DOCSLIB.ORG

BMC Genomics Biomed Central

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
BMC Genomics Biomed Central BMC Genomics BioMed Central Methodology article Open Access Comparison of gene coverage of mouse oligonucleotide microarray platforms Ricardo A Verdugo and Juan F Medrano* Address: Department of Animal Science, University of California Davis, One Shields Avenue, Davis, CA 95616-8521, USA Email: Ricardo A Verdugo - [email protected]; Juan F Medrano* - [email protected] * Corresponding author Published: 21 March 2006 Received: 24 September 2005 Accepted: 21 March 2006 BMC Genomics2006, 7:58 doi:10.1186/1471-2164-7-58 This article is available from: http://www.biomedcentral.com/1471-2164/7/58 © 2006Verdugo and Medrano; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: The increasing use of DNA microarrays for genetical genomics studies generates a need for platforms with complete coverage of the genome. We have compared the effective gene coverage in the mouse genome of different commercial and noncommercial oligonucleotide microarray platforms by performing an in-house gene annotation of probes. We only used information about probes that is available from vendors and followed a process that any researcher may take to find the gene targeted by a given probe. In order to make consistent comparisons between platforms, probes in each microarray were annotated with an Entrez Gene id and the chromosomal position for each gene was obtained from the UCSC Genome Browser Database. Gene coverage was estimated as the percentage of Entrez Genes with a unique position in the UCSC Genome database that is tested by a given microarray platform. Results: A MySQL relational database was created to store the mapping information for 25,416 mouse genes and for the probes in five microarray platforms (gene coverage level in parenthesis): Affymetrix430 2.0 (75.6%), ABI Genome Survey (81.24%), Agilent (79.33%), Codelink (78.09%), Sentrix (90.47%); and four array-ready oligosets: Sigma (47.95%), Operon v.3 (69.89%), Operon v.4 (84.03%), and MEEBO (84.03%). The differences in coverage between platforms were highly conserved across chromosomes. Differences in the number of redundant and unspecific probes were also found among arrays. The database can be queried to compare specific genomic regions using a web interface. The software used to create, update and query the database is freely available as a toolbox named ArrayGene. Conclusion: The software developed here allows researchers to create updated custom databases by using public or proprietary information on genes for any organisms. ArrayGene allows easy comparisons of gene coverage between microarray platforms for any region of the genome. The comparison presented here reveals that the commercial microarray Sentrix, which is based on the MEEBO public oligoset, showed the best mouse genome coverage currently available. We also suggest the creation of guidelines to standardize the minimum set of information that vendors should provide to allow researchers to accurately evaluate the advantages and disadvantages of using a given platform. Page 1 of 14 (page number not for citation purposes) BMC Genomics 2006, 7:58 http://www.biomedcentral.com/1471-2164/7/58 Background choosing the platform that best fits their needs. We have The wide use of DNA microarrays to query expression of developed a platform for microarray annotation that not genes has created the need for updated, consistent and only provides gene annotations for probes but also meaningful annotations on the probes included in the genomic positions for tested genes in the mouse genome. microarrays. We refer to gene annotation as a recognizable Coverage comparisons can be obtained for any genomic label or gene id identifying the gene that is targeted by a region of the last available mouse assembly build. The given probe. Gene ids should be stable, widely used and level of coverage of five whole mouse genome microarrays allow reliable associations among genomic databases. and four oligosets was compared in the present study. Several microarray annotation systems are available for Microarrays and oligosets will be referenced here by the investigators, aiming to address specific user demands. short name provided in Table 3. The results were stored in For instance, the KARMA [1] web server provides periodi- a relational database that can readily be queried for cover- cally updated gene annotations of Keck arrays [2] and age comparisons based on genome position. Figure 1 Affymetrix® GeneChips® [3], and can also annotate user- shows a flowchart diagram for the databases and methods provided lists of accession numbers for pair-wise compar- used for the annotation system and for querying gene cov- isons, even for different species. However, providing a erage comparisons. gene list is not always a straight forward process given the large heterogeneity