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    <mx:record id="9161">
        <mx:leader/>
        <datafield tag="022" ind1="" ind2="">
            <subfield code="a">1554-8627</subfield>
        </datafield>
        <datafield tag="100" ind1="" ind2="">
            <subfield code="a">Bo Dong</subfield>
            <subfield code="a">Xiao-Hong Liu</subfield>
            <subfield code="a">Jian-Ping Lu</subfield>
            <subfield code="a">Fu-Sheng Zhang</subfield>
            <subfield code="a">Hui-Min Gao</subfield>
            <subfield code="a">Hong-Kai Wang and Fu-Cheng Lin</subfield>
        </datafield>
        
        <datafield tag="210" ind1="" ind2="">
            <subfield code="a">autophagy</subfield>
        </datafield>
        
        <datafield tag="245" ind1="" ind2="">
            <subfield code="a">MgAtg9 trafficking in &lt;em&gt;Magnaporthe oryzae&lt;/em&gt;</subfield> 
        </datafield>
        
        <datafield tag="260" ind1="3" ind2="">
            <subfield code="b">Landes Bioscience</subfield>
            <subfield code="c">2009-10-01</subfield>
        </datafield>
        
        <datafield tag="302" ind1="" ind2="">
            <subfield code="a">946 - 953</subfield>
        </datafield>
        
        <datafield tag="440" ind1="" ind2="">
            
            <subfield code="a">Autophagy</subfield>
            <subfield code="v">5-7</subfield>
        </datafield>
        <datafield tag="449" ind1="" ind2="">
            <subfield code="o">Landes Bioscience</subfield>
        </datafield>
        <datafield tag="520" ind1="3" ind2="">
            <subfield code="a">Autophagy is a vacuolar/lysosomal cytoplasmic recycling system in eukaryotic cells. &lt;em&gt;ScATG9&lt;/em&gt; is indispensable for autophagy in &lt;em&gt;Saccharomyces cerevisiae&lt;/em&gt;. Here, we deleted &lt;em&gt;MgATG9&lt;/em&gt;, the orthologue of &lt;em&gt;ScATG9&lt;/em&gt;, via targeted gene replacement in the phytopathogenic filamentous fungus &lt;em&gt;Magnaporthe oryzae&lt;/em&gt;, and then analyzed the cellular distribution pattern of EGFP-MgAtg9 in the &lt;em&gt;Mgatg9∆&lt;/em&gt; mutant. We detected an expression profile of multiple green dots in the conidial cell inoculated in rich media and in the appressoria differentiated from the conidia in H&lt;sub&gt;2&lt;/sub&gt;O. Concurrent with the punctation, we found some fluorescent signals localized on the central vacuole of the submerged hyphae from the conidia cultured in rich media. Next, we introduced DsRed2-MgAtg8 into the &lt;em&gt;Mgatg9∆ &lt;/em&gt;mutant expressing EGFP-MgAtg9 and observed partial overlap at multiple sites in the conidial cell, reminiscent of that in the mammalian system. Our findings further led to the postulation that the multiple sites where the two fusions colocalized tend to merge as a central structure in the conidial cell. Finally, we tested the expression of EGFP-MgAtg9 in null mutants of &lt;em&gt;MgATG1&lt;/em&gt;, &lt;em&gt;2&lt;/em&gt;, &lt;em&gt;13&lt;/em&gt; and &lt;em&gt;18&lt;/em&gt;, respectively. We speculate that MgAtg1, 2 and 18, but not MgAtg13, is required for MgAtg9 cycling through the multiple colocalization sites to its storage pools in the conidial cell of&lt;em&gt; M. oryzae&lt;/em&gt;, and fusion of these colocalization sites into a central structure could be governed through other unidentified mechanisms.</subfield>
        </datafield>
        <datafield tag="856" ind1="4" ind2="">
            
            <subfield code="u">http://dx.doi.org/10.4161/auto.5.7.9161</subfield>
            <subfield code="u">http://www.landesbioscience.com/journals/autophagy/article/9161/</subfield>
        </datafield>
 
        <datafield tag="949" ind1="" ind2="">
            <subfield code="t">article</subfield>
            <subfield code="n">Basic Research Paper</subfield>
        </datafield>
    </mx:record>

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