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<title>Edward Himelblau</title>
<copyright>Copyright (c) 2012  All rights reserved.</copyright>
<link>http://works.bepress.com/ehimelbl</link>
<description>Recent documents in Edward Himelblau</description>
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<title>FLOWERING LOCUS C Influences the Timing of Shoot Maturation in &lt;em&gt;Arabidopsis thaliana&lt;/em&gt;</title>
<link>http://works.bepress.com/ehimelbl/8</link>
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<pubDate>Wed, 09 Feb 2011 09:11:16 PST</pubDate>
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<author>Laurie Mentzer et al.</author>


<category>Articles</category>

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<title>Global Warming</title>
<link>http://works.bepress.com/ehimelbl/7</link>
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<pubDate>Tue, 27 Apr 2010 15:24:34 PDT</pubDate>
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<author>Edward Himelblau</author>


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<title>Integration of Flowering Signals in Winter-Annual Arabidopsis</title>
<link>http://works.bepress.com/ehimelbl/6</link>
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<pubDate>Tue, 27 Apr 2010 15:24:34 PDT</pubDate>
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	<p>Photoperiod is the primary environmental factor affecting flowering time in rapid-cycling accessions of Arabidopsis (<em>Arabidopsis thaliana</em>). Winter-annual Arabidopsis, in contrast, have both a photoperiod and a vernalization requirement for rapid flowering. In winter annuals, high levels of the floral inhibitor <em>FLC</em> (<em>FLOWERING LOCUS C</em>) suppress flowering prior to vernalization. <em>FLC</em> acts to delay flowering, in part, by suppressing expression of the floral promoter <em>SOC1</em> (<em>SUPPRESSOR OF OVEREXPRESSION OF CONSTANS1</em>). Vernalization leads to a permanent epigenetic suppression of <em>FLC</em>. To investigate how winter-annual accessions integrate signals from the photoperiod and vernalization pathways, we have examined activation-tagged alleles of <em>FT</em> and the  <em>FT</em> homolog,  <em>TSF</em> ( <em>TWIN SISTER OF FT</em>), in a winter-annual background. Activation of  <em>FT</em> or  <em>TSF</em> strongly suppresses the  <em>FLC</em>-mediated late-flowering phenotype of winter annuals; however,  <em>FT</em> and  <em>TSF</em> overexpression does not affect  <em>FLC</em> mRNA levels. Rather,  <em>FT</em> and  <em>TSF</em> bypass the block to flowering created by  <em>FLC</em> by activating  <em>SOC1</em> expression. We have also found that  <em>FLC</em> acts as a dosage-dependent inhibitor of  <em>FT</em> expression. Thus, the integration of flowering signals from the photoperiod and vernalization pathways occurs, at least in part, through the regulation of  <em>FT</em>,  <em>TSF</em>, and  <em>SOC1</em>.</p>

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<author>Scott D. Michaels et al.</author>


<category>Articles</category>

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<title>Molecular Aspect of Leaf Senescence</title>
<link>http://works.bepress.com/ehimelbl/5</link>
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<pubDate>Tue, 27 Apr 2010 15:24:33 PDT</pubDate>
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	<p>Senescence is the last stage of leaf development and one type of programmed cell death that occurs in plants. The relationships among senescence programs that are induced by a variety of factors have been addressed at a molecular level in recent studies. Furthermore, an overlap between the pathogen-response and senescence programs is beginning to be characterized. The complexity of the senescence program is also evident in studies of senescence-specific gene regulation and the role of photosynthesis and plant hormones in senescence regulation. New molecular-genetic approaches are expected to be useful in unraveling the molecular mechanisms of the leaf senescence program.</p>

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<author>Edward Himelblau et al.</author>


<category>Articles</category>

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<title>Delivering Copper Within Plant Cells</title>
<link>http://works.bepress.com/ehimelbl/4</link>
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<pubDate>Tue, 27 Apr 2010 15:24:33 PDT</pubDate>
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	<p>Two genes recently identified in Arabidopsis thaliana may be involved in sequestering free copper ions in the cytoplasm and delivering copper to post-Golgi vesicles. The genes <em>COPPER CHAPERONE</em> and <em>RESPONSIVE TO ANTAGONIST1</em> are homologous to copper-trafficking genes from yeast and humans. This plant copper-delivery pathway is required to create functional ethylene receptors. The pathway may also facilitate the transport of copper from senescing leaf tissue. In addition, several other genes have been identified recently that may have a role in copper salvage during senescence.</p>

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<author>Edward Himelblau et al.</author>


