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Genomes and Genes | bratSummaryGene Symbol: brat Description: brain tumor Alias: BRAT, Brat, CG10719, Dmel\CG10719, E60, anon-37CDa, fs(2)ltoPM43, l(2)37Cf, l(2)E60, l(2)brat, CG10719-PA, CG10719-PB, CG10719-PC, CG10719-PE, brain tumour, brat-PA, brat-PB, brat-PC, brat-PE Species: fruit fly Top Publications
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Publications
The brain tumor gene negatively regulates neural progenitor cell proliferation in the larval central brain of DrosophilaBruno Bello
Biozentrum, University of Basel, Klingelbergstrasse 50, CH 4056 Basel, Switzerland
Development 133:2639-48. 2006..in brat mutant clones promotes cell cycle exit and differentiation of brat mutant cells, thereby abrogating brain tumour formation...
The Drosophila melanogaster gene brain tumor negatively regulates cell growth and ribosomal RNA synthesisDeborah J Frank
Division of Basic Sciences and Molecular and Cellular Biology Program, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA
Development 129:399-407. 2002..We now indicate that the Drosophila melanogaster tumor suppressor brain tumor (brat) is an inhibitor of cell growth and is a functional homolog of the C. elegans gene ncl-1...
Pumilio binds para mRNA and requires Nanos and Brat to regulate sodium current in Drosophila motoneuronsNara I Muraro
Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, United Kingdom
J Neurosci 28:2099-109. 2008..the cofactor Nanos is essential for Pum-dependent para repression, whereas the requirement for Brain Tumor (Brat) is cell type specific...
Asymmetric segregation of the tumor suppressor brat regulates self-renewal in Drosophila neural stem cellsJoerg Betschinger
Institute of Molecular Biotechnology of the Austrian Academy of Sciences IMBA, Dr Bohr Gasse 3 5, 1030 Vienna, Austria
Cell 124:1241-53. 2006..neuroblasts-stem cell-like precursors of the adult brain-regulate proliferation by segregating the growth inhibitor Brat and the transcription factor Prospero into only one daughter cell...
Mutations in the beta-propeller domain of the Drosophila brain tumor (brat) protein induce neoplasm in the larval brainE Arama
Department of Biology, Technion Israel Institute of Technology, Haifa
Oncogene 19:3706-16. 2000Inactivation of both alleles of the fruit fly D. melanogaster brain tumor (brat) gene results in the production of a tumor-like neoplasm in the larval brain, and lethality in the larval third instar and pupal stages...
Drosophila Brain Tumor is a translational repressorJ Sonoda
Howard Hughes Medical Institute, Department of Genetics, Duke University Medical Center, Durham, North Carolina 27710, USA
Genes Dev 15:762-73. 2001The Drosophila brain tumor (brat) gene encodes a member of the conserved NHL family of proteins, which appear to regulate differentiation and growth in a variety of organisms...
Cap-dependent translational inhibition establishes two opposing morphogen gradients in Drosophila embryosPark F Cho
Department of Biochemistry and McGill Cancer Center, McGill University, 3655 Promenade Sir William Osler, Montreal, Quebec H3G 1Y6, Canada
Curr Biol 16:2035-41. 2006..requires an mRNP complex (the NRE complex), which consists of Nanos (Nos), Pumilio (Pum), and Brain tumor (Brat) proteins, and the Nos responsive element (NRE) present in the 3' UTR of hb mRNA ...
The mei-P26 gene encodes a RING finger B-box coiled-coil-NHL protein that regulates seizure susceptibility in DrosophiliaEdward Glasscock
Department of Molecular and Cell Biology, Division of Neurobiology, University of California, Berkeley, CA 94720, USA
Genetics 170:1677-89. 2005..These results reveal a surprising role for mei-P26 outside of the germline as a regulator of seizure susceptibility, possibly by affecting synaptic development as a ubiquitin ligase...
