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<title>PLANT PHYSIOLOGY GENOME ANALYSIS</title>
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<description>PLANT PHYSIOLOGY RSS feed -- recent GENOME ANALYSIS articles</description>
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<title>PLANT PHYSIOLOGY</title>
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<title><![CDATA[[GENOME ANALYSIS] A Genome-Wide Functional Investigation into the Roles of Receptor-Like Proteins in Arabidopsis]]></title>
<link>http://www.plantphysiol.org/cgi/content/short/147/2/503?rss=1</link>
<description><![CDATA[
<p>Receptor-like proteins (RLPs) are cell surface receptors that typically consist of an extracellular leucine-rich repeat domain, a transmembrane domain, and a short cytoplasmatic tail. In several plant species, RLPs have been found to play a role in disease resistance, such as the tomato (<I>Solanum lycopersicum</I>) Cf and Ve proteins and the apple (<I>Malus domestica</I>) HcrVf2 protein that mediate resistance against the fungal pathogens <I>Cladosporium fulvum</I>, <I>Verticillium</I> spp., and <I>Venturia inaequalis</I>, respectively. In addition, RLPs play a role in plant development; Arabidopsis (<I>Arabidopsis thaliana</I>) TOO MANY MOUTHS (TMM) regulates stomatal distribution, while Arabidopsis CLAVATA2 (CLV2) and its functional maize (<I>Zea mays</I>) ortholog FASCINATED EAR2 regulate meristem maintenance. In total, 57 <I>RLP</I> genes have been identified in the Arabidopsis genome and a genome-wide collection of T-DNA insertion lines was assembled. This collection was functionally analyzed with respect to plant growth and development and sensitivity to various stress responses, including susceptibility toward pathogens. A number of novel developmental phenotypes were revealed for our <I>CLV2</I> and <I>TMM</I> insertion mutants. In addition, one <I>AtRLP</I> gene was found to mediate abscisic acid sensitivity and another <I>AtRLP</I> gene was found to influence nonhost resistance toward <I>Pseudomonas syringae</I> pv <I>phaseolicola</I>. This genome-wide collection of Arabidopsis <I>RLP</I> gene T-DNA insertion mutants provides a tool for future investigations into the biological roles of RLPs.</p>
]]></description>
<dc:creator><![CDATA[Wang, G., Ellendorff, U., Kemp, B., Mansfield, J. W., Forsyth, A., Mitchell, K., Bastas, K., Liu, C.-M., Woods-Tor, A., Zipfel, C., de Wit, P. J.G.M., Jones, J. D.G., Tor, M., Thomma, B. P.H.J.]]></dc:creator>
<dc:date>2008-06-04</dc:date>
<dc:identifier>info:doi/10.1104/pp.108.119487</dc:identifier>
<dc:title><![CDATA[[GENOME ANALYSIS] A Genome-Wide Functional Investigation into the Roles of Receptor-Like Proteins in Arabidopsis]]></dc:title>
<dc:publisher>American Society of Plant Biologists</dc:publisher>
<prism:number>2</prism:number>
<prism:volume>147</prism:volume>
<prism:endingPage>517</prism:endingPage>
<prism:publicationDate>2008-06-01</prism:publicationDate>
<prism:startingPage>503</prism:startingPage>
<prism:section>GENOME ANALYSIS</prism:section>
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<title><![CDATA[[GENOME ANALYSIS] Deregulation of Maize C4 Photosynthetic Development in a Mesophyll Cell-Defective Mutant]]></title>
<link>http://www.plantphysiol.org/cgi/content/short/146/4/1469?rss=1</link>
<description><![CDATA[
<p>During maize (<I>Zea mays</I>) C<SUB>4</SUB> differentiation, mesophyll (M) and bundle sheath (BS) cells accumulate distinct sets of photosynthetic enzymes, with very low photosystem II (PSII) content in BS chloroplasts. Consequently, there is little linear electron transport in the BS and ATP is generated by cyclic electron flow. In contrast, M thylakoids are very similar to those of C<SUB>3</SUB> plants and produce the ATP and NADPH that drive metabolic activities. Regulation of this differentiation process is poorly understood, but involves expression and coordination of nuclear and plastid genomes. Here, we identify a recessive allele of the maize high chlorophyll fluorescence (<I>Hcf136</I>) homolog that in Arabidopsis (<I>Arabidopsis thaliana</I>) functions as a PSII stability or assembly factor located in the thylakoid lumen. Proteome analysis of the thylakoids and electron microscopy reveal that <I>Zmhcf136</I> lacks PSII complexes and grana thylakoids in M chloroplasts, consistent with the previously defined Arabidopsis function. Interestingly, <I>hcf136</I> is also defective in processing the full-length <I>psbB-psbT-psbH-petB-petD</I> polycistron specifically in M chloroplasts. To determine whether the loss of PSII in M cells affects C<SUB>4</SUB> differentiation, we performed cell-type-specific transcript analysis of <I>hcf136</I> and wild-type seedlings. The results indicate that M and BS cells respond uniquely to the loss of PSII, with little overlap in gene expression changes between data sets. These results are discussed in the context of signals that may drive differential gene expression in C<SUB>4</SUB> photosynthesis.</p>
]]></description>
<dc:creator><![CDATA[Covshoff, S., Majeran, W., Liu, P., Kolkman, J. M., van Wijk, K. J., Brutnell, T. P.]]></dc:creator>
<dc:date>2008-04-03</dc:date>
<dc:identifier>info:doi/10.1104/pp.107.113423</dc:identifier>
<dc:title><![CDATA[[GENOME ANALYSIS] Deregulation of Maize C4 Photosynthetic Development in a Mesophyll Cell-Defective Mutant]]></dc:title>
<dc:publisher>American Society of Plant Biologists</dc:publisher>
<prism:number>4</prism:number>
<prism:volume>146</prism:volume>
<prism:endingPage>1481</prism:endingPage>
<prism:publicationDate>2008-04-01</prism:publicationDate>
<prism:startingPage>1469</prism:startingPage>
<prism:section>GENOME ANALYSIS</prism:section>
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