ABCMdb reloaded: updates on mutations in ATP binding cassette proteins

Abstract ABC (ATP-Binding Cassette) proteins with altered function are responsible for numerous human diseases. To aid the selection of positions and amino acids for ABC structure/function studies we have generated a database, ABCMdb (Gyimesi et al., ABCMdb: a database for the comparative analysis of protein mutations in ABC transporters, and a potential framework for a general application. Hum Mutat 2012; 33:1547–1556.), with interactive tools. The database has been populated with mentions of mutations extracted from full text papers, alignments and structural models. In the new version of the database we aimed to collect the effect of mutations from databases including ClinVar. Because of the low number of available data, even in the case of the widely studied disease-causing ABC proteins, we also included the possible effects of mutations based on SNAP2 and PROVEAN predictions. To aid the interpretation of variations in non-coding regions, the database was supplemented with related DNA level information. Our results emphasize the importance of in silico predictions because of the sparse information available on variants and suggest that mutations at analogous positions in homologous ABC proteins have a strong predictive power for the effects of mutations. Our improved ABCMdb advances the design of both experimental studies and meta-analyses in order to understand drug interactions of ABC proteins and the effects of mutations on functional expression. Database URL: http://abcm2.hegelab.org

[1]  P. Borst,et al.  Mammalian ABC transporters in health and disease. , 2002, Annual review of biochemistry.

[2]  Yongwook Choi,et al.  PROVEAN web server: a tool to predict the functional effect of amino acid substitutions and indels , 2015, Bioinform..

[3]  S. Terry Disease advocacy organizations catalyze translational research , 2013, Front. Genet..

[4]  J. Stindt,et al.  The bile salt export pump (BSEP) in health and disease. , 2012, Clinics and research in hepatology and gastroenterology.

[5]  J. Bryan,et al.  ABCC8 and ABCC9: ABC transporters that regulate K+ channels , 2007, Pflügers Archiv - European Journal of Physiology.

[6]  S. Kosak,et al.  Differential contribution of cis-regulatory elements to higher order chromatin structure and expression of the CFTR locus , 2015, Nucleic acids research.

[7]  S. Cole,et al.  Functional characterization of non-synonymous single nucleotide polymorphisms in the gene encoding human multidrug resistance protein 1 (MRP1/ABCC1) , 2005, Pharmacogenetics and genomics.

[8]  Deanna M. Church,et al.  ClinVar: public archive of relationships among sequence variation and human phenotype , 2013, Nucleic Acids Res..

[9]  G. Gyimesi,et al.  ABCMdb: A database for the comparative analysis of protein mutations in ABC transporters, and a potential framework for a general application , 2012, Human mutation.

[10]  J. Miller,et al.  Predicting the Functional Effect of Amino Acid Substitutions and Indels , 2012, PloS one.

[11]  W. Hauswirth,et al.  A comprehensive review of retinal gene therapy. , 2013, Molecular therapy : the journal of the American Society of Gene Therapy.

[12]  P. Underhill,et al.  Molecular dissection of the Y chromosome haplogroup E‐M78 (E3b1a): a posteriori evaluation of a microsatellite‐network‐based approach through six new biallelic markers , 2006, Human mutation.

[13]  T. Arányi,et al.  ABCC6 as a target in pseudoxanthoma elasticum. , 2011, Current drug targets.

[14]  K. Kleesiek,et al.  Mutational analysis of the ABCC6 gene and the proximal ABCC6 gene promoter in German patients with pseudoxanthoma elasticum (PXE) , 2006, Human mutation.

[15]  F. Lammert,et al.  The genetics of complex cholestatic disorders. , 2013, Gastroenterology.

[16]  Jing Li,et al.  Association of variant ABCG2 and the pharmacokinetics of epidermal growth factor receptor tyrosine kinase inhibitors in cancer patients , 2007, Cancer biology & therapy.

[17]  M. Corey,et al.  Do common in silico tools predict the clinical consequences of amino‐acid substitutions in the CFTR gene? , 2010, Clinical genetics.

[18]  P. Thomas,et al.  Alteration of the Cystic Fibrosis Transmembrane Conductance Regulator Folding Pathway , 1996, The Journal of Biological Chemistry.

[19]  K. Faber,et al.  Farnesoid X receptor and bile salts are involved in transcriptional regulation of the gene encoding the human bile salt export pump , 2002, Hepatology.

[20]  Elizabeth M. Smigielski,et al.  dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..

[21]  Bartek Wilczynski,et al.  Biopython: freely available Python tools for computational molecular biology and bioinformatics , 2009, Bioinform..

[22]  Richard J. Thompson,et al.  Missense mutations and single nucleotide polymorphisms in ABCB11 impair bile salt export pump processing and function or disrupt pre‐messenger RNA splicing , 2009, Hepatology.

[23]  J. Boyer,et al.  Nuclear factor erythroid 2–related factor 2 is a positive regulator of human bile salt export pump expression , 2009, Hepatology.

[24]  Mauno Vihinen,et al.  Performance of protein stability predictors , 2010, Human mutation.

[25]  B. Sarkadi,et al.  Jump into a New Fold—A Homology Based Model for the ABCG2/BCRP Multidrug Transporter , 2016, PloS one.

[26]  M. Vihinen,et al.  Variation Interpretation Predictors: Principles, Types, Performance, and Choice , 2016, Human mutation.