<category>Articles</category>

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<title>Forward and Reverse Genetics of Rapid-Cycling &lt;em&gt;Brassica oleracea&lt;/em&gt;</title>
<link>http://works.bepress.com/ehimelbl/3</link>
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<pubDate>Tue, 27 Apr 2010 15:24:32 PDT</pubDate>
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	<p>Seeds of rapid-cycling <em>Brassica oleracea</em> were mutagenized with the chemical mutagen, ethylmethane sulfonate. The reverse genetics technique, TILLING, was used on a sample population of 1,000 plants, to determine the mutation profile. The spectrum and frequency of mutations induced by ethylmethane sulfonate was similar to that seen in other diploid species such as <em>Arabidopsis thaliana</em>. These data indicate that the mutagenesis was effective and demonstrate that TILLING represents an efficient reverse genetic technique in <em>B. oleracea</em> that will become more valuable as increasing genomic sequence data become available for this species. The extensive duplication in the <em>B. oleracea</em> genome is believed to result in the genetic redundancy that has been important for the evolution of morphological diversity seen in today's <em>B. oleracea</em> crops (broccoli, Brussels sprouts, cauliflower, cabbage, kale and kohlrabi). However, our forward genetic screens identified 120 mutants in which some aspect of development was affected. Some of these lines have been characterized genetically and in the majority of these, the mutant trait segregates as a recessive allele affecting a single locus. One dominant mutation (<em>curly leaves</em>) and one semi-dominant mutation (<em>dwarf-like</em>) were also identified. Allelism tests of two groups of mutants (<em>glossy</em> and <em>dwarf</em>) revealed that for some loci, multiple independent alleles have been identified. These data indicate that, despite genetic redundancy, mutation of many individual loci in <em>B. oleracea</em> results in distinct phenotypes.</p>

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<author>Edward Himelblau et al.</author>


<category>Articles</category>

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<title>Identification of a Functional Homolog of the Yeast Copper Homeostasis Gene ATX1 From Arabidopsis</title>
<link>http://works.bepress.com/ehimelbl/2</link>
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<pubDate>Tue, 27 Apr 2010 15:24:32 PDT</pubDate>
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	<p>A cDNA clone encoding a homolog of the yeast (<em>Saccharomyces cerevisiae</em>) gene Anti-oxidant 1 (<em>ATX1</em>) has been identified from Arabidopsis. This gene, referred to as <em>Copper CHaperone</em> (<em>CCH</em>), encodes a protein that is 36% identical to the amino acid sequence of <em>ATX1</em> and has a 48-amino acid extension at the C-terminal end, which is absent from <em>ATX1</em> homologs identified in animals. <em>ATX1</em>-deficient yeast (<em>atx1</em>) displayed a loss of high-affinity iron uptake. Expression of <em>CCH</em> in the <em>atx1</em> strain restored high-affinity iron uptake, demonstrating that <em>CCH</em> is a functional homolog of <em>ATX1</em>. When overexpressed in yeast lacking the superoxide dismutase gene <em>SOD1</em>, both <em>ATX1</em> and <em>CCH</em> protected the cell from the reactive oxygen toxicity that results from superoxide dismutase deficiency. <em>CCH</em> was unable to rescue the sod1 phenotype in the absence of copper, indicating that <em>CCH</em> function is copper dependent. In Arabidopsis <em>CCH</em> mRNA is present in the root, leaf, and inflorescence and is up-regulated 7-fold in leaves undergoing senescence. In plants treated with 800 nL/L ozone for 30 min, <em>CCH</em> mRNA levels increased by 30%. In excised leaves and whole plants treated with high levels of exogenous CuSO4, <em>CCH</em> mRNA levels decreased, indicating that <em>CCH</em> is regulated differently than characterized metallothionein proteins in Arabidopsis.</p>

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<author>Edward Himelblau et al.</author>


<category>Articles</category>

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<item>
<title>The Expression Pattern of the Tonoplast Intrinsic Protein γ-TIP in &lt;em&gt;Arabidopsis thaliana&lt;/em&gt; Is Correlated With Cell Enlargement</title>
<link>http://works.bepress.com/ehimelbl/1</link>
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<pubDate>Tue, 27 Apr 2010 15:24:32 PDT</pubDate>
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	<p>The vacuolar membrane (tonoplast) contains an abundant intrinsic protein with six membrane-spanning domains that is encoded by a small gene family. Different isoforms of tonoplast intrinsic protein (TIP) are expressed in different tissues or as a result of specific signals. Using promoter-β-glucuronidase (GUS) fusions and in situ hybridization, we have examined the expression of γ-TIP in <em>Arabidopsis thaliana</em>. GUS staining of plants transformed with promoter-GUS fusions showed that γ-TIP gene expression is high in recently formed tissues of young roots. In the shoot, γ-TIP gene expression was highest in the vascular bundles of stems and petioles, as well as in the stipules and in the receptacle of the flower. No GUS activity was detected in root or shoot meristems or in older tissues, suggesting temporal control of γ-TIP gene expression associated with cell elongation and/or differentiation. In situ hybridization carried out with whole seedlings confirmed that in root tips, γ-TIP mRNA was present only in the zone of cell elongation just behind the apical meristem. In seedling shoots, mRNA abundance was also found to be correlated with cell expansion. These results indicate that γ-TIP may be expressed primarily at the time when the large central vacuoles are being formed during cell enlargement.</p>

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<author>Edward Himelblau et al.</author>


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