Supp Tables Feb 2008

Total Page:16

File Type:pdf, Size:1020Kb

Supp Tables Feb 2008 Supplementary Table 1. (a) Basal alkylation sensitivity associated gene set (BASA) sorted by correlation (page 1 of 2) Present in Gene Symbol Gene Title Representative Public ID Probeset ID R (train) R (all) % accuracy Network MGMT O-6-methylguanine-DNA methyltransferase NM_002412 204880_at 0.95 0.74 69 Yes C21orf56 chromosome 21 open reading frame 56 AL136871 223360_at 0.86 0.54 56 No NQO2 NAD(P)H dehydrogenase, quinone 2 NM_000904 203814_s_at -0.71 -0.53 69 No glycerol-3-phosphate dehydrogenase 2 GPD2 (mitochondrial) U36310 210007_s_at -0.72 -0.59 63 Yes RAD54B RAD54 homolog B (S. cerevisiae) NM_012415 219494_at -0.72 -0.66 63 Yes PIAS2 protein inhibitor of activated STAT, 2 AF361054 1555514_a_at -0.73 -0.58 69 No FLJ12442 hypothetical protein FLJ12442 NM_022908 218051_s_at -0.73 -0.53 69 No TM4SF12 transmembrane 4 superfamily member 12 NM_012338 219274_at -0.76 -0.58 63 No LRRK1 leucine-rich repeat kinase 1 AW792857 1565627_a_at -0.76 -0.53 81 No ARSB arylsulfatase B AW168942 232197_x_at -0.77 -0.52 75 No PPP2R1B protein phosphatase 2 (formerly 2A) T79584 202883_s_at -0.78 -0.58 56 Yes MSC musculin (activated B-cell factor-1) AF060154 209928_s_at -0.78 -0.55 69 Yes LOC283130 hypothetical protein LOC283130 AI336233 236436_at -0.79 -0.58 69 No LAMC1 laminin, gamma 1 (formerly LAMB2) NM_002293 200771_at -0.79 -0.69 75 Yes FLJ12886 hypothetical protein FLJ12886 NM_019108 221335_x_at -0.81 -0.59 75 No discoidin, CUB and LCCL domain containing DCBLD1 1 NM_173674 1553768_a_at -0.81 -0.53 75 No CMIP c-Maf-inducing protein AI363061 224992_s_at -0.81 -0.54 63 Yes --- --- AI825302 238700_at -0.82 -0.64 63 No platelet/endothelial cell adhesion molecule PECAM1 (CD31 antigen) M37780 208983_s_at -0.82 -0.62 63 Yes FLJ32942 hypothetical protein FLJ32942 BG150433 227711_at -0.82 -0.61 75 No LOC284801 hypothetical protein LOC284801 AL531683 225762_x_at -0.83 -0.62 63 No guanine nucleotide binding protein (G GNB5 protein), beta 5 NM_006578 207124_s_at -0.83 -0.71 81 Yes sarcoglycan, beta (43kDa dystrophin- SGCB associated glycoprotein) U29586 205120_s_at -0.83 -0.68 63 Yes SFXN2 sideroflexin 2 AL530504 227560_at -0.83 -0.54 56 No SYPL synaptophysin-like protein AI768845 201259_s_at -0.84 -0.58 69 No DTNBP1 dystrobrevin binding protein 1 AF061734 223446_s_at -0.84 -0.68 75 Yes LOC203069 hypothetical protein LOC203069 AI081543 212866_at -0.84 -0.74 75 No MESDC2 mesoderm development candidate 2 AK026606 224675_at -0.85 -0.65 63 No FIGNL1 fidgetin-like 1 NM_022116 1552921_a_at -0.85 -0.71 69 Yes PHYH phytanoyl-CoA hydroxylase (Refsum disease) NM_006214 203335_at -0.85 -0.61 75 Yes Supplementary Table 1. (a) Basal alkylation sensitivity associated gene set (BASA) sorted by correlation (page 2 of 2) Present in Gene Symbol Gene Title Representative Public ID Probeset ID R (train) R (all) % accuracy Network TM4SF7 transmembrane 4 superfamily member 7 BC000389 209263_x_at -0.85 -0.68 75 No echinoderm microtubule associated protein EML4 like 4 NM_019063 220386_s_at -0.85 -0.60 81 No CKLFSF3 chemokine-like factor super family 3 AY166714 1555705_a_at -0.86 -0.58 69 No MGC45731 hypothetical protein MGC45731 AW003092 227080_at -0.86 -0.58 63 No phosphoinositide-3-kinase, regulatory PIK3R1 subunit, polypeptide 1 (p85 alpha) AI680192 212239_at -0.87 -0.76 63 No MAGEF1 melanoma antigen, family F, 1 NM_022149 218176_at -0.88 -0.72 81 Yes TMEM14A transmembrane protein 14A NM_014051 218477_at -0.88 -0.70 63 No ANKRD9 ankyrin repeat domain 9 AW194999 230972_at -0.90 -0.67 75 No MGC11266 hypothetical protein MGC11266 BE326728 226118_at -0.91 -0.70 63 Yes DTYMK deoxythymidylate kinase (thymidylate kinase) NM_012145 203270_at -0.91 -0.58 56 No CANP cancer-associated nucleoprotein AA960844 1557128_at -0.91 -0.50 63 No --- --- BE467688 231259_s_at -0.92 -0.52 56 No H2AFV