[27]  J. Uitto,et al.  Transcriptional regulation and characterization of the promoter region of the human ABCC6 gene. , 2006, The Journal of investigative dermatology.

[28]  P. Závodszky,et al.  Clustering of disease-causing mutations on the domain-domain interfaces of ABCC6. , 2009, Biochemical and biophysical research communications.

[29]  J. Uitto,et al.  Analysis of Pseudoxanthoma Elasticum-Causing Missense Mutants of ABCC6 in vivo; Pharmacological Correction of the Mislocalized Proteins , 2013, The Journal of investigative dermatology.

[30]  Liang Feng,et al.  Structure of a Eukaryotic CLC Transporter Defines an Intermediate State in the Transport Cycle , 2010, Science.

[31]  Andrei Aleksandrov,et al.  Domain interdependence in the biosynthetic assembly of CFTR. , 2007, Journal of molecular biology.

[32]  A. M. George ABC Transporters - 40 Years on , 2016, Springer International Publishing.

[33]  M. Phillips Molecular Mechanisms of Cellular Cholesterol Efflux* , 2014, The Journal of Biological Chemistry.

[34]  Garry R. Cutting,et al.  From CFTR biology toward combinatorial pharmacotherapy: expanded classification of cystic fibrosis mutations , 2016, Molecular biology of the cell.

[35]  K. Matsuda,et al.  Association Study of a Functional Variant on ABCG2 Gene with Sunitinib-Induced Severe Adverse Drug Reaction , 2016, PloS one.

[36]  Balázs Sarkadi,et al.  The role of ABC transporters in drug absorption, distribution, metabolism, excretion and toxicity (ADME-Tox). , 2008, Drug discovery today.

[37]  Morris Swertz,et al.  Cafe Variome: General‐Purpose Software for Making Genotype–Phenotype Data Discoverable in Restricted or Open Access Contexts , 2015, Human mutation.

[38]  M. Makishima,et al.  Human Bile Salt Export Pump Promoter Is Transactivated by the Farnesoid X Receptor/Bile Acid Receptor* , 2001, The Journal of Biological Chemistry.

[39]  G. Schreiber,et al.  Assessing computational methods for predicting protein stability upon mutation: good on average but not in the details. , 2009, Protein engineering, design & selection : PEDS.

[40]  A. Harris,et al.  Chromatin remodeling mediated by the FOXA1/A2 transcription factors activates CFTR expression in intestinal epithelial cells , 2014, Epigenetics.

[41]  B. Rost,et al.  Better prediction of functional effects for sequence variants , 2015, BMC Genomics.

[42]  P. Bork,et al.  A method and server for predicting damaging missense mutations , 2010, Nature Methods.

[43]  C. Castellani,et al.  CFTR2: How will it help care? , 2013, Paediatric respiratory reviews.

[44]  K. Noguchi,et al.  Pharmacological interaction with sunitinib is abolished by a germ‐line mutation (1291T>C) of BCRP/ABCG2 gene , 2010, Cancer science.

[45]  W. V. D. Van de Ven,et al.  The human pseudoxanthoma elasticum gene ABCC6 is transcriptionally regulated by PLAG family transcription factors , 2008, Human Genetics.

[46]  Kai Du,et al.  Cooperative assembly and misfolding of CFTR domains in vivo. , 2009, Molecular biology of the cell.

[47]  G. Szakács,et al.  Human multidrug resistance ABCB and ABCG transporters: participation in a chemoimmunity defense system. , 2006, Physiological reviews.

[48]  Daniel Lai,et al.  Assessment of the predictive accuracy of five in silico prediction tools, alone or in combination, and two metaservers to classify long QT syndrome gene mutations , 2015, BMC Medical Genetics.

[49]  Jeroen F. J. Laros,et al.  LOVD v.2.0: the next generation in gene variant databases , 2011, Human mutation.

[50]  Guorong Xu,et al.  Faculty Opinions recommendation of Liver receptor homolog 1 transcriptionally regulates human bile salt export pump expression. , 2008 .

[51]  A. Harris,et al.  Transcriptional networks driving enhancer function in the CFTR gene. , 2012, The Biochemical journal.

[52]  L. Pulaski,et al.  Liver-specific enhancer in ABCC6 promoter-Functional evidence from natural polymorphisms. , 2009, Biochemical and biophysical research communications.

[53]  J. Riordan,et al.  CFTR function and prospects for therapy. , 2008, Annual review of biochemistry.

[54]  Jonathan C. Cohen,et al.  Crystal structure of the human sterol transporter ABCG5/ABCG8 , 2016, Nature.

[55]  Yang Yang,et al.  PON-Sol: prediction of effects of amino acid substitutions on protein solubility , 2016, Bioinform..

[56]  R. Dalgleish The Hemoglobinopathies : A Model Example for LSDBs , 2016 .

[57]  S. Cha,et al.  TAP1, TAP2, and HLA-DR2 alleles are predictors of cervical cancer risk. , 2003, Gynecologic oncology.

[58]  R. Tampé,et al.  The transporter associated with antigen processing: a key player in adaptive immunity , 2015, Biological chemistry.

[59]  P. Thomas,et al.  Coding single-nucleotide polymorphisms associated with complex vs. Mendelian disease: evolutionary evidence for differences in molecular effects. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[60]  K. Locher Structure and mechanism of ATP-binding cassette transporters , 2009, Philosophical Transactions of the Royal Society B: Biological Sciences.