62
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      The late‐annotated small ORF LSO1 is a target gene of the iron regulon of Saccharomyces cerevisiae

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          We have identified a new downstream target gene of the Aft1/2‐regulated iron regulon in budding yeast Saccharomyces cerevisiae, the late‐annotated small open reading frame LSO1 . LSO1 transcript is among the most highly induced from a transcriptome analysis of a fet3‐1 mutant grown in the presence of the iron chelator bathophenanthrolinedisulfonic acid. LSO1 has a paralog, LSO2 , which is constitutively expressed and not affected by iron availability. In contrast, we find that the LSO1 promoter region contains three consensus binding sites for the Aft1/2 transcription factors and that an LSO1‐lacZ reporter is highly induced under low‐iron conditions in a Aft1‐dependent manner. The expression patterns of the Lso1 and Lso2 proteins mirror those of their mRNAs. Both proteins are localized to the nucleus and cytoplasm, but become more cytoplasmic upon iron deprivation consistent with a role in iron transport. LSO1 and LSO2 appear to play overlapping roles in the cellular response to iron starvation since single lso1 and lso2 mutants are sensitive to iron deprivation and this sensitivity is exacerbated when both genes are deleted.

          Related collections

          Most cited references37

          • Record: found
          • Abstract: found
          • Article: not found

          Finding functional features in Saccharomyces genomes by phylogenetic footprinting.

          The sifting and winnowing of DNA sequence that occur during evolution cause nonfunctional sequences to diverge, leaving phylogenetic footprints of functional sequence elements in comparisons of genome sequences. We searched for such footprints among the genome sequences of six Saccharomyces species and identified potentially functional sequences. Comparison of these sequences allowed us to revise the catalog of yeast genes and identify sequence motifs that may be targets of transcriptional regulatory proteins. Some of these conserved sequence motifs reside upstream of genes with similar functional annotations or similar expression patterns or those bound by the same transcription factor and are thus good candidates for functional regulatory sequences.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Life with 6000 genes.

            The genome of the yeast Saccharomyces cerevisiae has been completely sequenced through a worldwide collaboration. The sequence of 12,068 kilobases defines 5885 potential protein-encoding genes, approximately 140 genes specifying ribosomal RNA, 40 genes for small nuclear RNA molecules, and 275 transfer RNA genes. In addition, the complete sequence provides information about the higher order organization of yeast's 16 chromosomes and allows some insight into their evolutionary history. The genome shows a considerable amount of apparent genetic redundancy, and one of the major problems to be tackled during the next stage of the yeast genome project is to elucidate the biological functions of all of these genes.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Metal Preferences and Metallation*

              The metal binding preferences of most metalloproteins do not match their metal requirements. Thus, metallation of an estimated 30% of metalloenzymes is aided by metal delivery systems, with ∼25% acquiring preassembled metal cofactors. The remaining ∼70% are presumed to compete for metals from buffered metal pools. Metallation is further aided by maintaining the relative concentrations of these pools as an inverse function of the stabilities of the respective metal complexes. For example, magnesium enzymes always prefer to bind zinc, and these metals dominate the metalloenzymes without metal delivery systems. Therefore, the buffered concentration of zinc is held at least a million-fold below magnesium inside most cells.
                Bookmark

                Author and article information

                Journal
                Microbiologyopen
                Microbiologyopen
                10.1002/(ISSN)2045-8827
                MBO3
                MicrobiologyOpen
                John Wiley and Sons Inc. (Hoboken )
                2045-8827
                08 October 2015
                December 2015
                : 4
                : 6 ( doiID: 10.1002/mbo3.2015.4.issue-6 )
                : 941-951
                Affiliations
                [ 1 ] Department of Biochemistry and Molecular GeneticsUniversity of Colorado School of Medicine Aurora Colorado 80045
                [ 2 ] Division of Hematology Department of MedicineUniversity of Colorado School of Medicine Aurora Colorado 80045
                Author notes
                [*] [* ] Correspondence

                Robert A. Sclafani (or) Mingxia Huang, Department of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Aurora, CO 80045. Tel: 303‐724‐3271; Fax: 303‐724‐3215; E‐mail: robert.sclafani@ 123456ucdenver.edu or mingxia.huang@ 123456ucdenver.edu

                Article
                MBO3303
                10.1002/mbo3.303
                4694146
                26450372
                844a9c39-9f2b-4db2-b817-3064b3ba2817
                © 2015 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 August 2015
                : 02 September 2015
                : 04 September 2015
                Page count
                Pages: 11
                Funding
                Funded by: National Institutes of Health
                Award ID: CA125574
                Award ID: GM35078
                Funded by: University of Colorado School of Medicine
                Categories
                Original Research
                Original Research
                Custom metadata
                2.0
                mbo3303
                December 2015
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.7.2 mode:remove_FC converted:22.12.2015

                Microbiology & Virology
                cell cycle,iron,regulon,transcriptome,yeast
                Microbiology & Virology
                cell cycle, iron, regulon, transcriptome, yeast

                Comments

                Comment on this article