H2A histone family, member V BF343852 212206_s_at -0.92 -0.70 69 No NET1 neuroepithelial cell transforming gene 1 NM_005863 201830_s_at -0.92 -0.58 56 Yes TSAP6 dudulin 2 NM_018234 218424_s_at -0.92 -0.70 75 Yes --- --- AA227879 235919_at -0.93 -0.58 56 No CKLF chemokine-like factor NM_016951 219161_s_at -0.94 -0.62 75 No MUTYH mutY homolog (E. coli) NM_012222 207727_s_at -0.97 -0.76 69 Yes ALL 94 Supplementary Table 1. (b) Basal alkylation sensitivity associated gene set (BASA) sorted by gene (page 1 of 2) Present in Gene Symbol Gene Title Representative Public ID Probeset ID R (train) R (all) % accuracy Network ANKRD9 ankyrin repeat domain 9 AW194999 230972_at -0.90 -0.67 75 No ARSB arylsulfatase B AW168942 232197_x_at -0.77 -0.52 75 No C21orf56 chromosome 21 open reading frame 56 AL136871 223360_at 0.86 0.54 56 No CANP cancer-associated nucleoprotein AA960844 1557128_at -0.91 -0.50 63 No CKLF chemokine-like factor NM_016951 219161_s_at -0.94 -0.62 75 No CKLFSF3 chemokine-like factor super family 3 AY166714 1555705_a_at -0.86 -0.58 69 No CMIP c-Maf-inducing protein AI363061 224992_s_at -0.81 -0.54 63 Yes discoidin, CUB and LCCL domain containing DCBLD1 1 NM_173674 1553768_a_at -0.81 -0.53 75 No DTNBP1 dystrobrevin binding protein 1 AF061734 223446_s_at -0.84 -0.68 75 Yes DTYMK deoxythymidylate kinase (thymidylate kinase) NM_012145 203270_at -0.91 -0.58 56 No echinoderm microtubule associated protein EML4 like 4 NM_019063 220386_s_at -0.85 -0.60 81 No FIGNL1 fidgetin-like 1 NM_022116 1552921_a_at -0.85 -0.71 69 Yes FLJ12442 hypothetical protein FLJ12442 NM_022908 218051_s_at -0.73 -0.53 69 No FLJ12886 hypothetical protein FLJ12886 NM_019108 221335_x_at -0.81 -0.59 75 No FLJ32942 hypothetical protein FLJ32942 BG150433 227711_at -0.82 -0.61 75 No guanine nucleotide binding protein (G GNB5 protein), beta 5 NM_006578 207124_s_at -0.83 -0.71 81 Yes glycerol-3-phosphate dehydrogenase 2 GPD2 (mitochondrial) U36310 210007_s_at -0.72 -0.59 63 Yes H2AFV H2A histone family, member V BF343852 212206_s_at -0.92 -0.70 69 No LAMC1 laminin, gamma 1 (formerly LAMB2) NM_002293 200771_at -0.79 -0.69 75 Yes LOC203069 hypothetical protein LOC203069 AI081543 212866_at -0.84 -0.74 75 No LOC283130 hypothetical protein LOC283130 AI336233 236436_at -0.79 -0.58 69 No LOC284801 hypothetical protein LOC284801 AL531683 225762_x_at -0.83 -0.62 63 No LRRK1 leucine-rich repeat kinase 1 AW792857 1565627_a_at -0.76 -0.53 81 No MAGEF1 melanoma antigen, family F, 1 NM_022149 218176_at -0.88 -0.72 81 Yes MESDC2 mesoderm development candidate 2 AK026606 224675_at -0.85 -0.65 63 No MGC11266 hypothetical protein MGC11266 BE326728 226118_at -0.91 -0.70 63 Yes MGC45731 hypothetical protein MGC45731 AW003092 227080_at -0.86 -0.58 63 No MGMT O-6-methylguanine-DNA methyltransferase NM_002412 204880_at 0.95 0.74 69 Yes MSC musculin (activated B-cell factor-1) AF060154 209928_s_at -0.78 -0.55 69 Yes MUTYH mutY homolog (E. coli) NM_012222 207727_s_at -0.97 -0.76 69 Yes Supplementary Table 1. (b) Basal alkylation sensitivity associated gene set (BASA) sorted by gene (page 2 of 2) Present in Gene Symbol Gene Title Representative Public ID Probeset ID R (train) R (all) % accuracy Network NET1 neuroepithelial cell transforming gene 1 NM_005863 201830_s_at -0.92 -0.58 56 Yes NQO2 NAD(P)H dehydrogenase, quinone 2 NM_000904 203814_s_at -0.71 -0.53 69 No platelet/endothelial cell adhesion molecule PECAM1 (CD31 antigen) M37780 208983_s_at -0.82 -0.62 63 Yes PHYH phytanoyl-CoA hydroxylase (Refsum disease) NM_006214 203335_at -0.85 -0.61 75 Yes PIAS2 protein inhibitor of activated STAT, 2 AF361054 1555514_a_at -0.73 -0.58 69 No phosphoinositide-3-kinase, regulatory PIK3R1 subunit, polypeptide 1 (p85 alpha) AI680192 212239_at -0.87 -0.76 63 No protein phosphatase 2 (formerly 2A), PPP2R1B regulatory subunit A (PR 65), beta isoform T79584 202883_s_at -0.78 -0.58 56 Yes RAD54B