Drosophila brain tumor metastases express both neuronal and glial cell type markersMichelle Beaucher
Department of Biology, The Johns Hopkins University, Baltimore, MD 21218, USA
Dev Biol 301:287-97. 2007Loss of either lgl or brat gene activity in Drosophila larvae causes neoplastic brain tumors. Fragments of tumorous brains from either mutant transplanted into adult hosts over-proliferate, and kill their hosts within 2 weeks...
Aurora-A acts as a tumor suppressor and regulates self-renewal of Drosophila neuroblastsHongyan Wang
Temasek Life Sciences Laboratory and Department of Biological Sciences, National University of Singapore, Singapore 117604
Genes Dev 20:3453-63. 2006..We have identified a novel mechanism for controlling the balance between self-renewal and neuronal differentiation during the asymmetric division of Drosophila larval NBs...
The Drosophila NuMA Homolog Mud regulates spindle orientation in asymmetric cell divisionSarah K Bowman
Institute of Molecular Biotechnology of the Austrian Academy of Sciences IMBA, Dr Bohr Gasse 3 5, 1030 Vienna, Austria
Dev Cell 10:731-42. 2006..This can lead to symmetric segregation of the cell fate determinants Brat and Prospero, resulting in the mis-specification of daughter cell fates and tumor-like over proliferation in the ..
Drosophila Aurora-A kinase inhibits neuroblast self-renewal by regulating aPKC/Numb cortical polarity and spindle orientationCheng Yu Lee
Institutes of Neuroscience and Molecular Biology, Howard Hughes Medical Institute, University of Oregon, Eugene, Oregon 97403, USA
Genes Dev 20:3464-74. 2006..We conclude that Aurora-A and Numb are novel inhibitors of neuroblast self-renewal and that spindle orientation regulates neuroblast self-renewal...
Connecting cancer to the asymmetric division of stem cellsAndreas Wodarz
Department of Stem Cell Biology, DFG Research Center for Molecular Physiology of the Brain CMPB, University of Gottingen, Justus von Liebig Weg 11, 37077 Gottingen, Germany
Cell 124:1121-3. 2006..one in this issue of Cell and the other in Developmental Cell show that the cell-fate determinant Brain Tumor (Brat) suppresses self-renewal in one of the daughter cells that arise from the asymmetric division of a neural stem cell...
Metastatic ability of Drosophila tumors depends on MMP activityMichelle Beaucher
Department of Biology, The Johns Hopkins University, Baltimore, MD 21218, USA
Dev Biol 303:625-34. 2007We analyzed how cells from tumors caused by mutations in either lgl or brat use matrix metalloproteinases (MMPs) to facilitate metastasis in Drosophila...
Polo inhibits progenitor self-renewal and regulates Numb asymmetry by phosphorylating PonHongyan Wang
Temasek Life Sciences Laboratory and Department of Biological Sciences, National University of Singapore, Singapore 117604
Nature 449:96-100. 2007..Our results reveal a biochemical link between the cell cycle and the asymmetric protein localization machinery, and indicate that Polo can inhibit progenitor self-renewal by regulating the localization and function of Numb...
Brat promotes stem cell differentiation via control of a bistable switch that restricts BMP signalingRobin E Harris
Faculty of Life Sciences, University of Manchester, Oxford Road, Manchester M13 9PT, UK
Dev Cell 20:72-83. 2011..Here, we identify Brain Tumor (Brat) as a potent differentiation factor and target of Pum-Nos regulation...
A broadly conserved pathway generates 3'UTR-directed primary piRNAsNicolas Robine
Department of Developmental Biology, Sloan Kettering Institute, New York, NY 10065, USA
Curr Biol 19:2066-76. 2009..Certain stages of mammalian testis also accumulate abundant piRNAs of unknown function, which derive from noncoding RNAs that are depleted in transposable element content and do not engage in ping-pong...
The exosome associates cotranscriptionally with the nascent pre-mRNP through interactions with heterogeneous nuclear ribonucleoproteinsViktoria Hessle
Department of Molecular Biology and Functional Genomics, Stockholm University, SE 10691 Stockholm, Sweden
Mol Biol Cell 20:3459-70. 2009..Our results lead to a revised mechanistic model for cotranscriptional quality control in which the exosome is constantly recruited to newly synthesized RNAs through direct interactions with specific hnRNP proteins...
