EFS12- Book of abstracts - Contact
EFS12- Book of abstracts - Contact
EFS12- Book of abstracts - Contact
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SESSION 4: GENETICS OF HOSTS – PLANT RESISTANCE TO FUSARIUM,<br />
VARIETY DEVELOPMENT<br />
P101 - Functional characterization <strong>of</strong> a lipid transfer<br />
protein associated with Qfhs.ifa-5A<br />
G. Siegwart, J. J. Peter, W. Schweiger, H. Buerstmayr<br />
BOKU - University <strong>of</strong> Natural Resources and Life Sciences, A-1180 Vienna - Department for<br />
Biotechnology in Plant production, A-3430 Tulln<br />
E-mail: gerald.siegwart@boku.ac.at<br />
Fusarium head blight (FHB) is a substantial disease for wheat and other small<br />
grain cereals. Resistance is generated by many QTL, all providing a distinct part<br />
to the mutually produced quantitative resistance. Beneath these many QTL, two<br />
<strong>of</strong> them are outstanding as they provide together about 40% <strong>of</strong> the total<br />
resistance – these QTL are designated Fhb1 and Qfhs.ifa-5A. (Buerstmayr 2002,<br />
Buerstmayr 2003). It is not known which or how many genes are responsible for<br />
the effect <strong>of</strong> these QTL, but potential candidates could be used as target for virusinduced<br />
gene silencing (VIGS) in order to transiently silence the gene and hence<br />
experience differences in spread <strong>of</strong> the disease. A candidate gene that was<br />
shown strongly associated with the major type I resistance QTL Qfhs.ifa-5A in<br />
Affymetrix microarray as well as in RNA-seq encodes a Lipid transfer protein<br />
(LTP). LTPs are small and abundant proteins involved in membrane biosynthesis,<br />
lipid trafficking, cutin/suberin formation as well as in stress response and defense<br />
against bacterial or fungal pathogens. (Kirubakaran, 2008)The candidate<br />
emerged due to its high upregulation (150x), when comparing mock-inoculated<br />
near-isogenic lines (NIL) that only differed in Qfhs.ifa-5A, suggesting constitutive<br />
expression associated with the QTL. We mapped the LTP close to the centromere<br />
on chromosome 5AL, proving that it only seems to be associated with Qfhs.ifa-5A,<br />
but not the causal protein itself, as this is located on 5AS. Nevertheless there is a<br />
strong connection between the LTP and the QTL, so we subjected it to our VIGSpipeline.<br />
We transiently silenced the gene in a NIL only harboring Qfhs.ifa-5A,<br />
which should facilitate comparison between silenced- and control plants. We<br />
observed a faster spread <strong>of</strong> disease symptoms and earlier wilting, compared to<br />
controls. Results <strong>of</strong> two independent biological replications using two different<br />
silencing-constructs both times as well as qPCR validation will be presented.<br />
Keywords: LTP, Virus induced gene silencing, Qfhs.ifa-5A, wheat<br />
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