RAD54 homolog B (S. cerevisiae) NM_012415 219494_at -0.72 -0.66 63 Yes SFXN2 sideroflexin 2 AL530504 227560_at -0.83 -0.54 56 No sarcoglycan, beta (43kDa dystrophin- SGCB associated glycoprotein) U29586 205120_s_at -0.83 -0.68 63 Yes SYPL synaptophysin-like protein AI768845 201259_s_at -0.84 -0.58 69 No TM4SF12 transmembrane 4 superfamily member 12 NM_012338 219274_at -0.76 -0.58 63 No TM4SF7 transmembrane 4 superfamily member 7 BC000389 209263_x_at -0.85 -0.68 75 No TMEM14A transmembrane protein 14A NM_014051 218477_at -0.88 -0.70 63 No TSAP6 dudulin 2 NM_018234 218424_s_at -0.92 -0.70 75 Yes --- --- AI825302 238700_at -0.82 -0.64 63 No --- --- AA227879 235919_at -0.93 -0.58 56 No --- --- BE467688 231259_s_at -0.92 -0.52 56 No ALL 94 Supplementary Table 2. (a) Treated Ratio alkylation sensitivity associated gene set (TRASA) sorted by correlation (page 1 of 2) Gene Symbol Gene Title Representative Public ID Probeset ID R (train) R (all) low density lipoprotein receptor (familial LDLR hypercholesterolemia) NM_000527 202068_s_at 0.98 0.85 BCL2/adenovirus E1B 19kDa interacting BNIP3 protein 3 U15174 201848_s_at 0.94 0.86 --- --- AI375915 1555852_at 0.93 0.73 ZNF395 zinc finger protein 395 /// F-box protein 16 BC001237 223216_x_at 0.93 0.82 SCD stearoyl-CoA desaturase (delta-9-desaturase) AB032261 200832_s_at 0.93 0.76 histone 2, H2aa /// similar to Histone H2A.o HIST2H2AA (H2A/o) (H2A.2) (H2a-615) /// histone H2A/r NM_003516 218280_x_at 0.92 0.67 CTA-126B4.3 CGI-96 protein AL022316 202937_x_at 0.92 0.48 ING2 inhibitor of growth family, member 2 NM_001564 205981_s_at 0.91 0.75 PRO1843 hypothetical protein PRO1843 NM_018507 219599_at 0.90 0.38 --- --- AK026764 226348_at 0.89 0.72 C10orf75 Chromosome 10 open reading frame 75 AU151788 232230_at 0.88 0.68 LOC440731 hypothetical LOC440731 AI286239 237563_s_at 0.88 0.50 BCL2/adenovirus E1B 19kDa interacting BNIP3L protein 3-like /// BCL2/adenovirus
Recommended publications
  • The Rise and Fall of the Bovine Corpus Luteum
    University of Nebraska Medical Center DigitalCommons@UNMC Theses & Dissertations Graduate Studies Spring 5-6-2017 The Rise and Fall of the Bovine Corpus Luteum Heather Talbott University of Nebraska Medical Center Follow this and additional works at: https://digitalcommons.unmc.edu/etd Part of the Biochemistry Commons, Molecular Biology Commons, and the Obstetrics and Gynecology Commons Recommended Citation Talbott, Heather, "The Rise and Fall of the Bovine Corpus Luteum" (2017). Theses & Dissertations. 207. https://digitalcommons.unmc.edu/etd/207 This Dissertation is brought to you for free and open access by the Graduate Studies at DigitalCommons@UNMC. It has been accepted for inclusion in Theses & Dissertations by an authorized administrator of DigitalCommons@UNMC. For more information, please contact [email protected]. THE RISE AND FALL OF THE BOVINE CORPUS LUTEUM by Heather Talbott A DISSERTATION Presented to the Faculty of the University of Nebraska Graduate College in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy Biochemistry and Molecular Biology Graduate Program Under the Supervision of Professor John S. Davis University of Nebraska Medical Center Omaha, Nebraska May, 2017 Supervisory Committee: Carol A. Casey, Ph.D. Andrea S. Cupp, Ph.D. Parmender P. Mehta, Ph.D. Justin L. Mott, Ph.D. i ACKNOWLEDGEMENTS This dissertation was supported by the Agriculture and Food Research Initiative from the USDA National Institute of Food and Agriculture (NIFA) Pre-doctoral award; University of Nebraska Medical Center Graduate Student Assistantship; University of Nebraska Medical Center Exceptional Incoming Graduate Student Award; the VA Nebraska-Western Iowa Health Care System Department of Veterans Affairs; and The Olson Center for Women’s Health, Department of Obstetrics and Gynecology, Nebraska Medical Center.
    [Show full text]
