Supplementary Table 5. the 917 Candidate Marker Genes for the Diagnostic Model for Early HCC in the Training Set
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Reconstruction of the Global Neural Crest Gene Regulatory Network in Vivo
Reconstruction of the global neural crest gene regulatory network in vivo Ruth M Williams1, Ivan Candido-Ferreira1, Emmanouela Repapi2, Daria Gavriouchkina1,4, Upeka Senanayake1, Jelena Telenius2,3, Stephen Taylor2, Jim Hughes2,3, and Tatjana Sauka-Spengler1,∗ Supplemental Material ∗Lead and corresponding author: Tatjana Sauka-Spengler ([email protected]) 1University of Oxford, MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, Oxford, OX3 9DS, UK 2University of Oxford, MRC Centre for Computational Biology, MRC Weatherall Institute of Molecular Medicine, Oxford, OX3 9DS, UK 3University of Oxford, MRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, Oxford, OX3 9DS, UK 4Present Address: Okinawa Institute of Science and Technology, Molecular Genetics Unit, Onna, 904-0495, Japan A 25 25 25 25 25 20 20 20 20 20 15 15 15 15 15 10 10 10 10 10 log2(R1_5-6ss) log2(R1_5-6ss) log2(R1_8-10ss) log2(R1_8-10ss) log2(R1_non-NC) 5 5 5 5 5 0 r=0.92 0 r=0.99 0 r=0.96 0 r=0.99 0 r=0.96 0 5 10 15 20 25 0 5 10 15 20 25 0 5 10 15 20 25 0 5 10 15 20 25 0 5 10 15 20 25 log2(R2_non-NC) log2(R2_5-6ss) log2(R3_5-6ss) log2(R2_8-10ss) log2(R3_8-10ss) 25 25 25 25 25 20 20 20 20 20 15 15 15 15 15 10 10 10 10 10 log2(R1_5-6ss) log2(R2_5-6ss) log2(R1_8-10ss) log2(R2_8-10ss) log2(R1_non-NC) 5 5 5 5 5 0 r=0.94 0 r=0.96 0 r=0.95 0 r=0.96 0 r=0.95 0 5 10 15 20 25 0 5 10 15 20 25 0 5 10 15 20 25 0 5 10 15 20 25 0 5 10 15 20 25 log2(R3_non-NC) log2(R4_5-6ss) log2(R3_5-6ss) log2(R4_8-10ss) log2(R3_8-10ss) -
Gene PMID WBS Locus ABR 26603386 AASDH 26603386
Supplementary material J Med Genet Gene PMID WBS Locus ABR 26603386 AASDH 26603386 ABCA1 21304579 ABCA13 26603386 ABCA3 25501393 ABCA7 25501393 ABCC1 25501393 ABCC3 25501393 ABCG1 25501393 ABHD10 21304579 ABHD11 25501393 yes ABHD2 25501393 ABHD5 21304579 ABLIM1 21304579;26603386 ACOT12 25501393 ACSF2,CHAD 26603386 ACSL4 21304579 ACSM3 26603386 ACTA2 25501393 ACTN1 26603386 ACTN3 26603386;25501393;25501393 ACTN4 21304579 ACTR1B 21304579 ACVR2A 21304579 ACY3 19897463 ACYP1 21304579 ADA 25501393 ADAM12 21304579 ADAM19 25501393 ADAM32 26603386 ADAMTS1 25501393 ADAMTS10 25501393 ADAMTS12 26603386 ADAMTS17 26603386 ADAMTS6 21304579 ADAMTS7 25501393 ADAMTSL1 21304579 ADAMTSL4 25501393 ADAMTSL5 25501393 ADCY3 25501393 ADK 21304579 ADRBK2 25501393 AEBP1 25501393 AES 25501393 AFAP1,LOC84740 26603386 AFAP1L2 26603386 AFG3L1 21304579 AGAP1 26603386 AGAP9 21304579 Codina-Sola M, et al. J Med Genet 2019; 56:801–808. doi: 10.1136/jmedgenet-2019-106080 Supplementary material J Med Genet AGBL5 21304579 AGPAT3 19897463;25501393 AGRN 25501393 AGXT2L2 25501393 AHCY 25501393 AHDC1 26603386 AHNAK 26603386 AHRR 26603386 AIDA 25501393 AIFM2 21304579 AIG1 21304579 AIP 21304579 AK5 21304579 AKAP1 25501393 AKAP6 21304579 AKNA 21304579 AKR1E2 26603386 AKR7A2 21304579 AKR7A3 26603386 AKR7L 26603386 AKT3 21304579 ALDH18A1 25501393;25501393 ALDH1A3 21304579 ALDH1B1 21304579 ALDH6A1 21304579 ALDOC 21304579 ALG10B 26603386 ALG13 21304579 ALKBH7 25501393 ALPK2 21304579 AMPH 21304579 ANG 21304579 ANGPTL2,RALGPS1 26603386 ANGPTL6 26603386 ANK2 21304579 ANKMY1 26603386 ANKMY2 -
Transcriptional and Post-Transcriptional Regulation of ATP-Binding Cassette Transporter Expression
Transcriptional and Post-transcriptional Regulation of ATP-binding Cassette Transporter Expression by Aparna Chhibber DISSERTATION Submitted in partial satisfaction of the requirements for the degree of DOCTOR OF PHILOSOPHY in Pharmaceutical Sciences and Pbarmacogenomies in the Copyright 2014 by Aparna Chhibber ii Acknowledgements First and foremost, I would like to thank my advisor, Dr. Deanna Kroetz. More than just a research advisor, Deanna has clearly made it a priority to guide her students to become better scientists, and I am grateful for the countless hours she has spent editing papers, developing presentations, discussing research, and so much more. I would not