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  <title>DRUM Collection: Cell Biology &amp; Molecular Genetics Research Works</title>
  <link rel="alternate" href="http://hdl.handle.net/1903/14" />
  <subtitle />
  <id>http://hdl.handle.net/1903/14</id>
  <updated>2013-05-26T05:38:25Z</updated>
  <dc:date>2013-05-26T05:38:25Z</dc:date>
  <entry>
    <title>Uncovering the evolutionary origin of plant  molecular processes: comparison of Coleochaete  (Coleochaetales) and Spirogyra (Zygnematales)  transcriptomes</title>
    <link rel="alternate" href="http://hdl.handle.net/1903/13371" />
    <author>
      <name>Timme, Ruth E</name>
    </author>
    <author>
      <name>Delwiche, Charles F</name>
    </author>
    <id>http://hdl.handle.net/1903/13371</id>
    <updated>2013-01-11T03:52:37Z</updated>
    <published>2010-05-25T00:00:00Z</published>
    <summary type="text">Title: Uncovering the evolutionary origin of plant  molecular processes: comparison of Coleochaete  (Coleochaetales) and Spirogyra (Zygnematales)  transcriptomes
Authors: Timme, Ruth E; Delwiche, Charles F
Abstract: Background: The large and diverse land plant lineage is nested within a clade of fresh water green algae, the &#xD;
charophytes. Collection of genome-scale data for land plants and other organisms over the past decade has &#xD;
invigorated the field of evolutionary biology. One of the core questions in the field asks: how did a colonization event &#xD;
by a green algae over 450 mya lead to one of the most successful lineages on the tree of life? This question can best be &#xD;
answered using the comparative method, the first step of which is to gather genome-scale data across closely related &#xD;
lineages to land plants. Before sequencing an entire genome it is useful to first gather transcriptome data: it is less &#xD;
expensive, it targets the protein coding regions of the genome, and provides support for gene models for future &#xD;
genome sequencing. We built Expressed Sequence Tag (EST) libraries for two charophyte species, Coleochaete &#xD;
orbicularis (Coleochaetales) and Spirogyra pratensis (Zygnematales). We used both Sanger sequencing and next &#xD;
generation 454 sequencing to cover as much of the transcriptome as possible.&#xD;
Results: Our sequencing effort for Spirogyra pratensis yielded 9,984 5' Sanger reads plus 598,460 GS FLX Standard 454 &#xD;
sequences; Coleochaete orbicularis yielded 4,992 5' Sanger reads plus 673,811 GS FLX Titanium 454 sequences. After &#xD;
clustering S. pratensis yielded 12,000 unique transcripts, or unigenes, and C. orbicularis yielded 19,000. Both &#xD;
transcriptomes were very plant-like, i.e. most of the transcripts were more similar to streptophytes (land plants + &#xD;
charophyte green algae) than to other green algae in the sister group chlorophytes. BLAST results of several land plant &#xD;
genes hypothesized to be important in early land plant evolution resulted in high quality hits in both transcriptomes &#xD;
revealing putative orthologs ripe for follow-up studies.&#xD;
Conclusions: Two main conclusions were drawn from this study. One illustrates the utility of next generation &#xD;
sequencing for transcriptome studies: larger scale data collection at a lower cost enabled us to cover a considerable &#xD;
portion of the transcriptome for both species. And, two, that the charophyte green algal transcriptoms are remarkably &#xD;
plant-like, which gives them the unique capacity to be major players for future evolutionary genomic studies &#xD;
addressing origin of land plant questions.</summary>
    <dc:date>2010-05-25T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Comparative genomic analysis reveals evidence of  two novel Vibrio species closely related to V.  cholerae</title>
    <link rel="alternate" href="http://hdl.handle.net/1903/13370" />
    <author>
      <name>Haley, Bradd J</name>
    </author>
    <author>
      <name>Grim, Christopher J</name>
    </author>
    <author>
      <name>Hasan, Nur A</name>
    </author>
    <author>
      <name>Choi, Seon-Young</name>
    </author>
    <author>
      <name>Chun, Jongsik</name>
    </author>
    <author>
      <name>Brettin, Thomas S</name>
    </author>
    <author>
      <name>Bruce, David C</name>
    </author>
    <author>
      <name>Challacombe, Jean F</name>
    </author>
    <author>
