@article{
 title = {Development and validation of the first SSR markers for Mimosa scabrella Benth},
 type = {article},
 year = {2017},
 identifiers = {[object Object]},
 keywords = {Bracatinga,Next-generation sequencing,NuclearSSR,Polyploidy,Transferability,cpSSR},
 volume = {16},
 websites = {http://www.funpecrp.com.br/gmr/year2017/vol16-1/pdf/gmr-16-01-gmr.16019571.pdf},
 id = {6499e229-2345-3dc3-8b37-6533ca5b57cf},
 created = {2019-02-04T15:29:27.256Z},
 file_attached = {false},
 profile_id = {81a97cb0-31b8-3385-bd0e-efcfffedaada},
 group_id = {b954b4a7-36ce-39f9-9501-2e3795a979e9},
 last_modified = {2019-02-04T15:29:27.256Z},
 read = {false},
 starred = {false},
 authored = {false},
 confirmed = {true},
 hidden = {false},
 citation_key = {Saiki2017},
 source_type = {article},
 notes = {CAPES qualis 2013-2016 CB I: B4},
 private_publication = {false},
 abstract = {© 2017 The Authors. Mimosa scabrella Benth., popularly known as “bracatinga”, is a pioneer and endemic species of Brazil, occurring in Mixed Ombrophilous Forest associated with Brazilian Atlantic Rainforest biomes. It is a fast-growing tree of the Fabaceae family that facilitates the dynamics of ecological succession. SSR development, when there is no genome sequence, is time and labor intensive and there are no molecular markers for M. scabrella. We developed and validated the first microsate llite markers for this tetraploid species, evaluating mother trees and progenies. Using Illumina sequencing, we identified 290 SSR loci and 211 primer pairs. After 31 SSR loci PCR/agarose electrophoresis selection, a subset of 11 primer pairs was synthetized with fluorescence in the forward primer for PCR and capillary electrophoresis validation with leaf DNA of 33 adult and 411 progeny individuals. Polymorphic locus percentage was 36, 4 in 11 loci, 3 chloroplast SSRs, and 1 nuclear SSR. Allele number of polymorphic loci ranged from 2 to 11 alleles considering all sampling. All 11 primer pairs were also tested for cross-species amplification for five FabaceaeMimosoideae species, ranging from 2 loci transferred to Calliandra tweedii Benth. and all 11 loci transferred to Mimosa taimbensis Burkart. The assessed and validated SSR markers for M. scabrella are suitable and useful for analysis and population genetic studies.},
 bibtype = {article},
 author = {Saiki, F. A. and Bernardi, A. P. and Reis, M. S. and Faoro, H. and Souza, E. M. and Pedrosa, F. O. and Mantovani, A. and Guidolin, A. F.},
 journal = {Genetics and Molecular Research},
 number = {1}
}

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Mimosa scabrella Benth., popularly known as “bracatinga”, is a pioneer and endemic species of Brazil, occurring in Mixed Ombrophilous Forest associated with Brazilian Atlantic Rainforest biomes. It is a fast-growing tree of the Fabaceae family that facilitates the dynamics of ecological succession. SSR development, when there is no genome sequence, is time and labor intensive and there are no molecular markers for M. scabrella. We developed and validated the first microsate llite markers for this tetraploid species, evaluating mother trees and progenies. Using Illumina sequencing, we identified 290 SSR loci and 211 primer pairs. After 31 SSR loci PCR/agarose electrophoresis selection, a subset of 11 primer pairs was synthetized with fluorescence in the forward primer for PCR and capillary electrophoresis validation with leaf DNA of 33 adult and 411 progeny individuals. Polymorphic locus percentage was 36, 4 in 11 loci, 3 chloroplast SSRs, and 1 nuclear SSR. Allele number of polymorphic loci ranged from 2 to 11 alleles considering all sampling. All 11 primer pairs were also tested for cross-species amplification for five FabaceaeMimosoideae species, ranging from 2 loci transferred to Calliandra tweedii Benth. and all 11 loci transferred to Mimosa taimbensis Burkart. The assessed and validated SSR markers for M. scabrella are suitable and useful for analysis and population genetic studies.","bibtype":"article","author":"Saiki, F. A. and Bernardi, A. P. and Reis, M. S. and Faoro, H. and Souza, E. M. and Pedrosa, F. O. and Mantovani, A. and Guidolin, A. F.","journal":"Genetics and Molecular Research","number":"1","bibtex":"@article{\n title = {Development and validation of the first SSR markers for Mimosa scabrella Benth},\n type = {article},\n year = {2017},\n identifiers = {[object Object]},\n keywords = {Bracatinga,Next-generation sequencing,NuclearSSR,Polyploidy,Transferability,cpSSR},\n volume = {16},\n websites = {http://www.funpecrp.com.br/gmr/year2017/vol16-1/pdf/gmr-16-01-gmr.16019571.pdf},\n id = {6499e229-2345-3dc3-8b37-6533ca5b57cf},\n created = {2019-02-04T15:29:27.256Z},\n file_attached = {false},\n profile_id = {81a97cb0-31b8-3385-bd0e-efcfffedaada},\n group_id = {b954b4a7-36ce-39f9-9501-2e3795a979e9},\n last_modified = {2019-02-04T15:29:27.256Z},\n read = {false},\n starred = {false},\n authored = {false},\n confirmed = {true},\n hidden = {false},\n citation_key = {Saiki2017},\n source_type = {article},\n notes = {CAPES qualis 2013-2016 CB I: B4},\n private_publication = {false},\n abstract = {© 2017 The Authors. Mimosa scabrella Benth., popularly known as “bracatinga”, is a pioneer and endemic species of Brazil, occurring in Mixed Ombrophilous Forest associated with Brazilian Atlantic Rainforest biomes. It is a fast-growing tree of the Fabaceae family that facilitates the dynamics of ecological succession. SSR development, when there is no genome sequence, is time and labor intensive and there are no molecular markers for M. scabrella. We developed and validated the first microsate llite markers for this tetraploid species, evaluating mother trees and progenies. Using Illumina sequencing, we identified 290 SSR loci and 211 primer pairs. After 31 SSR loci PCR/agarose electrophoresis selection, a subset of 11 primer pairs was synthetized with fluorescence in the forward primer for PCR and capillary electrophoresis validation with leaf DNA of 33 adult and 411 progeny individuals. Polymorphic locus percentage was 36, 4 in 11 loci, 3 chloroplast SSRs, and 1 nuclear SSR. Allele number of polymorphic loci ranged from 2 to 11 alleles considering all sampling. All 11 primer pairs were also tested for cross-species amplification for five FabaceaeMimosoideae species, ranging from 2 loci transferred to Calliandra tweedii Benth. and all 11 loci transferred to Mimosa taimbensis Burkart. The assessed and validated SSR markers for M. scabrella are suitable and useful for analysis and population genetic studies.},\n bibtype = {article},\n author = {Saiki, F. A. and Bernardi, A. P. and Reis, M. S. and Faoro, H. and Souza, E. M. and Pedrosa, F. O. and Mantovani, A. and Guidolin, A. 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