Modulated modularity clustering as an exploratory tool for functional genomic inferenceEric A Stone
Department of Statistics, North Carolina State University, Raleigh, NC, USA
PLoS Genet 5:e1000479. 2009..We show MMC to be effective and suitable to applications of large scale. In light of these features, we advocate MMC as a standard tool for exploration and hypothesis generation...
Protein phosphatase 4 mediates localization of the Miranda complex during Drosophila neuroblast asymmetric divisionsRita Sousa-Nunes
Department of Biological Sciences, Temasek Life Sciences Laboratory, National University of Singapore, Singapore
Genes Dev 23:359-72. 2009..Our findings suggest that Flfl may target PP4 to the MIra protein complex to facilitate dephosphorylation step(s) crucial for its cortical association/asymmetric localization...
A conserved nuclear receptor, Tailless, is required for efficient proliferation and prolonged maintenance of mushroom body progenitors in the Drosophila brainMitsuhiko Kurusu
Structural Biology Center, National Institute of Genetics, and Department of Genetics, The Graduate University for Advanced Studies, 1111 Yata, Mishima, Shizuoka 411 8540, Japan
Dev Biol 326:224-36. 2009..These results as a whole uncover a distinct regulatory mechanism of self-renewal and differentiation of the MB progenitors that is different from the mechanisms found in other progenitors...
The PDZ protein Canoe regulates the asymmetric division of Drosophila neuroblasts and muscle progenitorsStephan Speicher
Instituto de Neurociencias de Alicante, Consejo Superior de Investigaciones Científicas University Miguel Hernandez, Sant Joan d Alacant, 03550 Alicante, Spain
Curr Biol 18:831-7. 2008....
The tumor suppressors Brat and Numb regulate transit-amplifying neuroblast lineages in DrosophilaSarah K Bowman
Institute of Molecular Biotechnology of the Austrian Academy of Sciences, Dr Bohr Gasse 3, 1030 Vienna, Austria
Dev Cell 14:535-46. 2008..PAN neuroblasts rely on the segregating determinants Numb and Brat to generate smaller, secondary neuroblasts that in turn give rise to ganglion mother cells (GMCs) and neurons ..
Regulation of the Drosophila lin-41 homologue dappled by let-7 reveals conservation of a regulatory mechanism within the LIN-41 subcladeFergal O'Farrell
Department of Natural Sciences, Södertörns högskola, Huddinge, Sweden
Dev Dyn 237:196-208. 2008..A cell-based assay verified let-7 miRNA down-regulation of dpld expression by means of its 3'-untranslated region. Thus, dpld seems also to be miRNA regulated, suggesting that miRNAs represent an ancient mechanism of LIN-41 regulation...
Asymmetric localisation of Miranda and its cargo proteins during neuroblast division requires the anaphase-promoting complex/cyclosomeCathy Slack
MRC Centre for Developmental Neurobiology, New Hunt s House, King s College London, Guy s Campus, London SE1 1UL, UK
Development 134:3781-7. 2007..the asymmetric localisation of the adapter protein Miranda and its associated cargo proteins Staufen, Prospero and Brat, but not other components of the asymmetric division machinery...
Brat is a Miranda cargo protein that promotes neuronal differentiation and inhibits neuroblast self-renewalCheng Yu Lee
Institutes of Neuroscience and Molecular Biology, Howard Hughes Medical Institute, University of Oregon, Eugene, 97403, USA
Dev Cell 10:441-9. 2006..Here, we report that the Brain tumor (Brat) translation repressor is partitioned into GMCs via direct interaction with the Miranda scaffolding protein...
