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    <title>Nature Precedings - Andrey Ptitsyn</title>
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    <description>Documents posted by Andrey Ptitsyn</description>
    <dc:publisher>Nature Publishing Group</dc:publisher>
    <dc:language>en</dc:language>
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      <title>Transformation of metabolism with age and lifestyle in Antarctic seals: a case study of systems biology approach to cross-species microarray experiment</title>
      <link>http://precedings.nature.com/documents/3380/version/1</link>
      <description>Background: The metabolic transformation that changes Weddell seal pups born on land into aquatic animals is not only interesting for the study of general biology, but it also provides a model for the acquired and congenital muscle disorders which are associated with oxygen metabolism in skeletal muscle. However, the analysis of gene expression in seals is hampered by the lack of specific microarrays and the very limited annotation of known Weddell seal (Leptonychotes weddellii) genes.Results: Muscle samples from newborn, juvenile, and adult Weddell seals were collected during an Antarctic expedition. Extracted RNA was hybridized on Affymetrix Human Expression chips. Preliminary studies showed a detectable signal from at least 7000 probe sets present in all samples and replicates. Relative expression levels for these genes was used for further analysis of the biological pathways implicated in the metabolism transformation which occurs in the transition from newborn, to juvenile, to adult seals. Cytoskeletal remodeling, WNT signaling, FAK signaling, hypoxia-induced HIF1 activation, and insulin regulation were identified as being among the most important biological pathways involved in transformation. Conclusion: In spite of certain losses in specificity and sensitivity, the cross-species application of gene expression microarrays is capable of solving challenging puzzles in biology. A Systems Biology approach based on gene interaction patterns can compensate adequately for the lack of species-specific genomics information.</description>
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      <pubDate>Mon, 29 Jun 2009 09:39:22 UTC</pubDate>
      <dc:title>Transformation of metabolism with age and lifestyle in Antarctic seals: a case study of systems biology approach to cross-species microarray experiment</dc:title>
      <dc:identifier>hdl:10101/npre.2009.3380.1</dc:identifier>
      <dc:date>2009-06-29</dc:date>
      <dc:creator>Andrey Ptitsyn</dc:creator>
      <prism:publicationName>Nature Precedings</prism:publicationName>
      <prism:publicationDate>2009-06-29T09:39:22Z</prism:publicationDate>
      <prism:category>Manuscript</prism:category>
      <prism:section>Developmental Biology</prism:section>
      <prism:section>Ecology</prism:section>
      <prism:section>Bioinformatics</prism:section>
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      <title>Analysis of circadian pattern reveals tissue-specific alternative transcription in leptin signaling pathway</title>
      <link>http://precedings.nature.com/documents/858/version/1</link>
      <description>BackgroundIt has been previously reported that most mammalian genes display a circadian oscillation in their baseline expression. Consequently, the phase and amplitude of each component of a signal transduction cascade has downstream consequences. ResultsWe report our analysis of alternative transcripts in the leptin signaling pathway which is responsible for the systemic regulation of macronutrient storage and energy balance. We focused on the circadian expression pattern of a critical component of the leptin signaling system, suppressor of cytokine signaling 3 (SOCS3). On an Affymetrix GeneChip 430A2 microarray, this gene is represented by three probe sets targeting different regions within the 3&#8217; end of the last exon. We demonstrate that in murine brown adipose tissue two downstream 3&#8217; probe sets experience circadian baseline oscillation in counter-phase to the upstream probe set. Such differences in expression patterns are a telltale sign of alternative splicing within the last exon of SOCS3. In contrast, all three probe sets oscillated in a common phase in murine liver and white adipose tissue.  This suggests that the regulation of SOCS3 expression in brown fat is tissue specific. Another component of the signaling pathway, Janus kinase (JAK), is directly regulated by SOCS and has alternative transcript probe sets oscillating in counter-phase in a white adipose tissue specific manner.ConclusionWe hypothesize that differential oscillation of alternative transcripts may provide a mechanism to maintain steady levels of expression in spite of circadian baseline variation.</description>
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      <pubDate>Thu, 30 Aug 2007 14:51:51 UTC</pubDate>
      <dc:title>Analysis of circadian pattern reveals tissue-specific alternative transcription in leptin signaling pathway</dc:title>
      <dc:identifier>hdl:10101/npre.2007.858.1</dc:identifier>
      <dc:date>2007-08-30</dc:date>
      <dc:creator>Andrey Ptitsyn</dc:creator>
      <prism:publicationName>Nature Precedings</prism:publicationName>
      <prism:publicationDate>2007-08-30T14:51:51Z</prism:publicationDate>
      <prism:category>Manuscript</prism:category>
      <prism:section>Molecular Cell Biology</prism:section>
      <prism:section>Pharmacology</prism:section>
      <prism:section>Bioinformatics</prism:section>
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