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590<br />

Gopi K. Podila and Luisa Lanfranco<br />

Table 2. Differential expression of selected interaction clones from L. bicolor. Clones are<br />

selected from macroarray analysis. The E ratio was calculated by comparing the expression<br />

levels in the interacted fungal tissue with those in the free-living fungus using<br />

macroarrays<br />

GenBank no. E value Database match Expression<br />

ratio<br />

BI094576 3e –69 BiP protein (Aspergillus nidulans) 4.10<br />

BI094582 2e –69 PF6.2.1 (Laccaria bicolor) 8.00<br />

BI094583 2e –48 a-tubulin (Ustilago maydis) 4.51<br />

BI094587 1e –10 Homeobox genes Hox-2.6 (Mus musculus) 3.30<br />

BI094592 2e –10 PEP carboxykinase (Mus musculus) 4.33<br />

BI094601 2e –63 LbAut7 (L. bicolor) 3.73<br />

BI094606 3e –09 b-importin (Schizosaccharomyces pombe) 4.43<br />

BI094612 2e –35 Malate synthase (L. bicolor) 3.82<br />

BI094615 9e –36 TEF (EF1a) (Schizophyllum commune) 3.61<br />

BI094619 1e –06 IRS 1-like protein (Xenopus laevis) 3.13<br />

BI094621 1e –31 Ras related protein (L. bicolor) 3.81<br />

BI094622 3e –86 AAD (Phanerochate. chrysosporium) 2.61<br />

BI094623 1e –06 LZK protein kinase (Homo sapiens) 2.90<br />

BI094629 7e –13 Lactonohydrolase (Fusarium oxysporum) 3.91<br />

BI094632 9e –27 E-MAP-115 (H. sapiens) 4.21<br />

BI094635 1e –26 SUG1 subunit 8 (S. cerevisiae) 4.61<br />

BI094639 1e –16 Septin Spn3 (S. pombe) 3.92<br />

BI094653 5e –62 Rho GTPase (S. cerevisiae) 3.21<br />

BI094657 1e –10 Clathrin adapter protein (A. thaliana) 2.08<br />

BI094660 6e –21 AcetylCoA acetyltransferase (L. bicolor) 4.25<br />

BI094667 1e –20 b-transducin (S. pombe) 4.11<br />

BI094676 2e –37 Chitin synthase I (U. maydis) 3.71<br />

shown in Fig. 6.An E ratio that indicates the relative increase in the expression<br />

of each gene in the interaction over the free-living state is used to quantitate<br />

differential expression. There is an overall increase in levels of expression of<br />

several clones tested (Fig. 7). The scatter plot of the normalized data from signal<br />

analysis of the membranes is presented in Fig. 8, which shows global<br />

changes in the expression of interaction related genes. Levels of expression of<br />

selected genes from 72-h interaction are listed in Table 2.<br />

12 Conclusions<br />

The EST and macroarray approaches provide efficient tools for mycorrhizal<br />

symbiosis research. These approaches have the resolution and ability to<br />

obtain a more comprehensive view of various stages of mycorrhiza development<br />

or treatment effects due to nutritional changes or differences due to host

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