A. Maxwell Burroughs

ORCID: 0000-0002-2229-8771
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About
Contact & Profiles
Research Areas
  • RNA and protein synthesis mechanisms
  • RNA modifications and cancer
  • RNA Research and Splicing
  • Bacteriophages and microbial interactions
  • Bacterial Genetics and Biotechnology
  • Genomics and Phylogenetic Studies
  • MicroRNA in disease regulation
  • CRISPR and Genetic Engineering
  • Genomics and Chromatin Dynamics
  • Vibrio bacteria research studies
  • Ubiquitin and proteasome pathways
  • Biochemical and Molecular Research
  • Peptidase Inhibition and Analysis
  • Plant Virus Research Studies
  • Chromosomal and Genetic Variations
  • interferon and immune responses
  • Cancer-related molecular mechanisms research
  • Enzyme Structure and Function
  • RNA Interference and Gene Delivery
  • Evolution and Genetic Dynamics
  • T-cell and B-cell Immunology
  • Glycosylation and Glycoproteins Research
  • Advanced biosensing and bioanalysis techniques
  • Aquaculture disease management and microbiota
  • Immune Cell Function and Interaction

National Center for Biotechnology Information
2016-2025

National Institutes of Health
2016-2025

United States National Library of Medicine
2007-2023

RIKEN Center for Integrative Medical Sciences
2009-2021

NTL Institute for Applied Behavioral Science
2017

RIKEN
2011

Boston University
2006-2008

Alistair R. R. Forrest Hideya Kawaji Michael Rehli J. Kenneth Baillie Michiel de Hoon and 95 more Vanja Haberle Timo Lassmann Ivan V. Kulakovskiy Marina Lizio Masayoshi Itoh Robin Andersson Chris Mungall Terrence F. Meehan Sebastian Schmeier Nicolas Bertin Mette Jørgensen Emmanuel Dimont Peter Arner Christian Schmidl Ulf Schaefer Yulia A. Medvedeva Charles Plessy Morana Vitezic Jessica Severin Colin A. Semple Yuri Ishizu Robert S. Young Margherita Francescatto Intikhab Álam Davide Albanese Gabriel M. Altschule Takahiro Arakawa John A. C. Archer Peter Arner Magda Babina Sarah Rennie Piotr J. Balwierz Anthony G Beckhouse Swati Pradhan-Bhatt Judith A. Blake Antje Blumenthal Beatrice Bodega Alessandro Bonetti James Briggs Frank Brombacher A. Maxwell Burroughs Andrea Califano Carlo Vittorio Cannistraci Daniel Carbajo Yun Chen Marco Chierici Yari Ciani Hans Clevers Emiliano Dalla Carrie Davis Michael Detmar Alexander D. Diehl Taeko Dohi Finn Drabløs Albert S.B. Edge Matthias Edinger Karl Ekwall Mitsuhiro Endoh Hideki Enomoto Michela Fagiolini Lynsey Fairbairn Hai Fang Mary C. Farach‐Carson Geoffrey J. Faulkner Alexander V. Favorov Malcolm E Fisher Martin C. Frith Rie Fujita Shiro Fukuda Cesare Furlanello Masaaki Furuno Jun Furusawa Teunis B. H. Geijtenbeek Andrew P. Gibson T Gingeras Dan Goldowitz Julian Gough Sven Guhl Reto Guler Stefano Gustincich Thomas J Ha Masahide Hamaguchi Mitsuko Hara Matthias Harbers Jayson Harshbarger Akira Hasegawa Yuki Hasegawa Takehiro Hashimoto Meenhard Herlyn Kelly J Hitchens Shannan J. Ho Sui Oliver Hofmann Ilka Hoof Fumi Hori Łukasz Huminiecki

10.1038/nature13182 article EN Nature 2014-03-01

Animal microRNA sequences are subject to 3′ nucleotide addition. Through detailed analysis of deep-sequenced short RNA data sets, we show adenylation and uridylation miRNA is globally present conserved across Drosophila vertebrates. To better understand function, after knockdown nucleotidyltransferase enzymes. The PAPD4 adenylates a wide range loci, but does not appear affect stability on genome-wide scale. Adenine addition appears reduce effectiveness targeting mRNA transcripts while...