have made it this far without her support and guidance. My thesis committee has provided valuable advice through the years. Dr. Nadav Ahituv in particular has been a source of support from my first year in the graduate program as my academic advisor, qualifying exam committee chair, and finally thesis committee member. Dr. Kathy Giacomini graciously stepped in as a member of my thesis committee in my 3rd year, and Dr. Steven Brenner provided valuable input as thesis committee member in my 2nd year. My labmates over the past five years have been incredible colleagues and friends. Dr. Svetlana Markova first welcomed me into the lab and taught me numerous laboratory techniques, and has always been willing to act as a sounding board. Michael Martin has been my partner-in-crime in the lab from the beginning, and has made my days in lab fly by. Dr. Yingmei Lui has made the lab run smoothly, and has always been willing to jump in to help me at a moment’s notice. -
Modeling Enhancer-Promoter Interactions with Attention-Based Neural Networks
bioRxiv preprint doi: https://doi.org/10.1101/219667; this version posted November 14, 2017. 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-NC-ND 4.0 International license. Article Modeling Enhancer-Promoter Interactions with Attention-Based Neural Networks Weiguang Mao 1,2, Dennis Kostka 1,2,3 and Maria Chikina 1,2* 1 Department of Computational and Systems Biology, School of Medicine, University of Pittsburgh 2 Joint Carnegie Mellon - University of Pittsburgh Ph.D. Program in Computational Biology 3 Department of Developmental Biology, School of Medicine, University of Pittsburgh * Correspondence: [email protected] Academic Editor: name Version November 9, 2017 submitted to Cells 1 Abstract: Background: Gene regulatory sequences play critical roles in ensuring tightly controlled 2 RNA expression patterns that are essential in a large variety of biological processes. Specifically, 3 enhancer sequences drive expression of their target genes, and the availability of genome-wide 4 maps of enhancer-promoter interactions has opened up the possibility to use machine learning 5 approaches to extract and interpret features that define these interactions in different biological 6 contexts. Methods: Inspired by machine translation models we develop an attention-based neural 7 network model, EPIANN, to predict enhancer-promoter interactions based on DNA sequences. Codes 8 and data are available at https://github.com/wgmao/EPIANN. Results: Our approach accurately 9 predicts enhancer-promoter interactions across six cell lines. In addition, our method generates 10 pairwise attention scores at the sequence level, which specify how short regions in the enhancer and 11 promoter pair-up to drive the interaction prediction. -
Upregulation of the Transcription Factor TFAP2D Is Associated With
Fraune et al. Molecular Medicine (2020) 26:24 Molecular Medicine https://doi.org/10.1186/s10020-020-00148-4 RESEARCH ARTICLE Open Access Upregulation of the transcription factor TFAP2D is associated with aggressive tumor phenotype in prostate cancer lacking the TMPRSS2:ERG fusion Christoph Fraune1†, Luisa Harms1†, Franziska Büscheck1, Doris Höflmayer1, Maria Christina Tsourlakis1, Till S. Clauditz1, Ronald Simon1* , Katharina Möller1, Andreas M. Luebke1, Christina Möller-Koop1, Stefan Steurer1, Claudia Hube-Magg1, Guido Sauter1, Sören Weidemann1, Patrick Lebok1, David Dum1, Simon Kind1, Sarah Minner1, Jakob R. Izbicki2, Thorsten Schlomm3, Hartwig Huland4, Hans Heinzer4, Eike Burandt1, Alexander Haese4, Markus Graefen4 and Cornelia Schroeder2 Abstract Background: TFAP2D is a transcription factor important for modulating gene expression in embryogenesis. Its expression and prognostic role in prostate cancer has not been evaluated. Methods: Therefore, a tissue microarray containing 17,747 prostate cancer specimens with associated pathological, clinical, and molecular data was analyzed by immunohistochemistry to assess the role of TFAP2D. Results: TFAP2D expression was typically increased in prostate cancer as compared to adjacent non-neoplastic glands. TFAP2D staining was considered negative in 24.3% and positive in 75.7% of 13,545 interpretable cancers. TFAP2D staining was significantly linked to advanced tumor stage, high classical and quantitative Gleason grade, lymph node metastasis, and a positive surgical margin (p ≤ 0.0045). TFAP2D positivity was more common in ERG fusion positive (88.7%) than in ERG negative cancers (66.8%; p < 0.0001). Subset analyses in 3776 cancers with and 4722 cancers without TMPRSS2:ERG fusion revealed that associations with tumor phenotype and patient outcome were largely driven by the subset of ERG negative tumors. -