in the format that vendors provide Results sequence identifiers for probes. For instance, one platform Number of genes in the genome can include identifiers in a Genbank header format such The total number of genes in the genome was defined as as GB|AY073000.1|AAL60663.1 and others may include the number of Entrez Genes with a unique genomic posi- different types of ids separated by commas or some other tion at the UCSC Genome Browser Database [14] (see character within a single column. In addition, different methods). A total of 198,155 mapped sequences from the sequence identifiers in several columns may be provided Known Gene, RefGene, and mRNA tracks were associated by vendors and choosing only one of them may not be the with Entrez Genes. A total of 521 genes could not be used best solution. The Resourcerer database [4] tackles this because they are located in unordered scaffolds in Build problem by pre-computing gene annotations on a more 35.1 of the mouse genome assembly. Multiple sequence exhaustive list of microarrays and oligosets for a number alignments in the genomes were found for a total of 1,766 of species [5]. This database is centered on 'tentative con- sequences. For example, the M10062 cDNA aligns with sensus' (TC) sequences which are used as gene definitions. chromosomes 1, 2, 3, 4, 6, 10, 11, 13, 15, 17, 19, X, and TCs group EST sequences that can be aligned and clus- Un_random (not chromosome assigned contigs) chro- tered in distinct groups, and these are periodically mosomes. This cDNA is identified as the Iap gene in the updated as new ESTs from GenBank become available. Entrez Gene database. This is a retrotransposon that can Functional annotations on these TCs generate the Gene be found in several chromosomes and does not have a Indices resource available from the TGI website [6]. TCs unique position. Genes like this, and other not so extreme allow for cross species comparisons through the Tentative cases, cannot be considered in region-specific coverage Orthologue Groups (TOGs) database. However, Gene comparisons and were therefore discarded. Table 2 shows Indices are not stable and cross referencing to other the number of genes that could be assigned to specific genomic databases is not easy. A different approach has position in the genome in each of the source files. The file been taken by Mattes[7] who created a set of Perl scripts Mm.gb_cid_lid in Table 1 was used to incorporate associ- that use UniGene and LocusLink as gene identifiers, pro- ations between sequences and Unigene ids in the genexref viding a more universal gene definition that can be cross table. Although we do not use Unigene annotations of referenced with other databases. Unfortunately, the recent probes to identify the targeted genes (see discussion sec- shift of NCBI from LocusLink to the Entrez Gene database tion for explanation) this allowed us to associate Entrez format [8] has limited the functionality of these scripts Gene ids with EST accession numbers, which are com- and rendered them obsolete. The DRAGON [9] database monly used in microarray genes lists. A total of 25,416 [10,11], and the DAVID [12] software [13] provide web genes could be found having a unique position in the based services of gene annotation with similar objectives. August 2005 mouse genome assembly (Build 35.1). The None of them, however, allows for chromosome or distribution of these genes in the genome is shown in Fig- genomic-region specific comparisons of gene coverage. ure 2. The objective of this study was to compare gene coverage Microarrays probe annotations from currently available whole mouse genome microar- The Resourcerer database provides gene annotations for rays for any region of the genome. We only used the infor- most of the available microarrays and oligosets for mouse mation about probes provided to researchers by vendors and other organisms [4]. However, database updates are before the purchase of a microarray for the purpose of done at four-month intervals, and in our experience, gene Page 2 of 14 (page number not for citation purposes) BMC Genomics 2006, 7:58 http://www.biomedcentral.com/1471-2164/7/58 FlowchartFigure 1 diagram for the construction and query of the ArrayGene and Aligndb databases Flowchart diagram for the construction and query of the ArrayGene and Aligndb databases. Perl scripts are used to parse input files from other databases and upload the processed information to the ArrayGene and Aligndb databases. The ma_compare CGI (Common Gateway Interface) script written in Perl is used to process queries through the web and produce online reports for gene coverage. Page 3 of 14 (page number not for citation purposes) BMC Genomics 2006, 7:58 http://www.biomedcentral.com/1471-2164/7/58 annotations change periodically and many Entrez Gene dant being the Sigma platform (1.08 probes per gene on ids in the Resourcerer annotations are obsolete.