The myb-related gene stonewall induces both hyperplasia and cell death in Drosophila: rescue of fly lethality by coexpression of apoptosis inducersS Brun
Laboratoire de Genetique et Biologie Cellulaire, CNRS MR 8159, Universite de Versailles St Quentin en Yvelines, 45 Avenue des Etats Unis, F 78035 Versailles cedex, France
Cell Death Differ 13:1752-62. 2006..Our results suggest that stwl(UY823) kills flies by causing inappropriate cell cycle entry, and that triggering the death of these overproliferating cells or slowing their proliferation restores viability...
Induction of tumor growth by altered stem-cell asymmetric division in Drosophila melanogasterEmmanuel Caussinus
Cell Biology and Biophysics Program, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany
Nat Genet 37:1125-9. 2005....
Growth, metastasis, and invasiveness of Drosophila tumors caused by mutations in specific tumor suppressor genesE Woodhouse
Department of Biology, The Johns Hopkins University, Baltimore, Maryland 21218, USA
Dev Genes Evol 207:542-50. 1998....
derailed is required for muscle attachment site selection in DrosophilaC A Callahan
Molecular Neurobiology Laboratory, The Salk Institute for Biological Studies, San Diego, CA 92186, USA
Development 122:2761-7. 1996..The data suggest that both neurons and muscles use common mechanisms to recognize their paths or targets, and that Drl plays an analogous role in both developing systems...
The Wilhelmine E. Key 1992 Invitational lecture. Phenotypic analysis of the Dopa decarboxylase gene cluster mutants in Drosophila melanogasterT R Wright
University of Virginia, Department of Biology, Charlottesville 22903 2477, USA
J Hered 87:175-90. 1996..Thus, the Ddc gene cluster represents in higher eukaryotes an unusual example of a large cluster of functionally related genes involved in a common physiological process...
The genetic and molecular organization of the Dopa decarboxylase gene cluster of Drosophila melanogasterD G Stathakis
Department of Biology, University of Virginia, Charlottesville 22903 2477, USA
Genetics 141:629-55. 1995....
Effects of Ddc cluster lethal alleles on ovary growth, attachment, and egg production in DrosophilaE McCrady
Department of Biology, University of North Carolina at Greensboro 27412
J Exp Zool 268:469-76. 1994..Heteroallelic heterozygotes of Bd7 x Bd4 also produced fully fertile ovaries, but no other heteroallelic combinations did so.(ABSTRACT TRUNCATED AT 250 WORDS)..
The genetics of dopa decarboxylase in Drosophila melanogaster. IV. The genetics and cytology of the 37B10-37D1 regionT R Wright
Chromosoma 83:45-58. 1981..It eliminates Ddc+ and 1(2)37Ca+ function and at 30 degrees C reduces 1(2)37Ce+ function. It is not a deficiency but could be a polar mutant...
Molecular mapping of a gene cluster flanking the Drosophila Dopa decarboxylase geneD Gilbert
Genetics 106:679-94. 1984..Six of these complementation groups are within 23 kb of DNA, and all ten complementation groups, including Ddc, lie within 78-82 kb of DNA. The potential significance of this unusually high gene density is discussed...
A diphenol oxidase gene is part of a cluster of genes involved in catecholamine metabolism and sclerotization in Drosophila. II. Molecular localization of the Dox-A2 coding regionE S Pentz
Genetics 112:843-59. 1986..The Dox-A2 locus is within 3.4 to 4.4 kb of the Df(2L)OD15 breakpoint, placing four of the vital loci within a maximum of 15.5 kb. The location of Dox-A2 in a cluster of genes affecting cuticle formation is discussed...
Tumor-suppressor genes of Drosophila melanogasterE Gateff
Institute of Genetics, Johannes Gutenberg University, Mainz, West Germany
Crit Rev Oncog 1:221-45. 1989
The genetics of dopa decarboxylase in Drosophila melanogaster. II. Isolation and characterization of dopa-decarboxylase-deficient mutants and their relationship to the alpha-methyl-dopa-hypersensitive mutantsT R Wright
Genetics 84:287-310. 1976..Although no biochemical phene has yet been established for the alphaMD hypersensitive amd alleles, it seems likely that the two groups of mutants are functionally related...