Co-Regulation of Hormone Receptors, Neuropeptides, and Steroidogenic Enzymes 2 Across the Vertebrate Social Behavior Network 3 4 Brent M
bioRxiv preprint doi: https://doi.org/10.1101/435024; this version posted October 4, 2018. 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-NC-ND 4.0 International license. 1 Co-regulation of hormone receptors, neuropeptides, and steroidogenic enzymes 2 across the vertebrate social behavior network 3 4 Brent M. Horton1, T. Brandt Ryder2, Ignacio T. Moore3, Christopher N. 5 Balakrishnan4,* 6 1Millersville University, Department of Biology 7 2Smithsonian Conservation Biology Institute, Migratory Bird Center 8 3Virginia Tech, Department of Biological Sciences 9 4East Carolina University, Department of Biology 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 1 bioRxiv preprint doi: https://doi.org/10.1101/435024; this version posted October 4, 2018. 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-NC-ND 4.0 International license. 1 Running Title: Gene expression in the social behavior network 2 Keywords: dominance, systems biology, songbird, territoriality, genome 3 Corresponding Author: 4 Christopher Balakrishnan 5 East Carolina University 6 Department of Biology 7 Howell Science Complex 8 Greenville, NC, USA 27858 9 [email protected] 10 2 bioRxiv preprint doi: https://doi.org/10.1101/435024; this version posted October 4, 2018. 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. -
Regulation of the Kras Promoter in Pancreatic Cancer by Proteins and Small Molecules
University of Mississippi eGrove Electronic Theses and Dissertations Graduate School 1-1-2017 Regulation of the kRAS Promoter in Pancreatic Cancer by Proteins and Small Molecules Harshul Batra University of Mississippi Follow this and additional works at: https://egrove.olemiss.edu/etd Part of the Molecular Biology Commons Recommended Citation Batra, Harshul, "Regulation of the kRAS Promoter in Pancreatic Cancer by Proteins and Small Molecules" (2017). Electronic Theses and Dissertations. 1481. https://egrove.olemiss.edu/etd/1481 This Dissertation is brought to you for free and open access by the Graduate School at eGrove. It has been accepted for inclusion in Electronic Theses and Dissertations by an authorized administrator of eGrove. For more information, please contact [email protected]. REGULATION OF THE kRAS PROMOTER IN PANCREATIC CANCER BY PROTEINS AND SMALL MOLECULES A Dissertation presented in fulfillment of requirements for the degree of Doctorate of Philosophy in the Department of BioMolecular Sciences Division of Pharmacology The University of Mississippi by HARSHUL BATRA August 2017 Copyright © 2017 by Harshul Batra All rights reserved ABSTRACT DNA-binding proteins play a pivotal role in cell biology. The major class of DNA-binding proteins are transcription factors (TFs). TFs are central to almost every fundamental cellular process such as cell development, differentiation, cell growth, and gene expression. They account for 10% of the genes in eukaryotes. In mammals, more than 700 TFs are identified to be DNA- binding TFs. They bind to the TF binding sites (TFBSs) in the genome and regulate the expression of their target genes. kRAS is a proto-oncogene with intrinsic GTPase activity, that contributes to cell proliferation, division, and apoptosis. -
Characterizing Thyroid Hormone Mediated Action on Gene