Load more

Recommended publications
  • Subterranean Mammals Show Convergent Regression in Ocular Genes and Enhancers, Along with Adaptation to Tunneling
    RESEARCH ARTICLE Subterranean mammals show convergent regression in ocular genes and enhancers, along with adaptation to tunneling Raghavendran Partha1, Bharesh K Chauhan2,3, Zelia Ferreira1, Joseph D Robinson4, Kira Lathrop2,3, Ken K Nischal2,3, Maria Chikina1*, Nathan L Clark1* 1Department of Computational and Systems Biology, University of Pittsburgh, Pittsburgh, United States; 2UPMC Eye Center, Children’s Hospital of Pittsburgh, Pittsburgh, United States; 3Department of Ophthalmology, University of Pittsburgh School of Medicine, Pittsburgh, United States; 4Department of Molecular and Cell Biology, University of California, Berkeley, United States Abstract The underground environment imposes unique demands on life that have led subterranean species to evolve specialized traits, many of which evolved convergently. We studied convergence in evolutionary rate in subterranean mammals in order to associate phenotypic evolution with specific genetic regions. We identified a strong excess of vision- and skin-related genes that changed at accelerated rates in the subterranean environment due to relaxed constraint and adaptive evolution. We also demonstrate that ocular-specific transcriptional enhancers were convergently accelerated, whereas enhancers active outside the eye were not. Furthermore, several uncharacterized genes and regulatory sequences demonstrated convergence and thus constitute novel candidate sequences for congenital ocular disorders. The strong evidence of convergence in these species indicates that evolution in this environment is recurrent and predictable and can be used to gain insights into phenotype–genotype relationships. DOI: https://doi.org/10.7554/eLife.25884.001 *For correspondence: [email protected] (MC); [email protected] (NLC) Competing interests: The Introduction authors declare that no The subterranean habitat has been colonized by numerous animal species for its shelter and unique competing interests exist.
    [Show full text]
  • Genetic Analysis of Complex Traits in the Emerging Collaborative Cross
    Downloaded from genome.cshlp.org on October 5, 2021 - Published by Cold Spring Harbor Laboratory Press Research Genetic analysis of complex traits in the emerging Collaborative Cross David L. Aylor,1 William Valdar,1,13 Wendy Foulds-Mathes,1,13 Ryan J. Buus,1,13 Ricardo A. Verdugo,2,13 Ralph S. Baric,3,4 Martin T. Ferris,1 Jeff A. Frelinger,4 Mark Heise,1 Matt B. Frieman,4 Lisa E. Gralinski,4 Timothy A. Bell,1 John D. Didion,1 Kunjie Hua,1 Derrick L. Nehrenberg,1 Christine L. Powell,1 Jill Steigerwalt,5 Yuying Xie,1 Samir N.P. Kelada,6 Francis S. Collins,6 Ivana V. Yang,7 David A. Schwartz,7 Lisa A. Branstetter,8 Elissa J. Chesler,2 Darla R. Miller,1 Jason Spence,1 Eric Yi Liu,9 Leonard McMillan,9 Abhishek Sarkar,9 Jeremy Wang,9 Wei Wang,9 Qi Zhang,9 Karl W. Broman,10 Ron Korstanje,2 Caroline Durrant,11 Richard Mott,11 Fuad A. Iraqi,12 Daniel Pomp,1,14 David Threadgill,5,14 Fernando Pardo-Manuel de Villena,1,14 and Gary A. Churchill2,14 1Department of Genetics, University of North Carolina–Chapel Hill, Chapel Hill, North Carolina 27599, USA; 2The Jackson Laboratory, Bar Harbor, Maine 04609, USA; 3Department of Epidemiology, University of North Carolina–Chapel Hill, Chapel Hill, North Carolina 27599, USA; 4Department of Microbiology and Immunology, University of North Carolina–Chapel Hill, Chapel Hill, North Carolina 27599, USA; 5Department of Genetics, North Carolina State University, Raleigh, North Carolina 27695, USA; 6Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland
    [Show full text]
  • 15141 POMP (D2X9S) Rabbit Mab
    Revision 1 C 0 2 - t POMP (D2X9S) Rabbit mAb a e r o t S Orders: 877-616-CELL (2355) [email protected] 1 Support: 877-678-TECH (8324) 4 1 Web: [email protected] 5 www.cellsignal.com 1 # 3 Trask Lane Danvers Massachusetts 01923 USA For Research Use Only. Not For Use In Diagnostic Procedures. Applications: Reactivity: Sensitivity: MW (kDa): Source/Isotype: UniProt ID: Entrez-Gene Id: WB, IP H M R Mk Endogenous 16 Rabbit IgG Q9Y244 51371 Product Usage Information immunoproteasomes, and that the assembly focal point resides at the endoplasmic reticulum (6-8). A single nucleotide deletion in the 5' UTR of POMP results in altered Application Dilution epidermal POMP distribution and the autosomal recessive skin disorder known as KLICK syndrome (9). Western Blotting 1:1000 1. Finley, D. (2009) Annu Rev Biochem 78, 477-513. Immunoprecipitation 1:200 2. Lee, M.J. et al. (2011) Mol Cell Proteomics 10, R110.003871. 3. Griffin, T.A. et al. (2000) Mol Cell Biol Res Commun 3, 212-7. 4. Witt, E. et al. (2000) J Mol Biol 301, 1-9. Storage 5. Ramos, P.C. et al. (1998) Cell 92, 489-99. Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% 6. Fricke, B. et al. (2007) EMBO Rep 8, 1170-5. glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody. 7. Heink, S. et al. (2005) Proc Natl Acad Sci U S A 102, 9241-6. 8. Heink, S.