  • SPATA33 Localizes Calcineurin to the Mitochondria and Regulates Sperm Motility in Mice
    SPATA33 localizes calcineurin to the mitochondria and regulates sperm motility in mice Haruhiko Miyataa, Seiya Ouraa,b, Akane Morohoshia,c, Keisuke Shimadaa, Daisuke Mashikoa,1, Yuki Oyamaa,b, Yuki Kanedaa,b, Takafumi Matsumuraa,2, Ferheen Abbasia,3, and Masahito Ikawaa,b,c,d,4 aResearch Institute for Microbial Diseases, Osaka University, Osaka 5650871, Japan; bGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 5650871, Japan; cGraduate School of Medicine, Osaka University, Osaka 5650871, Japan; and dThe Institute of Medical Science, The University of Tokyo, Tokyo 1088639, Japan Edited by Mariana F. Wolfner, Cornell University, Ithaca, NY, and approved July 27, 2021 (received for review April 8, 2021) Calcineurin is a calcium-dependent phosphatase that plays roles in calcineurin can be a target for reversible and rapidly acting male a variety of biological processes including immune responses. In sper- contraceptives (5). However, it is challenging to develop molecules matozoa, there is a testis-enriched calcineurin composed of PPP3CC and that specifically inhibit sperm calcineurin and not somatic calci- PPP3R2 (sperm calcineurin) that is essential for sperm motility and male neurin because of sequence similarities (82% amino acid identity fertility. Because sperm calcineurin has been proposed as a target for between human PPP3CA and PPP3CC and 85% amino acid reversible male contraceptives, identifying proteins that interact with identity between human PPP3R1 and PPP3R2). Therefore, identi- sperm calcineurin widens the choice for developing specific inhibitors. fying proteins that interact with sperm calcineurin widens the choice Here, by screening the calcineurin-interacting PxIxIT consensus motif of inhibitors that target the sperm calcineurin pathway. in silico and analyzing the function of candidate proteins through the The PxIxIT motif is a conserved sequence found in generation of gene-modified mice, we discovered that SPATA33 inter- calcineurin-binding proteins (8, 9).
    [Show full text]
  • Genetic Basis of Simple and Complex Traits with Relevance to Avian Evolution
    Genetic basis of simple and complex traits with relevance to avian evolution Małgorzata Anna Gazda Doctoral Program in Biodiversity, Genetics and Evolution D Faculdade de Ciências da Universidade do Porto 2019 Supervisor Miguel Jorge Pinto Carneiro, Auxiliary Researcher, CIBIO/InBIO, Laboratório Associado, Universidade do Porto Co-supervisor Ricardo Lopes, CIBIO/InBIO Leif Andersson, Uppsala University FCUP Genetic basis of avian traits Nota Previa Na elaboração desta tese, e nos termos do número 2 do Artigo 4º do Regulamento Geral dos Terceiros Ciclos de Estudos da Universidade do Porto e do Artigo 31º do D.L.74/2006, de 24 de Março, com a nova redação introduzida pelo D.L. 230/2009, de 14 de Setembro, foi efetuado o aproveitamento total de um conjunto coerente de trabalhos de investigação já publicados ou submetidos para publicação em revistas internacionais indexadas e com arbitragem científica, os quais integram alguns dos capítulos da presente tese. Tendo em conta que os referidos trabalhos foram realizados com a colaboração de outros autores, o candidato esclarece que, em todos eles, participou ativamente na sua conceção, na obtenção, análise e discussão de resultados, bem como na elaboração da sua forma publicada. Este trabalho foi apoiado pela Fundação para a Ciência e Tecnologia (FCT) através da atribuição de uma bolsa de doutoramento (PD/BD/114042/2015) no âmbito do programa doutoral em Biodiversidade, Genética e Evolução (BIODIV). 2 FCUP Genetic basis of avian traits Acknowledgements Firstly, I would like to thank to my all supervisors Miguel Carneiro, Ricardo Lopes and Leif Andersson, for the demanding task of supervising myself last four years.
