were evaluated with the Microsat program, which removes parts of the vector and the adapters and verifies the presence of restriction site within the sequence. After this step, the sequences were aligned and edited using the program SeqMan (DNAStar Inc.), which also allows analyzing the redundancy of the library. The identification of microsatellites was performed using a research tool SSRs SSRIT – “The Simple Sequence Repeat Identification Tool” avaiable at Gramene [http:// www.gramene.org]and primers complementary to sequences flaking the microsatellites were designed by Primer Select Program (DNAStar Inc) and Primer 3. Amplification tests were made from a temperature gradient to know the annealing temperature and the products were evaluated and resolved on 3% agarose gels stained with ethidium bromide and in denaturing 6% polyacrylamide and silver stained [3]. The loci were characterized on the number of alleles per locus, allele frequency and the Polymorph Information Content (PIC). It was also made analysis of ancestry for de accessions of H. Braziliensis using the program Structure v 2.3.3 [4]. * Correspondence: camila.mantello@gmail.com Molecular Genetic Analysis Laboratory Molecular Biology Center and Genetic Engineering (CBMEG), UNICAMP, Campinas, Sao Paulo, 13083-875, Brazil Full list of author information is available at the end of the article Mantello et al. BMC Proceedings 2011, 5(Suppl 7):P11 http://www.biomedcentral.com/1753-6561/5/S7/P11