    [Show full text]
  • Downloaded Per Proteome Cohort Via the Web- Site Links of Table 1, Also Providing Information on the Deposited Spectral Datasets
    www.nature.com/scientificreports OPEN Assessment of a complete and classifed platelet proteome from genome‑wide transcripts of human platelets and megakaryocytes covering platelet functions Jingnan Huang1,2*, Frauke Swieringa1,2,9, Fiorella A. Solari2,9, Isabella Provenzale1, Luigi Grassi3, Ilaria De Simone1, Constance C. F. M. J. Baaten1,4, Rachel Cavill5, Albert Sickmann2,6,7,9, Mattia Frontini3,8,9 & Johan W. M. Heemskerk1,9* Novel platelet and megakaryocyte transcriptome analysis allows prediction of the full or theoretical proteome of a representative human platelet. Here, we integrated the established platelet proteomes from six cohorts of healthy subjects, encompassing 5.2 k proteins, with two novel genome‑wide transcriptomes (57.8 k mRNAs). For 14.8 k protein‑coding transcripts, we assigned the proteins to 21 UniProt‑based classes, based on their preferential intracellular localization and presumed function. This classifed transcriptome‑proteome profle of platelets revealed: (i) Absence of 37.2 k genome‑ wide transcripts. (ii) High quantitative similarity of platelet and megakaryocyte transcriptomes (R = 0.75) for 14.8 k protein‑coding genes, but not for 3.8 k RNA genes or 1.9 k pseudogenes (R = 0.43–0.54), suggesting redistribution of mRNAs upon platelet shedding from megakaryocytes. (iii) Copy numbers of 3.5 k proteins that were restricted in size by the corresponding transcript levels (iv) Near complete coverage of identifed proteins in the relevant transcriptome (log2fpkm > 0.20) except for plasma‑derived secretory proteins, pointing to adhesion and uptake of such proteins. (v) Underrepresentation in the identifed proteome of nuclear‑related, membrane and signaling proteins, as well proteins with low‑level transcripts.
    [Show full text]
  • Download.Cse.Ucsc.Edu/Goldenpath/ Knowngene Mm7/Database/ Refgene All Mrna Knowntoensembl
    BMC Genomics BioMed Central Methodology article Open Access Comparison of gene coverage of mouse oligonucleotide microarray platforms Ricardo A Verdugo and Juan F Medrano* Address: Department of Animal Science, University of California Davis, One Shields Avenue, Davis, CA 95616-8521, USA Email: Ricardo A Verdugo - [email protected]; Juan F Medrano* - [email protected] * Corresponding author Published: 21 March 2006 Received: 24 September 2005 Accepted: 21 March 2006 BMC Genomics2006, 7:58 doi:10.1186/1471-2164-7-58 This article is available from: http://www.biomedcentral.com/1471-2164/7/58 © 2006Verdugo and Medrano; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: The increasing use of DNA microarrays for genetical genomics studies generates a need for platforms with complete coverage of the genome. We have compared the effective gene coverage in the mouse genome of different commercial and noncommercial oligonucleotide microarray platforms by performing an in-house gene annotation of probes. We only used information about probes that is available from vendors and followed a process that any researcher may take to find the gene targeted by a given probe. In order to make consistent comparisons between platforms, probes in each microarray were annotated with an Entrez Gene id and the chromosomal position for each gene was obtained from the UCSC Genome Browser Database. Gene coverage was estimated as the percentage of Entrez Genes with a unique position in the UCSC Genome database that is tested by a given microarray platform.