Dual-tagging gene trap of novel genes in Drosophila melanogasterT Lukacsovich
School of Human Sciences and Advanced Research Institute for Science and Engineering, Waseda University, Saitama 359 1192, Japan
Genetics 157:727-42. 2001....
Control of neuronal pathway selection by a Drosophila receptor protein-tyrosine kinase family memberC A Callahan
Molecular Neurobiology Laboratory, Salk Institute for Biological Studies, San Diego, California 92186, USA
Nature 376:171-4. 1995..In drl mutant embryos these neurons fail to make the correct pathway choices. Our results provide evidence for receptor protein-tyrosine kinase involvement in key aspects of neuronal pathway recognition...
How cells coordinate growth and divisionPaul Jorgensen
Department of Medical Genetics and Microbiology, University of Toronto, Toronto ON, Canada M5S 1A8
Curr Biol 14:R1014-27. 2004..Recently, genetic screens in Drosophila and functional genomics approaches in yeast have macheted into the thicket of cell size control...
Model of the brain tumor-Pumilio translation repressor complexThomas A Edwards
Department of Physiology and Biophysics, Mount Sinai School of Medicine, New York, New York 10029, USA
Genes Dev 17:2508-13. 2003The Brain Tumor (Brat) protein is recruited to the 3' untranslated region (UTR) of hunchback mRNA to regulate its translation...
Translational repressors in DrosophilaKellie A Dean
Howard Hughes Medical Institute, Dept of Molecular Genetics and Microbiology, Box 3657, Duke University Medical Center, Durham, NC 27710, USA
Trends Genet 18:572-7. 2002..These repressors do not work in isolation - each binds multiple sites in the appropriate mRNA, and the resulting RNA-protein complexes appear to recruit co-repressors by a variety of mechanisms...
Control of developmental timing by micrornas and their targetsAmy E Pasquinelli
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02114, USA
Annu Rev Cell Dev Biol 18:495-513. 2002..Instead of inventing new gene functions, even subtle changes in temporal expression of pre-existing control genes can result in speciation by altering the time at which they function...
A PUF family portrait: 3'UTR regulation as a way of lifeMarvin Wickens
Dept of Biochemistry, University of Wisconsin, Madison, WI 53706, USA
Trends Genet 18:150-7. 2002..Here, we discuss the evolution, biological function and mechanisms of action of the PUF protein family, and suggest that a primordial function of PUF proteins is to sustain mitotic proliferation of stem cells...
Development. The message is in the translationJ D Richter
Department of Molecular Genetics and Microbiology, University of Massachusetts Medical School, Worcester, MA 01605, USA
Science 293:60-2. 2001
Structure of Pumilio reveals similarity between RNA and peptide binding motifsT A Edwards
Structural Biology Program, Department of Physiology and Biophysics, Mount Sinai School of Medicine, Box 1677, 1425 Madison Avenue, New York, NY 10029, USA
Cell 105:281-9. 2001..This analysis suggests that similar features in helical repeat proteins are used to bind extended peptides and RNA...
Nuclear import of activated D-ERK by DIM-7, an importin family member encoded by the gene moleskinJ A Lorenzen
Pediatric Surgical Research Laboratories, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA
Development 128:1403-14. 2001..Mutations in the Drosophila Importin beta homolog Ketel, also reduce the nuclear localization of activated D-ERK. Together, these data indicate that DIM-7 and Ketel are components of the nuclear import machinery for activated D-ERK...
The fruit fly Drosophila and the fish Xiphophorus as model systems for cancer studiesB Mechler
Department of Development Genetics, Deutsches Krebsforschungszentrum, German Cancer Research Center, Heidelberg
Cancer Surv 9:505-27. 1990..This gene encodes a receptor tyrosine kinase related to the EGF-receptor, and its activation and overexpression are thought to play a critical part in melanoma formation...
Research Grants
- Function of 3'UTRsMARVIN P WICKENS; Fiscal Year: 2011..These proteins control stem cells and participate in the formation of memory. Understanding how they work should provide practical opportunities for intervention. ..
