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      Characterization of a Human 12/15-Lipoxygenase Promoter Variant Associated with Atherosclerosis Identifies Vimentin as a Promoter Binding Protein

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          Abstract

          Background

          Sequence variation in the human 12/15 lipoxygenase (ALOX15) has been associated with atherosclerotic disease. We functionally characterized an ALOX15 promoter polymorphism, rs2255888, previously associated with carotid plaque burden.

          Methodology/Principal Findings

          We demonstrate specific in vitro and in vivo binding of the cytoskeletal protein, vimentin, to the ALOX15 promoter. We show that the two promoter haplotypes carrying alternate alleles at rs2255888 exhibit significant differences in promoter activity by luciferase reporter assay in two cell lines. Differences in i n-vitro vimentin-binding to and formation of DNA secondary structures in the polymorphic promoter sequence are also detected by electrophoretic mobility shift assay and biophysical analysis, respectively. We show regulation of ALOX15 protein by vimentin.

          Conclusions/Significance

          This study suggests that vimentin binds the ALOX15 promoter and regulates its promoter activity and protein expression. Sequence variation that results in changes in DNA conformation and vimentin binding to the promoter may be relevant to ALOX15 gene regulation.

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          Most cited references38

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          Following G-quartet formation by UV-spectroscopy.

          Oligodeoxynucleotides which include stretches of guanines form a well-known tetrameric structure. We show that the recording of reversible absorbance changes at 295 nm allows to precisely monitor intramolecular guanine (G)-quartet formation and dissociation. Accurate Tm and thermodynamic values could be easily extracted from the data, whereas classical recordings at 260 nm led to a much larger uncertainty and in extreme cases, to completely inaccurate measurements. This inverted denaturation profile was observed for all G-quartet-forming oligonucleotides studied so far. This technique is very useful in all cases where intramolecular or intermolecular quadruplex formation is suspected.
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            Vimentin is secreted by activated macrophages.

            Vimentin is a widely expressed intermediate filament protein thought to be involved mainly in structural processes, such as wound healing. We now demonstrate that activated human macrophages secrete vimentin into the extracellular space. The maturation of blood-derived monocytes into macrophages involves several signalling pathways. We show that secretion of vimentin, which is phosphorylated at serine and threonine residues, is enhanced by the phosphatase inhibitor okadaic acid and blocked by the specific protein kinase C inhibitor GO6983. These findings are consistent with previous observations that phosphorylation of vimentin affects its intracellular localization and that vimentin is a substrate for protein kinase C (PKC). We also show that the anti-inflammatory cytokine interleukin-10 (IL-10), which inhibits PKC activity, blocks secretion of vimentin. In contrast, the pro-inflammatory cytokine tumour necrosis factor alpha (TNF-alpha) can trigger secretion of vimentin. Finally, we found that extracellular vimentin is involved in bacterial killing and the generation of oxidative metabolites, two important functions of activated macrophages. These data establish that vimentin is secreted by macrophages in response to pro-inflammatory signalling pathways and is probably involved in immune function.
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              Thermal difference spectra: a specific signature for nucleic acid structures

              We show that nucleic acid structures may be conveniently and inexpensively characterized by their UV thermal difference spectra. A thermal difference spectrum (TDS) is obtained for a nucleic acid by simply recording the ultraviolet absorbance spectra of the unfolded and folded states at temperatures above and below its melting temperature (T m). The difference between these two spectra is the TDS. The TDS has a specific shape that is unique for each type of nucleic acid structure, a conclusion that is based on a comparison of >900 spectra from 200 different sequences. The shape of the TDS reflects the subtleties of base stacking interactions that occur uniquely within each type of nucleic acid structure. TDS provides a simple, inexpensive and rapid method to obtain structural insight into nucleic acid structures, which is applicable to both DNA and RNA from short oligomers to polynucleotides. TDS complements circular dichroism as a tool for the structural characterization of nucleic acids in solution.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2012
                7 August 2012
                : 7
                : 8
                : e42417
                Affiliations
                [1 ]Research Center for Human Genetics, Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, Texas, United States of America
                [2 ]Centers for Proteomics and Systems Biology, Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, Texas, United States of America
                [3 ]Human Genetics Center, School of Public Health, University of Texas Health Science Center at Houston, Houston, Texas, United States of America
                [4 ]Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, Texas, United States of America
                [5 ]Department of Biochemistry & Cell Biology, Rice University, Houston, Texas, United States of America
                [6 ]Department of Molecular Pathology, M.D. Anderson Cancer Center, Houston, Texas, United States of America
                University Medical Center Utrecht, The Netherlands
                Author notes

                Competing Interests: The author has declared that no competing interests exist.

                [¤a]

                Current address: Baylor College of Medicine, Houston, Texas, United States of America

                [¤b]

                Current address: Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America

                Contributed reagents/material: MF. Contributed instrument: DG. Planned the work: SS MF. Designed and executed the experiments: SS. Performed Thermal Melt experiment: SS KA. Ran NMR instrument: SM. Ran Mass Spec instrument: DH. Analyzed Thermal Melt experiment: KA. Analyzed NMR data: SM. Analyzed Mass Spec data: DH. Wrote the whole manuscript: SS. Edited and rewrote some portions of the manuscript: MF. Wrote material/method and text for thermal melt: KA. Wrote material/method for NMR: SM. Wrote material/method for mass spec: DH. Edited the manuscript: DG KA SM DH.

                Article
                PONE-D-12-10161
                10.1371/journal.pone.0042417
                3413658
                22879973
                79632a6a-b7b8-484e-b196-ee0c791228b8
                Copyright @ 2012

                This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.

                History
                : 10 April 2012
                : 4 July 2012
                Page count
                Pages: 10
                Funding
                This research was supported by grant HL084099 from the National Heart Lung and Blood Institute to MF. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology
                Biochemistry
                Enzymes
                Enzyme Regulation
                Nucleic Acids
                DNA
                Proteins
                Cytoskeletal Proteins
                DNA-binding proteins
                Molecular Cell Biology
                Nucleic Acids
                DNA
                Gene Expression
                Medicine
                Cardiovascular
                Atherosclerosis

                Uncategorized
                Uncategorized

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