    [Show full text]
  • Genetic Amplification of the NOTCH Modulator LNX2 Upregulates The
    Cancer Tumor and Stem Cell Biology Research Genetic Amplification of the NOTCH Modulator LNX2 Upregulates the WNT/b-Catenin Pathway in Colorectal Cancer Jordi Camps1, Jason J. Pitt2, Georg Emons1,3, Amanda B. Hummon1, Chanelle M. Case1, Marian Grade1,3, Tamara L. Jones2, Quang T. Nguyen1, B. Michael Ghadimi3, Tim Beissbarth3, Michael J. Difilippantonio1, Natasha J. Caplen2, and Thomas Ried1 Abstract Chromosomal copy number alterations (aneuploidy) define the genomic landscape of most cancer cells, but identification of the oncogenic drivers behind these imbalances remains an unfinished task. In this study, we conducted a systematic analysis of colorectal carcinomas that integrated genomic copy number changes and gene expression profiles. This analysis revealed 44 highly overexpressed genes mapping to localized amplicons on chromosome 13, gains of which occur often in colorectal cancers (CRC). RNA interference (RNAi)–mediated silencing identified eight candidates whose loss-of-function reduced cell viability 20% or more in CRC cell lines. The functional space of the genes NUPL1, LNX2, POLR1D, POMP, SLC7A1, DIS3, KLF5, and GPR180 was established by global expression profiling after RNAi exposure. One candidate, LNX2, not previously known as an oncogene, was involved in regulating NOTCH signaling. Silencing LNX2 reduced NOTCH levels but also downregulated the transcription factor TCF7L2 and markedly reduced WNT signaling. LNX2 overexpression and chromosome 13 amplification therefore constitutively activates the WNT pathway, offering evidence of an aberrant NOTCH–WNT axis in CRC. Cancer Res; 73(6); 1–11. Ó2012 AACR. Introduction band or less) or they affect entire chromosome arms or Colorectal cancer (CRC) has an annual incidence of some chromosomes, most commonly resulting in low level gains or 150,000 new cases and a mortality of more than 50,000 in the losses.
    [Show full text]
  • Quantitative Trait Loci for Energy Balance Traits in an Advanced Intercross Line Derived from Mice Divergently Selected for Heat Loss Larry J
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Papers and Publications in Animal Science Animal Science Department 2014 Quantitative trait loci for energy balance traits in an advanced intercross line derived from mice divergently selected for heat loss Larry J. Leamy University of North Carolina at Charlotte, [email protected] Kari Elo University of Helsinki Merlyn K. Nielsen University of Nebraska - Lincoln, [email protected] Stephanie R. Thorn University of Colorado William Valdar University of North Carolina at Chapel Hill See next page for additional authors Follow this and additional works at: https://digitalcommons.unl.edu/animalscifacpub Part of the Genetics and Genomics Commons, and the Meat Science Commons Leamy, Larry J.; Elo, Kari; Nielsen, Merlyn K.; Thorn, Stephanie R.; Valdar, William; and Pomp, Daniel, "Quantitative trait loci for energy balance traits in an advanced intercross line derived from mice divergently selected for heat loss" (2014). Faculty Papers and Publications in Animal Science. 1031. https://digitalcommons.unl.edu/animalscifacpub/1031 This Article is brought to you for free and open access by the Animal Science Department at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Papers and Publications in Animal Science by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Authors Larry J. Leamy, Kari Elo, Merlyn K. Nielsen, Stephanie R. Thorn, William Valdar, and Daniel Pomp This article is available at DigitalCommons@University of Nebraska - Lincoln: https://digitalcommons.unl.edu/animalscifacpub/ 1031 Quantitative trait loci for energy balance traits in an advanced intercross line derived from mice divergently selected for heat loss Larry J.