- RNA Localization 2006Joel Richter; Fiscal Year: 2007..The cross-disciplinary nature of this meeting will be attractive to molecular, cellular, developmental, and neurobiological scientists. ..
- TRANSLATIONAL CONTROL IN EARLY MAMMALIAN DEVELOPMENTJoel Richter; Fiscal Year: 2007..The importance of CPEB3 for oocytedevelopment will be assessed. The proposed experiments will examine the molecular basis of oocyte development, and thus are relevant to human health especially human reproduction. ..
- CPEB and Cell SenescenceJoel Richter; Fiscal Year: 2007..This proposal focuses on new molecules that regulate cell senescence. Because this process is strongly linked to cancer and ageing, it clearly has important implications for human health. ..
- CELL BIOLOGY OF DEVELOPMENTJoel Richter; Fiscal Year: 2007....
- POLYADENYLATION AND TRANSLATIONAL CONTROLJoel Richter; Fiscal Year: 2007..Therefore, mechanistic studies of polyadenylation-induced translation are likely to have important implications for human health. ..
- CLEAVAGE, POLYADENYLATION, AND TRANSPORT OF MRNAMarvin Wickens; Fiscal Year: 2007..In focusing sharply on a few specific examples, we hope to illuminate the broad molecular questions of how 3'UTR controls function, evolve, and coordinate exoression of multiole mRNAs. ..
- Function of 3' UTRsMarvin Wickens; Fiscal Year: 2007..We focus sharply on PUF proteins to illuminate broadly how 3'UTR controls function, evolve, and coordinate expression of multiple mRNAs. ..
- CPEB and Cell SenescenceJoel D Richter; Fiscal Year: 2010..This proposal focuses on new molecules that regulate cell senescence. Because this process is strongly linked to cancer and ageing, it clearly has important implications for human health. ..
- POLYADENYLATION AND TRANSLATIONAL CONTROLJoel D Richter; Fiscal Year: 2010..In particular, we will examine RNA processing and translational control. Because of the fundamental nature of this work, it has important implications for fertility, neurodegeneration, and cancer. ..
- Function of 3'UTRsMARVIN P WICKENS; Fiscal Year: 2010..These proteins control stem cells and participate in the formation of memory. Understanding how they work should provide practical opportunities for intervention. ..
- POLYADENYLATION AND TRANSLATIONAL CONTROLJoel Richter; Fiscal Year: 2009..Finally, an upstream event that is necessary for CPEB-mediated polyadenylation is the translational activation of RINGO/Spy mRNA, which encodes an atypical cyclin B1-like protein. Pumilio is the ..
- CPEB and Cell SenescenceJoel Richter; Fiscal Year: 2009..This proposal focuses on new molecules that regulate cell senescence. Because this process is strongly linked to cancer and ageing, it clearly has important implications for human health. ..
- POLYADENYLATION AND TRANSLATIONAL CONTROLJoel Richter; Fiscal Year: 2009..In particular, we will examine RNA processing and translational control. Because of the fundamental nature of this work, it has important implications for fertility, neurodegeneration, and cancer. ..
- POLYADENYLATION AND TRANSLATIONAL CONTROLJoel Richter; Fiscal Year: 1999....
- POLYADENYLATION AND TRANSLATIONAL CONTROLJoel Richter; Fiscal Year: 2003..The mechanism responsible for, and the biological significance of, this localization will be investigated. ..
- FUNCTION OF 3 UTRSMarvin Wickens; Fiscal Year: 2002..Our detailed investigations of the regulation of c-mos, a proto-oncogene normally expressed only in the germ line, bear on how cell division is controlled both in normal and abnormal growth. ..
- TRANSLATIONAL CONTROL IN EARLY MAMMALIAN DEVELOPMENTJoel Richter; Fiscal Year: 2001..Finally, an mRNA that is deadenylated and stored in a dormant form in mouse oocytes undergoes prior CPE-mediated deadenylation. The possible role of mCPEB in the process will be assessed. ..