      <name>Detter, J Chris</name>
    </author>
    <author>
      <name>Han, Cliff S</name>
    </author>
    <author>
      <name>Huq, Anwar</name>
    </author>
    <author>
      <name>Colwell, Rita R</name>
    </author>
    <id>http://hdl.handle.net/1903/13370</id>
    <updated>2013-01-11T03:52:06Z</updated>
    <published>2010-05-27T00:00:00Z</published>
    <summary type="text">Title: Comparative genomic analysis reveals evidence of  two novel Vibrio species closely related to V.  cholerae
Authors: Haley, Bradd J; Grim, Christopher J; Hasan, Nur A; Choi, Seon-Young; Chun, Jongsik; Brettin, Thomas S; Bruce, David C; Challacombe, Jean F; Detter, J Chris; Han, Cliff S; Huq, Anwar; Colwell, Rita R
Abstract: Background: In recent years genome sequencing has been used to characterize new bacterial species, a method of &#xD;
analysis available as a result of improved methodology and reduced cost. Included in a constantly expanding list of &#xD;
Vibrio species are several that have been reclassified as novel members of the Vibrionaceae. The description of two &#xD;
putative new Vibrio species, Vibrio sp. RC341 and Vibrio sp. RC586 for which we propose the names V. metecus and V. &#xD;
parilis, respectively, previously characterized as non-toxigenic environmental variants of V. cholerae is presented in this &#xD;
study.&#xD;
Results: Based on results of whole-genome average nucleotide identity (ANI), average amino acid identity (AAI), rpoB &#xD;
similarity, MLSA, and phylogenetic analysis, the new species are concluded to be phylogenetically closely related to V. &#xD;
cholerae and V. mimicus. Vibrio sp. RC341 and Vibrio sp. RC586 demonstrate features characteristic of V. cholerae and V. &#xD;
mimicus, respectively, on differential and selective media, but their genomes show a 12 to 15% divergence (88 to 85% &#xD;
ANI and 92 to 91% AAI) compared to the sequences of V. cholerae and V. mimicus genomes (ANI &lt;95% and AAI &lt;96% &#xD;
indicative of separate species). Vibrio sp. RC341 and Vibrio sp. RC586 share 2104 ORFs (59%) and 2058 ORFs (56%) with &#xD;
the published core genome of V. cholerae and 2956 (82%) and 3048 ORFs (84%) with V. mimicus MB-451, respectively. &#xD;
The novel species share 2926 ORFs with each other (81% Vibrio sp. RC341 and 81% Vibrio sp. RC586). Virulenceassociated factors and genomic islands of V. cholerae and V. mimicus, including VSP-I and II, were found in these &#xD;
environmental Vibrio spp.&#xD;
Conclusions: Results of this analysis demonstrate these two environmental vibrios, previously characterized as variant &#xD;
V. cholerae strains, are new species which have evolved from ancestral lineages of the V. cholerae and V. mimicus clade. &#xD;
The presence of conserved integration loci for genomic islands as well as evidence of horizontal gene transfer between &#xD;
these two new species, V. cholerae, and V. mimicus suggests genomic islands and virulence factors are transferred &#xD;
between these species.</summary>
    <dc:date>2010-05-27T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>The non-pathogenic mycobacteria M. smegmatis and M. fortuitum induce rapid host cell apoptosis via a caspase-3 and TNF dependent pathway</title>
    <link rel="alternate" href="http://hdl.handle.net/1903/13367" />
    <author>
      <name>Bohsali, Amro</name>
    </author>
    <author>
      <name>Abdalla, Hana</name>
    </author>
    <author>
      <name>Velmurugan, Kamalakannan</name>
    </author>
    <author>
      <name>Briken, Volker</name>
    </author>
    <id>http://hdl.handle.net/1903/13367</id>
    <updated>2013-01-11T03:39:23Z</updated>
    <published>2010-09-10T00:00:00Z</published>
    <summary type="text">Title: The non-pathogenic mycobacteria M. smegmatis and M. fortuitum induce rapid host cell apoptosis via a caspase-3 and TNF dependent pathway
Authors: Bohsali, Amro; Abdalla, Hana; Velmurugan, Kamalakannan; Briken, Volker
Abstract: Background: The HIV pandemic raised the potential for facultative-pathogenic mycobacterial species like,&#xD;
Mycobacterium kansasii, to cause disseminating disease in humans with immune deficiencies. In contrast, nonpathogenic mycobacterial species, like M. smegmatis, are not known to cause disseminating disease even in&#xD;
immunocompromised individuals. We hypothesized that this difference in phenotype could be explained by the&#xD;