    [Show full text]
  • Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
    Table S1. 103 ferroptosis-related genes retrieved from the GeneCards. Gene Symbol Description Category GPX4 Glutathione Peroxidase 4 Protein Coding AIFM2 Apoptosis Inducing Factor Mitochondria Associated 2 Protein Coding TP53 Tumor Protein P53 Protein Coding ACSL4 Acyl-CoA Synthetase Long Chain Family Member 4 Protein Coding SLC7A11 Solute Carrier Family 7 Member 11 Protein Coding VDAC2 Voltage Dependent Anion Channel 2 Protein Coding VDAC3 Voltage Dependent Anion Channel 3 Protein Coding ATG5 Autophagy Related 5 Protein Coding ATG7 Autophagy Related 7 Protein Coding NCOA4 Nuclear Receptor Coactivator 4 Protein Coding HMOX1 Heme Oxygenase 1 Protein Coding SLC3A2 Solute Carrier Family 3 Member 2 Protein Coding ALOX15 Arachidonate 15-Lipoxygenase Protein Coding BECN1 Beclin 1 Protein Coding PRKAA1 Protein Kinase AMP-Activated Catalytic Subunit Alpha 1 Protein Coding SAT1 Spermidine/Spermine N1-Acetyltransferase 1 Protein Coding NF2 Neurofibromin 2 Protein Coding YAP1 Yes1 Associated Transcriptional Regulator Protein Coding FTH1 Ferritin Heavy Chain 1 Protein Coding TF Transferrin Protein Coding TFRC Transferrin Receptor Protein Coding FTL Ferritin Light Chain Protein Coding CYBB Cytochrome B-245 Beta Chain Protein Coding GSS Glutathione Synthetase Protein Coding CP Ceruloplasmin Protein Coding PRNP Prion Protein Protein Coding SLC11A2 Solute Carrier Family 11 Member 2 Protein Coding SLC40A1 Solute Carrier Family 40 Member 1 Protein Coding STEAP3 STEAP3 Metalloreductase Protein Coding ACSL1 Acyl-CoA Synthetase Long Chain Family Member 1 Protein
    [Show full text]
  • Gene Expression Analysis in LLC-PK1 Renal Tubular Cells by Atrial Natriuretic Peptide (ANP): Correlation of Homologous Human Genes with Renal Response
    Journal of Biomedical Science DOI 10.1007/s11373-007-9152-8 Gene expression analysis in LLC-PK1 renal tubular cells by atrial natriuretic peptide (ANP): correlation of homologous human genes with renal response Rosa Huang Liu1, Sun-Long Cheng2, Kwo-Chang Ueng3, Der-Jinn Wu4, Shui-Tein Chen5,6, Supachok Sinchaikul5 & Tsung-Han Lee1,* 1Department of Life Sciences, National Chung Hsing University, 250, Kuo-Kuang Road, Taichung, 40227, Taiwan; 2Department of Surgical Medicine, Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan; 3Division of Cardiology and Cardiovascular Surgery, Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan; 4Department of Internal Medicine, Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan; 5Institute of Biological Chemistry and Genomics Research Center, Academia Sinica, Taipei, Taiwan; 6Institute of Biochemical Sciences, College of Life Science, National Taiwan Uni- versity, Taipei, Taiwan Received 7 August 2006; accepted 12 January 2007 Ó 2007 National Science Council, Taipei Key words: atrial natriuretic peptide (ANP), LLC-PK1 cells, gene expression, microarray Summary We used human DNA microarray to explore the differential gene expression profiling of atrial natriuretic peptide (ANP)-stimulated renal tubular epithelial kidney cells (LLC-PK1) in order to understand the bio- logical effect of ANP on renal kidney cellÕs response. Gene expression profiling revealed 807 differentially expressed genes, consisting of 483 up-regulated and 324 down-regulated genes. The bioinformatics tool was used to gain a better understanding of differentially expressed genes in porcine genome homologous with human genome and to search the gene ontology and category classification, such as cellular component, molecular function and biological process.
    [Show full text]
  • Human Genome Project Left 8 Percent of Our DNA Unexplored
    6/15/2021 The Human Genome Is—Finally!—Complete - The Atlantic SCIENCE e Human Genome Is—Finally!— Complete e Human Genome Project left 8 percent of our DNA unexplored. Now, for the ërst time, those enigmatic regions have been revealed. By Sarah Zhang Olympia Valla / Getty; Nurk et al.; Katie Martin / The Atlantic JUNE 11, 2021 SHARE https://www.theatlantic.com/science/archive/2021/06/the-human-genome-is-finally-complete/619172/ 1/6 6/15/2021 The Human Genome Is—Finally!—Complete - The Atlantic When the human genome was ërst deemed “complete” in 2000, the news was met with great international fanfare. e two rival groups vying to ënish the genome ërst —one a large government-led consortium, the other an underdog private company— agreed to declare joint success. ey shook hands at the White House. Bill Clinton presided. Tony Blair beamed in from London. “We are standing at an extraordinary moment in scientiëc history,” one prominent scientist declared when those genomes were published. “It’s as though we have climbed to the top of the Himalayas.” But actually, the human genome was not complete. Neither group had reached the real summit. As even the contemporary coverage acknowledged, that version was more of a rough draft, riddled with long stretches where the DNA sequence was still fuzzy or missing. e private company soon pivoted and ended its human-genome project, though scientists with the public consortium soldiered on. In 2003, with less glitz but still plenty of headlines, the human genome was declared complete once again. But actually, the human genome was still not complete.