10.1101/gr.106054.110 article EN cc-by-nc Genome Research 2010-08-18

While several studies have focused on the relationship between individual miRNA loci or classes of small RNA with human Argonaute (AGO) proteins, a comprehensive, global analysis content associating different AGO proteins has yet to be performed. We compared deep sequenced extracted from immunoprecipitation experiments AGO1, AGO2, and AGO3 proteins. Consistent previous observations, sequence tags derived globally associate in approximately equivalent amounts AGO3. Exceptions include miR-182,...

10.4161/rna.8.1.14300 article EN RNA Biology 2011-01-01

Abstract Background The major role of enzymatic toxins that target nucleic acids in biological conflicts at all levels has become increasingly apparent thanks large part to the advances comparative genomics. Typically, evolve rapidly hampering identification these proteins by sequence analysis. Here we analyze an unexpectedly widespread superfamily toxin domains most which possess RNase activity. Results HEPN is comprised α-helical were first identified as being associated with DNA...

10.1186/1745-6150-8-15 article EN cc-by Biology Direct 2013-06-15

Cyclic di- and linear oligo-nucleotide signals activate defenses against invasive nucleic acids in animal immunity; however, their evolutionary antecedents are poorly understood. Using comparative genomics, sequence structure analysis, we uncovered a vast network of systems defined by conserved prokaryotic gene-neighborhoods, which encode enzymes generating such nucleotides or alternatively processing them to yield potential signaling molecules. The nucleotide-generating include several...

10.1093/nar/gkv1267 article EN cc-by-nc Nucleic Acids Research 2015-11-20

Ubiquitin (Ub)-mediated signaling is one of the hallmarks all eukaryotes. Prokaryotic homologs Ub (ThiS and MoaD) E1 ligases have been studied in relation to sulfur incorporation reactions thiamine molybdenum/tungsten cofactor biosynthesis. However, there no evidence for entire protein modification systems with Ub-like proteins deconjugation by deubiquitinating enzymes prokaryotes. Hence, evolutionary assembly eukaryotic Ub-signaling apparatus remains unclear.We systematically analyzed...

10.1186/gb-2006-7-7-r60 article EN cc-by Genome biology 2006-07-19

Next-generation sequencing experiments have shown that microRNAs (miRNAs) are expressed in many different isoforms (isomiRs), whose biological relevance is often unclear. We found mature miR-21, the most widely researched miRNA because of its importance human disease, produced two prevalent isomiR forms differ by 1 nt at their 3' end, and moreover end miR-21 posttranscriptionally adenylated noncanonical poly(A) polymerase PAPD5. PAPD5 knockdown caused an increase expression level, suggesting...

10.1073/pnas.1317751111 article EN Proceedings of the National Academy of Sciences 2014-07-21

Discovery of the TET/JBP family dioxygenases that modify bases in DNA has sparked considerable interest novel base modifications and their biological roles. Using sensitive sequence structure analyses combined with contextual information from comparative genomics, we computationally characterize over 12 biochemical systems for modifications. We predict previously unidentified enzymes, such as kinetoplastid J-base generating glycosyltransferase (and its homolog GREB1), catalytic specificity...

