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This article is part of the supplement: IUFRO Tree Biotechnology Conference 2011: From Genomes to Integration and Delivery

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Functional markers development and genetic diversity analysis in Eucalyptus globulus with emphasis in wood quality candidate genes

Cintia Acuña*, Pamela Villalba, Martín García, Esteban Hopp and Susana Marcucci

Author Affiliations

Poltri Instituto de Biotecnología, CICVyA, INTA Castelar, CC 25, Castelar (B1712WAA), Argentina

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BMC Proceedings 2011, 5(Suppl 7):P154  doi:10.1186/1753-6561-5-S7-P154

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1753-6561/5/S7/P154


Published:13 September 2011

© 2011 Acuña et al; licensee BioMed Central Ltd.

This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Background

Eucalyptus globulus is the most planted hardwood species for pulpwood in temperate regions. Genomic researches in Eucalyptus have increased the information available in DNA sequences public databases and several structural and regulatory genes involved in the cellulose and lignin pathways are known.

Functional genetic markers, while frequent in crop, are still scarce in forest species. Hence the detection and validation of SSRs in interesting genes to be used in future projects of marker-assisted breeding are needed.

The present study aimed the development of novel functional markers (SSRs) in ESTs and wood quality candidate genes (CG) from Eucalyptus globulus, and analyzes their potential for genetic diversity and individual identification studies.

We report the design of SSR primers flanking simple sequence repeats in ESTs and CG, the validation of a subset of randomly selected EST-SSRs using eight E. globulus genotypes and the screening of a sample of 60 trees with the polymorphic SSRs. Also, SSRs cross-transferability was tested in seven Eucalyptus species coming from three sections: E. grandis, E. saligna (section Latoangulatae); E. globulus, E. dunnii, E. viminalis (section Maidenaria); and E. camaldulensis, E. tereticornis (section Exsertaria).

Material and methods

Plant material

A total of 60 trees, each from a different OP family of E. globulus, were analyzed for their variability. These sixty trees represented major geographical races of the species’ natural distribution that were grown in a field trial in the Province of Buenos Aires, Argentina, between 1995 and 1997. For validation analyses one individual of each race (except Furneaux) was included.

A total of 47 individuals from seven species (including E. globulus) of the genus were sampled for the transferability analyses.

Methods

Novel microsatellites were identified mainly by two different methods:

-SSR Mining software (GDR Server, http://www.rosaceae.org/bio/content?title=&url=/cgi-bin/gdr/gdr_ssr webcite) on selected candidate gene sequences identified at the GenBank.

-SSRs detection from non redundant ESTs of E. globulus from GenBank: Annotations of these SSR-ESTs were based on the Gene Ontology (GO) (http://www.geneontology.org/ webcite) using Blast2GO (http://www.blast2go.org/ webcite) [1].

For validation and diversity analyses, amplification products were silver-stained or analyzed through an ABI3100 Genetic Analyzers (Applied Biosystems, USA) with fluorescent dyes respectively.

SSR statistics for determining number and frequency of alleles, effective number of alleles (Ne), observed heterozygosity (Ho) and unbiased expected heterozygosity estimates (UHe), fixation index (FI) and probability of identity (PI) were determined with the GenAlEx 6.4 program [2]. Tests for Hardy-Weinberg equilibrium were conducted using GENEPOP 4.0.10 [3]. Null allele frequencies were estimated with INEST software (Inbreeding/Null allele estimation) [4], using and Individual Inbreeding Model (IIM) with 10,000 iterations.

Structure analysis was explored through UPGMA and DAS (Shared allele distance) indices as well as Structure [5]software.

Results

From 12,690 updated E. globulus EST database published in National Center for Biotechnology Information a total of 4,924 non-redundant sequences were identified. From these ones, 952 unigenes (19.3%) contained 1,140 SSRs. A new set of 979 primers was designed. The predicted functions of these EST-SSRs were adjudged, including biological process, molecular function and cellular component Gene Ontology (GO) categories.

Twenty four structural and regulatory candidate genes for wood quality carrying 29 SSR were indentified. Microsatellite sequences were located in UTR, introns and exons from candidate genes (CG) from: phenylpropanoid biosynthesis, cellulose biosynthetic process, hemicellulose metabolism, shikimate pathway, methionine metabolism, tubulin genes and the transcriptor factor LIM1.

Sixty five percent out of atotal of 85 SSR (56 EST-SSRs and 29 SSR containg GC) detected in this study were validated for actual PCR amplification of tree DNA samples in eight genotypes of E. globulus. From this assessment a total of 17 polymorphic EST-SSRs and 12 polymorphic CG-SSRs markers were obtained. These ones were selected for further analyses, so as to accurately estimate genetic information content in a larger sample of 60 non related trees represented major geographical races of the species’ natural distribution.

PIC, Ho and UHe values varied over a wide range from around 0.02 to 0.9, whereas the allele number ranged from 2 to 16, with and average of 7.55.

A set of 49 loci (37 validated EST-SSRs (polymorphic and monomorphic) and 12 polymorphic CG-SSRs) were also tested for cross-transferability to other six Eucalyptus species (E. grandis, E. saligna, E. dunnii, E. viminalis, E. camaldulensis, E. tereticornis).A total of 33 out of the 49 validated markers in E. globulus amplified in the six other species and six markers amplified in at least other five.

Finally, the analyses of polymorphism and transferability of functional markers, enabled the selection of a set of 13 (7 EST-SSRs and 6 GC-SSRs) highly informative and transferable to six other species of Eucalyptus.

Conclusions

The set of highly informative markers developed here will have potential use in studies of genetic diversity, taxonomy, gene mapping and will help the improvement of Eucalyptus trough the assisted selection.

Thirty percent of EST-SSRs (17 from 56) are expected to be polymorphic in E. globulus and 25% (14 polymorphic from 56) are expected also to be transferable to other six species (E. grandis,E. saligna, E. dunnii,E. viminalis,E. camaldulensis andE. tereticornis). Under these proportions, potentially more than 200 new EST-SSRs described here may contribute to the verification of synteny and collinearity between different E. globulus maps, and would allow the validation of gene and QTL positions in multiple pedigrees in the botanical sections Maidenaria, Exsertaria, and Latoangulatae, to which most of the commercially planted eucalypt species belong.

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