    [Show full text]
  • Single Nucleotide Polymorphisms Within Calcineurin-Encoding Genes
    Annals of Applied Sport Science, vol. 4, no. 2, pp. 01-08, Summer 2016 DOI: 10.18869/acadpub.aassjournal.4.2.1 Original Article www.aassjournal.com www.AESAsport.com ISSN (Online): 2322 – 4479 Received: 06/03/2016 ISSN (Print): 2476–4981 Accepted: 26/06/2016 Single Nucleotide Polymorphisms within Calcineurin-Encoding Genes are Associated with Response to Aerobic Training in Han Chinese Males 1Rong-mei Xu, 2Tao Lu, 2Lingxian Yan, 1Qinghua Song* 1The Center of Physical Health, Henan Polytechnic University, Jiaozuo 454000, Henan Province, China. 2 The Lab of Human Body Science, Henan Polytechnic University, Jiaozuo 454000, Henan Province, China. ABSTRACT Calcineurin, which functions in calcium signaling, is expressed in skeletal and cardiac muscle and has been linked to sensitivity to muscle strength training. It is also proposed to contribute to individual aerobic endurance. To investigate the relationship between calcineurin-encoding genes and aerobic endurance traits, 126 young-adult Han Chinese males were enrolled in an aerobic exercise training study. Participants were genotyped for polymorphisms within the 5 genes (PPP3CA, PPP3CB, PPP3CC, PPP3R1 and PPP3R2) encoding calcineurin using restriction fragment length polymorphism polymerase chain reaction (PCR-RFLP) or matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS). Participants underwent 18 weeks of aerobic exercise training (running). Before and after the training period, maximal oxygen uptake (VO2max) and 12 km/h running economy were measured. Statistical analyses were performed using chi-square test and analysis of variance. The baseline value of VO2max was significantly associated with rs3804423 and rs2850965 loci in the PPP3CA gene (P<0.05).
    [Show full text]
  • A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
    Page 1 of 781 Diabetes A Computational Approach for Defining a Signature of β-Cell Golgi Stress in Diabetes Mellitus Robert N. Bone1,6,7, Olufunmilola Oyebamiji2, Sayali Talware2, Sharmila Selvaraj2, Preethi Krishnan3,6, Farooq Syed1,6,7, Huanmei Wu2, Carmella Evans-Molina 1,3,4,5,6,7,8* Departments of 1Pediatrics, 3Medicine, 4Anatomy, Cell Biology & Physiology, 5Biochemistry & Molecular Biology, the 6Center for Diabetes & Metabolic Diseases, and the 7Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202; 2Department of BioHealth Informatics, Indiana University-Purdue University Indianapolis, Indianapolis, IN, 46202; 8Roudebush VA Medical Center, Indianapolis, IN 46202. *Corresponding Author(s): Carmella Evans-Molina, MD, PhD ([email protected]) Indiana University School of Medicine, 635 Barnhill Drive, MS 2031A, Indianapolis, IN 46202, Telephone: (317) 274-4145, Fax (317) 274-4107 Running Title: Golgi Stress Response in Diabetes Word Count: 4358 Number of Figures: 6 Keywords: Golgi apparatus stress, Islets, β cell, Type 1 diabetes, Type 2 diabetes 1 Diabetes Publish Ahead of Print, published online August 20, 2020 Diabetes Page 2 of 781 ABSTRACT The Golgi apparatus (GA) is an important site of insulin processing and granule maturation, but whether GA organelle dysfunction and GA stress are present in the diabetic β-cell has not been tested. We utilized an informatics-based approach to develop a transcriptional signature of β-cell GA stress using existing RNA sequencing and microarray datasets generated using human islets from donors with diabetes and islets where type 1(T1D) and type 2 diabetes (T2D) had been modeled ex vivo. To narrow our results to GA-specific genes, we applied a filter set of 1,030 genes accepted as GA associated.
