DEVELOPMENT OF A DArT
MICROARRAY FOR COMPARATIVE STRUCTURAL GENOMICS AND MAPPING OF AGRICULTURALLY
SIGNIFICANT GENES IN WILD POTATO SPECIES
M. IORIZZO1, J. M. BRADEEN2,
L. FRUSCIANTE1, D. CARPUTO1
1 Department of Soil, Plant and
Environmental and Animal Production Sciences, , School of Biotechnology, University of Naples ÒFederico IIÓ (ITALY)
2 Department of Plant Pathology,
University of Minnesota (MN, USA)
Efficient access to genetic variability is important
for breeding programs. For potato improvement, the approximately 180 wild
species represent a valuable source for agriculturally significant genes,
including genes for disease resistance and cold tolerance. We specialize in a group of 20 wild
potato species that collectively comprise the tertiary genepool for cultivated
potato. These species are sexually
incompatible with cultivated potato, but genes from these species can be
accessed using bridge crosses, somatic hybridization, and gene cloning and
transformation. To improve access
to agriculturally significant genes from tertiary genepool species, we have
initiated an effort of comparative structural genomics using the Diversity
Array Technology (DArT) marker platform. The first phase of this
project was development of the DArT microarray. We used five diverse tertiary
genepool species for array construction: Solanum commersonii, S.
bulbocastanum, S. polyadenium, S. chacoense, and S. pinnatisectum. Six accessions for each species were
included. Now, DArT array validation via phylogenetic comparison is
ongoing. In this phase of our
study, deduced relationships between the five species used in array
construction plus S. circaeifolium and S. cardiophyllum will be compared
with those reported previously based on morphological and molecular
markers. Congruence between the
DArT phylogeny and previously reported phylogenies (an expected result) will be
interpreted as validation of the DArT array. For S. commersonii, S. bulbocastanum, S. chacoense, and S.
pinnatisectum, parental genotypes have been designated based on crossability studies
and preliminary phenotypic evaluations conducted by our laboratories. F1 mapping populations have been
generated for each species.
Linkage maps will be constructed for each species based on a common set
of DArT markers, allowing comparison of genome structures. Significantly, the maps generated will
allow efficient mapping of genes conditioning agriculturally significant
phenotypes. In support of this
effort, large-scale phenotypic analyses are ongoing. Currently phenotypic tests include evaluation of all
available accessions of S. commersonnii (61 accessions) and S. chacoense
(133
accessions) for foliar resistance to Phytophthora infestans.