10.1093/nar/gkt573 article EN cc-by-nc Nucleic Acids Research 2013-06-27
Hiromasa Morikawa Naganari Ohkura Alexis Vandenbon Masayoshi Itoh Sayaka Nagao-Sato and 95 more Hideya Kawaji Timo Lassmann Piero Carninci Yoshihide Hayashizaki Alistair R. R. Forrest Daron M. Standley Hiroshi Date Shimon Sakaguchi Alistair R. R. Forrest Hideya Kawaji Michael Rehli J. Kenneth Baillie Michiel de Hoon Vanja Haberle Timo Lassmann Ivan V. Kulakovskiy Marina Lizio Masayoshi Itoh Robin Andersson Chris Mungall Terrence F. Meehan Sebastian Schmeier Nicolas Bertin Mette Jørgensen Emmanuel Dimont Peter Arner Christian Schmidl Ulf Schaefer Yulia A. Medvedeva Charles Plessy Morana Vitezic Jessica Severin Colin A. Semple Yuri Ishizu Margherita Francescatto Intikhab Alam Davide Albanese Gabriel Altschuler John A. C. Archer Peter Arner Magda Babina Sarah Baker Piotr J. Balwierz Anthony G Beckhouse Swati Pradhan-Bhatt Judith A. Blake Antje Blumenthal Beatrice Bodega Alessandro Bonetti James Briggs Frank Brombacher A. Maxwell Burroughs Andrea Califano Carlo Vittorio Cannistraci Daniel Carbajo Yun Chen Marco Chierici Yari Ciani Hans Clevers Emiliano Dalla Carrie Davis Bart Deplancke Michael Detmar Alexander D. Diehl Taeko Dohi Finn Drabløs Albert S.B. Edge Matthias Edinger Karl Ekwall Mitsuhiro Endoh Hideki Enomoto Michela Fagiolini Lynsey Fairbairn Hai Fang Mary C. Farach‐Carson Geoffrey J. Faulkner Alexander V. Favorov Malcolm E Fisher Martin C. Frith Rie Fujita Shiro Fukuda Cesare Furlanello Masaaki Furuno Jun-ichi Furusawa Teunis B. H. Geijtenbeek Andrew Gibson T Gingeras Dan Goldowitz Julian Gough Sven Guhl Reto Guler Stefano Gustincich Thomas J Ha Masahide Hamaguchi Mitsuko Hara

Naturally occurring regulatory T (Treg) cells, which specifically express the transcription factor forkhead box P3 (Foxp3), are engaged in maintenance of immunological self-tolerance and homeostasis. By transcriptional start site cluster analysis, we assessed here how genome-wide patterns DNA methylation or Foxp3 binding sites were associated with Treg-specific gene expression. We found that hypomethylated regions closely Treg up-regulated clusters, whereas had no significant correlation...

10.1073/pnas.1312717110 article EN Proceedings of the National Academy of Sciences 2014-03-27

Jumbo phages have attracted much attention by virtue of their extraordinary genome size and unusual aspects biology. By performing a comparative genomics analysis 224 jumbo phages, we suggest an objective inclusion criterion based on distributions present synthetic overview manifold adaptations across major biological systems. means clustering principal component the phyletic patterns conserved genes, all known can be classified into three higher-order groups, which include both myoviral...

10.3390/v13010063 article EN cc-by Viruses 2021-01-05

Recent studies have shown that the ubiquitin system had its origins in ancient cofactor/amino acid biosynthesis pathways. Preliminary also indicated conjugation systems for other peptide tags on proteins, such as pupylation, evolutionary links to Following up these observations, we systematically investigated non-ribosomal amidoligases of ATP-grasp, glutamine synthetase-like and acetyltransferase folds by classifying known members identifying novel versions. We then established their...

10.1039/b917682a article EN Molecular BioSystems 2009-01-01

Spliceostatin A (SSA) is a methyl ketal derivative of FR901464, potent antitumor compound isolated from culture broth Pseudomonas sp . no. 2663. These compounds selectively bind to the essential spliceosome component SF3b, subcomplex U2 snRNP, inhibit pre-mRNA splicing. However, mechanism SSA's activity unknown. It noteworthy that SSA causes accumulation truncated form CDK inhibitor protein p27 translated CDKN1B pre-mRNA, which involved in SSA-induced cell-cycle arrest. it still unclear...

10.1261/rna.058065.116 article EN RNA 2016-10-17

Both prokaryotic and eukaryotic immune systems face the dangers of premature activation effectors degradation self-molecules in absence an invader. To mitigate this, they have evolved threshold-setting regulatory mechanisms for triggering only upon detection a sufficiently strong invader signal. This work defines general templates such regulation effector-based systems. Using we identify several previously uncharacterized that accomplish downstream effector deployment by using nucleotide,...

10.1128/jb.00365-20 article EN Journal of Bacteriology 2020-09-01
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