    [Show full text]
  • The Role of Phospholipases A2 in Schizophrenia
    Molecular Psychiatry (2006) 11, 547–556 & 2006 Nature Publishing Group All rights reserved 1359-4184/06 $30.00 www.nature.com/mp FEATURE REVIEW The role of phospholipases A2 in schizophrenia MH Law1, RGH Cotton1 and GE Berger1,2 1Genomic Disorders Research Centre, Melbourne, VI, Australia and 2ORYGEN Research Centre, Melbourne, VI, Australia A range of neurotransmitter systems have been implicated in the pathogenesis of schizophrenia based on the antidopaminergic activities of antipsychotic medications, and chemicals that can induce psychotic-like symptoms, such as ketamine or PCP. Such neurotransmitter systems often mediate their cellular response via G-protein-coupled release of arachidonic acid (AA) via the activation of phospholipases A2 (PLA2s). The interaction of three PLA2s are important for the regulation of the release of AA – phospholipase A2 Group 2 A, phospholipase A2 Group 4A and phospholipase A2 Group 6A. Gene variations of these three key enzymes have been associated with schizophrenia with conflicting results. Preclinical data suggest that the activity of these three enzymes are associated with monoaminergic neurotransmission, and may contribute to the differential efficacy of antipsychotic medications, as well as other biological changes thought to underlie schizophrenia, such as altered neurodevelopment and synaptic remodelling. We review the evidence and discuss the potential roles of these three key enzymes for schizophrenia with particular emphasis on published association studies. Molecular Psychiatry (2006) 11, 547–556. doi:10.1038/sj.mp.4001819; published online 4 April 2006 Keywords: review; schizophrenia/genetics; PLA2/genetics; arachidonic acid; common diseases; PLA2/schizophrenia Introduction (PLA2GVIA, PLA2G6A), dopamine, serotonin, G- protein-coupled receptor, eicosanoids and phospho- Neurotransmitters, such as dopamine, serotonin and lipids.
    [Show full text]
  • Genetic and Genomic Analysis of Hyperlipidemia, Obesity and Diabetes Using (C57BL/6J × TALLYHO/Jngj) F2 Mice
    University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Nutrition Publications and Other Works Nutrition 12-19-2010 Genetic and genomic analysis of hyperlipidemia, obesity and diabetes using (C57BL/6J × TALLYHO/JngJ) F2 mice Taryn P. Stewart Marshall University Hyoung Y. Kim University of Tennessee - Knoxville, [email protected] Arnold M. Saxton University of Tennessee - Knoxville, [email protected] Jung H. Kim Marshall University Follow this and additional works at: https://trace.tennessee.edu/utk_nutrpubs Part of the Animal Sciences Commons, and the Nutrition Commons Recommended Citation BMC Genomics 2010, 11:713 doi:10.1186/1471-2164-11-713 This Article is brought to you for free and open access by the Nutrition at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Nutrition Publications and Other Works by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. Stewart et al. BMC Genomics 2010, 11:713 http://www.biomedcentral.com/1471-2164/11/713 RESEARCH ARTICLE Open Access Genetic and genomic analysis of hyperlipidemia, obesity and diabetes using (C57BL/6J × TALLYHO/JngJ) F2 mice Taryn P Stewart1, Hyoung Yon Kim2, Arnold M Saxton3, Jung Han Kim1* Abstract Background: Type 2 diabetes (T2D) is the most common form of diabetes in humans and is closely associated with dyslipidemia and obesity that magnifies the mortality and morbidity related to T2D. The genetic contribution to human T2D and related metabolic disorders is evident, and mostly follows polygenic inheritance. The TALLYHO/ JngJ (TH) mice are a polygenic model for T2D characterized by obesity, hyperinsulinemia, impaired glucose uptake and tolerance, hyperlipidemia, and hyperglycemia.