strong induction of an innate immune response by the non-pathogenic mycobacterial species.&#xD;
Results: A comparison of two rapid-growing, non-pathogenic species (M. smegmatis and M. fortuitum) with two&#xD;
facultative-pathogenic species (M. kansasii and M. bovis BCG) demonstrated that only the non-pathogenic bacteria&#xD;
induced strong apoptosis in human THP-1 cells and murine bone marrow-derived macrophages (BMDM) and&#xD;
dendritic cells (BMDD). The phospho-myo-inositol modification of lipoarabinomannan (PI-LAM) isolated from nonpathogenic species may be one of the cell wall components responsible for the pro-inflammatory activity of the&#xD;
whole bacteria. Indeed, PI-LAM induces high levels of apoptosis and IL-12 expression compared to the mannosyl&#xD;
modification of LAM isolated from facultative-pathogenic mycobacteria. The apoptosis induced by non-pathogenic&#xD;
M. smegmatis was dependent upon caspase-3 activation and TNF secretion. Consistently, BALB/c BMDM responded&#xD;
by secreting large amounts of TNF upon infection with non-pathogenic but not facultative-pathogenic&#xD;
mycobacteria. Interestingly, C57Bl/6 BMDM do not undergo apoptosis upon infection with non-pathogenic&#xD;
mycobacteria despite the fact that they still induce an increase in TNF secretion. This suggests that the host cell&#xD;
signaling pathways are different between these two mouse genotypes and that TNF is necessary but not sufficient&#xD;
to induce host cell apoptosis.&#xD;
Conclusion: These results demonstrate a much stronger induction of the innate immune response by nonpathogenic versus facultative-pathogenic mycobacteria as measured by host cell apoptosis, IL-12 and TNF cytokine&#xD;
induction. These observations lend support to the hypothesis that the strong induction of the innate immune&#xD;
response is a major reason for the lack of pathogenicity in fast-growing mycobacteria.</summary>
    <dc:date>2010-09-10T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Improving pan-genome annotation using whole genome multiple alignment</title>
    <link rel="alternate" href="http://hdl.handle.net/1903/13352" />
    <author>
      <name>Angiuoli, Samuel V</name>
    </author>
    <author>
      <name>Dunning Hotopp, Julie C</name>
    </author>
    <author>
      <name>Salzberg, Steven L</name>
    </author>
    <author>
      <name>Tettelin, Herve</name>
    </author>
    <id>http://hdl.handle.net/1903/13352</id>
    <updated>2013-01-11T03:46:30Z</updated>
    <published>2011-06-30T00:00:00Z</published>
    <summary type="text">Title: Improving pan-genome annotation using whole genome multiple alignment
Authors: Angiuoli, Samuel V; Dunning Hotopp, Julie C; Salzberg, Steven L; Tettelin, Herve
Abstract: Background: Rapid annotation and comparisons of genomes from multiple isolates (pan-genomes) is becoming&#xD;
commonplace due to advances in sequencing technology. Genome annotations can contain inconsistencies and&#xD;
errors that hinder comparative analysis even within a single species. Tools are needed to compare and improve&#xD;
annotation quality across sets of closely related genomes.&#xD;
Results: We introduce a new tool, Mugsy-Annotator, that identifies orthologs and evaluates annotation quality in&#xD;
prokaryotic genomes using whole genome multiple alignment. Mugsy-Annotator identifies anomalies in annotated&#xD;
gene structures, including inconsistently located translation initiation sites and disrupted genes due to draft&#xD;
genome sequencing or pseudogenes. An evaluation of species pan-genomes using the tool indicates that such&#xD;
anomalies are common, especially at translation initiation sites. Mugsy-Annotator reports alternate annotations that&#xD;
improve consistency and are candidates for further review.&#xD;
Conclusions: Whole genome multiple alignment can be used to efficiently identify orthologs and annotation&#xD;
problem areas in a bacterial pan-genome. Comparisons of annotated gene structures within a species may show&#xD;
more variation than is actually present in the genome, indicating errors in genome annotation. Our new tool&#xD;
Mugsy-Annotator assists re-annotation efforts by highlighting edits that improve annotation consistency.</summary>
    <dc:date>2011-06-30T00:00:00Z</dc:date>
  </entry>
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