Characterizing thyroid hormone mediated action on gene expression in mice: mechanistic insight into thyroid hormone response elements, thyroid hormone receptor-binding sites, and microRNAs by Martin A. Paquette A thesis submitted to the Faculty of Graduate and Postdoctoral Affairs in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Biology Carleton University Ottawa, Ontario ©2013 Martin A. Paquette ABSTRACT Thyroid hormone (TH) exerts its effects by binding to the TH receptor (TR), which binds to TH response elements (TREs) to regulate target gene expression. Disruption of TH action can have detrimental health effects. The precise molecular mechanisms involved in TH mediated gene expression remain unclear. The overall objectives of this thesis were to: i) characterize global gene and microRNA (miRNA) expression in early response to TH perturbation in mouse liver; ii) identify TREs and TR-binding sites found throughout the mouse genome; and iii) compare TRE half-site organizations and their ability to drive gene expression. Transcriptional profiling of mRNA liver samples from TH disrupted mice enabled the identification of genes that were under direct TH-regulation. TREs in the promoter region of Tor1a, Hectd3, Slc25a45 and 2310003H01Rik were validated in vitro, adding four genes to the battery of only 13 known TRE- containing mouse genes. Hepatic miRNAs were also found to be significantly altered following perturbations in TH levels. In vitro analyses confirmed TH regulation of miR-206. Moreover, Mup1 and Gpd2 were confirmed to be targeted by miR-206 in response to TH, demonstrating that miRNAs can act as master regulators of the TH response pathway. -
A SILAC-Based DNA Protein Interaction Screen That Identifies Candidate Binding Proteins to Functional DNA Elements
Downloaded from genome.cshlp.org on September 29, 2021 - Published by Cold Spring Harbor Laboratory Press Methods A SILAC-based DNA protein interaction screen that identifies candidate binding proteins to functional DNA elements Gerhard Mittler,1,2,4 Falk Butter,3 and Matthias Mann3,5 1Center for Experimental Bioinformatics, University of Southern Denmark, DK-5230 Odense M, Denmark; 2BIOSS—Center of Biological Signalling Studies, Albert-Ludwigs-University Freiburg, D-79104 Freiburg, Germany; 3Department of Proteomics and Signal Transduction, Max-Planck-Institute for Biochemistry, D-82152 Martinsried, Germany Determining the underlying logic that governs the networks of gene expression in higher eukaryotes is an important task in the post-genome era. Sequence-specific transcription factors (TFs) that can read the genetic regulatory information and proteins that interpret the information provided by CpG methylation are crucial components of the system that controls the transcription of protein-coding genes by RNA polymerase II. We have previously described Stable Isotope Labeling by Amino acids in Cell culture (SILAC) for the quantitative comparison of proteomes and the determination of protein– protein interactions. Here, we report a generic and scalable strategy to uncover such DNA protein interactions by SILAC that uses a fast and simple one-step affinity capture of TFs from crude nuclear extracts. Employing mutated or non- methylated control oligonucleotides, specific TFs binding to their wild-type or methyl-CpG bait are distinguished from the vast excess of copurifying background proteins by their peptide isotope ratios that are determined by mass spec- trometry. Our proof of principle screen identifies several proteins that have not been previously reported to be present on the fully methylated CpG island upstream of the human metastasis associated 1 family, member 2 gene promoter. -
Supplemental Data FOXP2 Targets Show Evidence of Positive