    [Show full text]
  • CD44 Expression Predicts Local Recurrence After Radiotherapy in Larynx Cancer
    Published OnlineFirst September 13, 2010; DOI: 10.1158/1078-0432.CCR-10-0799 Predictive Biomarkers and Personalized Medicine Clinical Cancer See commentary p. 5091 Research CD44 Expression Predicts Local Recurrence after Radiotherapy in Larynx Cancer Monique C. de Jong1,2, Jimmy Pramana1,3, Jacqueline E. van der Wal10, Martin Lacko5, Carine J. Peutz-Kootstra6, Jos M. de Jong7, Robert P. Takes8, Johannes H. Kaanders9, Bernard F. van der Laan11, Jasper Wachters10,11, Jeroen C. Jansen12, Coen R. Rasch2, Marie-Louise F. van Velthuysen4, Reidar Grénman13, Frank J. Hoebers2, Ed Schuuring10, Michiel W. van den Brekel3, and Adrian C. Begg1 Abstract Purpose: To find molecular markers from expression profiling data to predict recurrence of laryngeal cancer after radiotherapy. Experimental Design: We generated gene expression data on pre-treatment biopsies from 52 larynx cancer patients. Patients developing a local recurrence were matched for T-stage, subsite, treatment, gen- der and age with non-recurrence patients. Candidate genes were then tested by immunohistochemistry on tumor material from a second series of 76 patients. Both series comprised early stage cancer treated with radiotherapy alone. Finally, gene expression data of eight larynx cancer cell lines with known radiosen- sitivity were analyzed. Results: Nineteen patients with a local recurrence were matched with 33 controls. Gene sets for hyp- oxia, proliferation and intrinsic radiosensitivity did not correlate with recurrence, whereas expression of the putative stem cell marker CD44 did. In a supervised analysis, probes for all three splice variants of CD44 on the array appeared in the top 10 most significantly correlated with local recurrence. Immuno- histochemical analysis of CD44 expression on the independent validation series confirmed CD44's pre- dictive potential.
    [Show full text]
  • NRF1 and NRF3 Complementarily Maintain a Basal Proteasome Activity in Cancer Cells Through CPEB3-Mediated Translational Repressi
    bioRxiv preprint doi: https://doi.org/10.1101/2020.01.10.902718; this version posted January 11, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. 1 NRF1 and NRF3 complementarily maintain a basal proteasome activity in cancer cells 2 through CPEB3-mediated translational repression 3 4 Running title: NRF3-CPEB3-NRF1 axis for proteasome regulation 5 6 Tsuyoshi Waku1 † , Hiroyuki Katayama2 † , Miyako Hiraoka2, Atsushi Hatanaka2, 3, Nanami 7 Nakamura2, Yuya Tanaka1, Natsuko Tamura2, Akira Watanabe4, Akira Kobayashi1,2* 8 9 †Equal contribution 10 11 1Laboratory for Genetic Code, Department of Medical Life Systems, Faculty of Life and Medical 12 Sciences, Doshisha University, Kyotanabe, Kyoto, Japan 13 2Laboratory for Genetic Code, Graduate School of Life and Medical Sciences, Doshisha 14 University, Kyotanabe, Kyoto, Japan 15 3Research Fellow of Japan Society for the Promotion of Science, Tokyo, Japan 16 4Department of Life Science Frontiers, Center for iPS Cell Research and Application, Kyoto 17 University, Kyoto, Japan 18 19 20 21 22 23 *To whom correspondence should be addressed: 24 Akira Kobayashi 25 1-3 Tatara Miyakodani, Kyotanabe 610-0394, Japan 26 Phone: +81-774-65-6273 27 Fax: +81-774-65-6274 28 E-mail: [email protected] 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.01.10.902718; this version posted January 11, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity.
    [Show full text]