    [Show full text]
  • A General Binding Mechanism for All Human Sulfatases by the Formylglycine-Generating Enzyme
    A general binding mechanism for all human sulfatases by the formylglycine-generating enzyme Dirk Roeser*, Andrea Preusser-Kunze†, Bernhard Schmidt†, Kathrin Gasow*, Julia G. Wittmann*, Thomas Dierks‡, Kurt von Figura†, and Markus Georg Rudolph*§ *Department of Molecular Structural Biology, University of Go¨ttingen, Justus-von-Liebig-Weg 11, D-37077 Go¨ttingen, Germany; †Department of Biochemistry II, Heinrich-Du¨ker-Weg 12, University of Go¨ttingen, D-37073 Go¨ttingen, Germany; and ‡Department of Biochemistry I, Universita¨tsstrasse 25, University of Bielefeld, D-33615 Bielefeld, Germany Edited by Carolyn R. Bertozzi, University of California, Berkeley, CA, and approved November 8, 2005 (received for review September 1, 2005) The formylglycine (FGly)-generating enzyme (FGE) uses molecular tases, suggesting a general binding mechanism of substrate sulfa- oxygen to oxidize a conserved cysteine residue in all eukaryotic tases by FGE. sulfatases to the catalytically active FGly. Sulfatases degrade and The details of how O2-dependent cysteine oxidation is mediated remodel sulfate esters, and inactivity of FGE results in multiple by FGE are unknown. As a first step toward the elucidation of the sulfatase deficiency, a fatal disease. The previously determined FGE molecular mechanism of FGly formation, we have previously crystal structure revealed two crucial cysteine residues in the active determined crystal structures of FGE in various oxidation states site, one of which was thought to be implicated in substrate (8). FGE adopts a novel fold with surprisingly little regular sec- 2ϩ binding. The other cysteine residue partakes in a novel oxygenase ondary structure and contains two structural Ca ions and two mechanism that does not rely on any cofactors.
    [Show full text]
  • Fine Mapping Studies of Quantitative Trait Loci for Baseline Platelet Count in Mice and Humans
    Fine mapping studies of quantitative trait loci for baseline platelet count in mice and humans A thesis submitted in fulfillment of the requirements for the degree of Doctor of Philosophy Melody C Caramins December 2010 University of New South Wales ORIGINALITY STATEMENT ‘I hereby declare that this submission is my own work and to the best of my knowledge it contains no materials previously published or written by another person, or substantial proportions of material which have been accepted for the award of any other degree or diploma at UNSW or any other educational institution, except where due acknowledgement is made in the thesis. Any contribution made to the research by others, with whom I have worked at UNSW or elsewhere, is explicitly acknowledged in the thesis. I also declare that the intellectual content of this thesis is the product of my own work, except to the extent that assistance from others in the project's design and conception or in style, presentation and linguistic expression is acknowledged.’ Signed …………………………………………….............. Date …………………………………………….............. This thesis is dedicated to my father. Dad, thanks for the genes – and the environment! ACKNOWLEDGEMENTS “Nothing can come out of nothing, any more than a thing can go back to nothing.” - Marcus Aurelius Antoninus A PhD thesis is never the work of one person in isolation from the world at large. I would like to thank the following people, without whom this work would not have existed. Thank you firstly, to all my teachers, of which there have been many. Undoubtedly, the greatest debt is owed to my supervisor, Dr Michael Buckley.
    [Show full text]
  • Genome-Wide DNA Methylation Analysis of KRAS Mutant Cell Lines Ben Yi Tew1,5, Joel K
    www.nature.com/scientificreports OPEN Genome-wide DNA methylation analysis of KRAS mutant cell lines Ben Yi Tew1,5, Joel K. Durand2,5, Kirsten L. Bryant2, Tikvah K. Hayes2, Sen Peng3, Nhan L. Tran4, Gerald C. Gooden1, David N. Buckley1, Channing J. Der2, Albert S. Baldwin2 ✉ & Bodour Salhia1 ✉ Oncogenic RAS mutations are associated with DNA methylation changes that alter gene expression to drive cancer. Recent studies suggest that DNA methylation changes may be stochastic in nature, while other groups propose distinct signaling pathways responsible for aberrant methylation. Better understanding of DNA methylation events associated with oncogenic KRAS expression could enhance therapeutic approaches. Here we analyzed the basal CpG methylation of 11 KRAS-mutant and dependent pancreatic cancer cell lines and observed strikingly similar methylation patterns. KRAS knockdown resulted in unique methylation changes with limited overlap between each cell line. In KRAS-mutant Pa16C pancreatic cancer cells, while KRAS knockdown resulted in over 8,000 diferentially methylated (DM) CpGs, treatment with the ERK1/2-selective inhibitor SCH772984 showed less than 40 DM CpGs, suggesting that ERK is not a broadly active driver of KRAS-associated DNA methylation. KRAS G12V overexpression in an isogenic lung model reveals >50,600 DM CpGs compared to non-transformed controls. In lung and pancreatic cells, gene ontology analyses of DM promoters show an enrichment for genes involved in diferentiation and development. Taken all together, KRAS-mediated DNA methylation are stochastic and independent of canonical downstream efector signaling. These epigenetically altered genes associated with KRAS expression could represent potential therapeutic targets in KRAS-driven cancer. Activating KRAS mutations can be found in nearly 25 percent of all cancers1.