The American Journal of Human Genetics, Volume 92 Supplemental Data FOXP2 Targets Show Evidence of Positive Selection in European Populations Qasim Ayub, Bryndis Yngvadottir, Yuan Chen, Yali Xue, Min Hu, Sonja C. Vernes, Simon E. Fisher, and Chris Tyler-Smith Mouse Brain Human Brain 198 5 186 0 5 72 198 Human Neuronal Cell Figure S1. Overlap of FOXP2 Targets FOXP2 targets were identified in three separate chromatin immunoprecipitation genomic screens. A Generate Euclidean Distances matched for; Target Gene List (n = 208) Gene size 1. ENSG00000071242 GC content 2. ENSG00000168405 Recombination rate 3. ENSG00000204681 . 208. ENSG00000174469 Generate 1,000 nearest Euclidean neighbors for each target gene Target Gene #1 Neighbors 1. 2. Target Gene #2 Neighbors 3. 1. 2. Target Gene #3 Neighbors 3. 1. 1000. 2. 3. Target Gene #208 Neighbors . 1. 1000. 2. 3. 1000. 1000. For each target pick 1/1,000 matched neighbor randomly to generate a control list. Generate 1,000 such lists Matched Control List #1 1. Matched with target gene 1 Matched Control List #2 2. Matched with target gene 2 1. Matched with target gene 1 3. Matched with target gene 3 2. MatchedMatched with target Control gene List 2 #3 . 1. Matched with target gene 1 3. Matched with target geneMatched 3 Control List #1000 . 2. Matched with target gene 2 . 1. Matched with target gene 1 . 3. Matched with target gene 3 . 2. Matched with target gene 2 208. Matched with target gene. 3. Matched with target gene 3 . 208. Matched with target gene. 208. Matched with target gen . 208. -
Downloaded a Meta
bioRxiv preprint doi: https://doi.org/10.1101/2020.07.18.210328; this version posted April 12, 2021. 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-NC-ND 4.0 International license. Dynamic regulatory module networks for inference of cell type-specific transcriptional networks Alireza Fotuhi Siahpirani1,2,+, Sara Knaack1+, Deborah Chasman1,8,+, Morten Seirup3,4, Rupa Sridharan1,5, Ron Stewart3, James Thomson3,5,6, and Sushmita Roy1,2,7* 1Wisconsin Institute for Discovery, University of Wisconsin-Madison 2Department of Computer Sciences, University of Wisconsin-Madison 3Morgridge Institute for Research 4Molecular and Environmental Toxicology Program, University of Wisconsin-Madison 5Department of Cell and Regenerative Biology, University of Wisconsin-Madison 6Department of Molecular, Cellular, & Developmental Biology, University of California Santa Barbara 7Department of Biostatistics and Medical Informatics, University of Wisconsin-Madison 8Present address: Division of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Wisconsin-Madison +These authors contributed equally. *To whom correspondence should be addressed. 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.07.18.210328; this version posted April 12, 2021. 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-NC-ND 4.0 International license. Abstract Multi-omic datasets with parallel transcriptomic and epigenomic measurements across time or cell types are becoming increasingly common. -
Antibodies Products
Chapter 2 : Gentaur Products List • WDSUB1 contains 1 SAM sterile alpha motif domain 1 U Defects in DLG3 are the cause of mental retardation X • Sodium hydrogen exchangers NHEs such as SLC9A8 are box domain and 7 WD repeats The function of WDSUB1 linked type 90 MRX90 integral transmembrane proteins that exchange extracellular remains unknown • SLC25A20 is one of several closely related mitochondrial Na for intracellular H NHEs have multiple functions including • RNF217 is an E3 ubiquitin protein ligase which accepts membrane carrier proteins that shuttle substrates between intracellular pH ho ubiquitin from E2 ubiquitin conjugating enzymes in the form cytosol and the intramitochondrial matrix space It mediates • SLCO1C1 is a member of the organic anion transporter of a thioester and then directly transfers the ubiquitin to the transport of acylcarn family SLCO1C1 is a transmembrane receptor that mediates targeted substrates • The sodium iodide symporter NIS or SLC5A5 is a key the sodium independent uptake of thyroid hormones in brain • TRIM60 contains a RING finger domain a motif present in a plasma membrane protein that mediates active I uptake in tissues This protein has part variety of functionally distinct proteins and known to be thyroid lactating breast and other tissues with an • SLC35A5 belongs to the nucleotide sugar transporter involved in protein protein and protein DNA interactions The electrogenic stoichiometry of 2 Na family SLC35A subfamily It is a multi pass membrane protein encoded by thi • SLC2A9 is a member of the SLC2A