    [Show full text]
  • Análise Integrativa De Perfis Transcricionais De Pacientes Com
    UNIVERSIDADE DE SÃO PAULO FACULDADE DE MEDICINA DE RIBEIRÃO PRETO PROGRAMA DE PÓS-GRADUAÇÃO EM GENÉTICA ADRIANE FEIJÓ EVANGELISTA Análise integrativa de perfis transcricionais de pacientes com diabetes mellitus tipo 1, tipo 2 e gestacional, comparando-os com manifestações demográficas, clínicas, laboratoriais, fisiopatológicas e terapêuticas Ribeirão Preto – 2012 ADRIANE FEIJÓ EVANGELISTA Análise integrativa de perfis transcricionais de pacientes com diabetes mellitus tipo 1, tipo 2 e gestacional, comparando-os com manifestações demográficas, clínicas, laboratoriais, fisiopatológicas e terapêuticas Tese apresentada à Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo para obtenção do título de Doutor em Ciências. Área de Concentração: Genética Orientador: Prof. Dr. Eduardo Antonio Donadi Co-orientador: Prof. Dr. Geraldo A. S. Passos Ribeirão Preto – 2012 AUTORIZO A REPRODUÇÃO E DIVULGAÇÃO TOTAL OU PARCIAL DESTE TRABALHO, POR QUALQUER MEIO CONVENCIONAL OU ELETRÔNICO, PARA FINS DE ESTUDO E PESQUISA, DESDE QUE CITADA A FONTE. FICHA CATALOGRÁFICA Evangelista, Adriane Feijó Análise integrativa de perfis transcricionais de pacientes com diabetes mellitus tipo 1, tipo 2 e gestacional, comparando-os com manifestações demográficas, clínicas, laboratoriais, fisiopatológicas e terapêuticas. Ribeirão Preto, 2012 192p. Tese de Doutorado apresentada à Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo. Área de Concentração: Genética. Orientador: Donadi, Eduardo Antonio Co-orientador: Passos, Geraldo A. 1. Expressão gênica – microarrays 2. Análise bioinformática por module maps 3. Diabetes mellitus tipo 1 4. Diabetes mellitus tipo 2 5. Diabetes mellitus gestacional FOLHA DE APROVAÇÃO ADRIANE FEIJÓ EVANGELISTA Análise integrativa de perfis transcricionais de pacientes com diabetes mellitus tipo 1, tipo 2 e gestacional, comparando-os com manifestações demográficas, clínicas, laboratoriais, fisiopatológicas e terapêuticas.
    [Show full text]
  • Supplementary Table S2
    1-high in cerebrotropic Gene P-value patients Definition BCHE 2.00E-04 1 Butyrylcholinesterase PLCB2 2.00E-04 -1 Phospholipase C, beta 2 SF3B1 2.00E-04 -1 Splicing factor 3b, subunit 1 BCHE 0.00022 1 Butyrylcholinesterase ZNF721 0.00028 -1 Zinc finger protein 721 GNAI1 0.00044 1 Guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 1 GNAI1 0.00049 1 Guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 1 PDE1B 0.00069 -1 Phosphodiesterase 1B, calmodulin-dependent MCOLN2 0.00085 -1 Mucolipin 2 PGCP 0.00116 1 Plasma glutamate carboxypeptidase TMX4 0.00116 1 Thioredoxin-related transmembrane protein 4 C10orf11 0.00142 1 Chromosome 10 open reading frame 11 TRIM14 0.00156 -1 Tripartite motif-containing 14 APOBEC3D 0.00173 -1 Apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3D ANXA6 0.00185 -1 Annexin A6 NOS3 0.00209 -1 Nitric oxide synthase 3 SELI 0.00209 -1 Selenoprotein I NYNRIN 0.0023 -1 NYN domain and retroviral integrase containing ANKFY1 0.00253 -1 Ankyrin repeat and FYVE domain containing 1 APOBEC3F 0.00278 -1 Apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3F EBI2 0.00278 -1 Epstein-Barr virus induced gene 2 ETHE1 0.00278 1 Ethylmalonic encephalopathy 1 PDE7A 0.00278 -1 Phosphodiesterase 7A HLA-DOA 0.00305 -1 Major histocompatibility complex, class II, DO alpha SOX13 0.00305 1 SRY (sex determining region Y)-box 13 ABHD2 3.34E-03 1 Abhydrolase domain containing 2 MOCS2 0.00334 1 Molybdenum cofactor synthesis 2 TTLL6 0.00365 -1 Tubulin tyrosine ligase-like family, member 6 SHANK3 0.00394 -1 SH3 and multiple ankyrin repeat domains 3 ADCY4 0.004 -1 Adenylate cyclase 4 CD3D 0.004 -1 CD3d molecule, delta (CD3-TCR complex) (CD3D), transcript variant 1, mRNA.
    [Show full text]