Regenerative Growth in Drosophila Imaginal Discs Is Regulated by Wingless and Myc

The study of regeneration would be aided greatly by systems that support large-scale genetic screens. Here we describe a nonsurgical method for inducing tissue damage and regeneration in Drosophila larvae by inducing apoptosis in the wing imaginal disc in a spatially and temporally regulated manner....

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Published inDevelopmental cell Vol. 16; no. 6; pp. 797 - 809
Main Authors Smith-Bolton, Rachel K., Worley, Melanie I., Kanda, Hiroshi, Hariharan, Iswar K.
Format Journal Article
LanguageEnglish
Published Cambridge, MA Elsevier Inc 01.06.2009
Cell Press
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Abstract The study of regeneration would be aided greatly by systems that support large-scale genetic screens. Here we describe a nonsurgical method for inducing tissue damage and regeneration in Drosophila larvae by inducing apoptosis in the wing imaginal disc in a spatially and temporally regulated manner. Tissue damage results in localized regenerative proliferation characterized by altered expression of patterning genes and growth regulators as well as a temporary loss of markers of cell fate commitment. Wingless and Myc are induced by tissue damage and are important for regenerative growth. Furthermore, ectopic Myc enhances regeneration when other growth drivers tested do not. As the animal matures, the ability to regenerate is lost and cannot be restored by activation of Wingless or Myc. This system is conducive to forward genetic screens, enabling an unbiased search for genes that regulate both the extent of and the capacity for regeneration.
AbstractList The study of regeneration would be aided greatly by systems that support large-scale genetic screens. Here we describe a nonsurgical method for inducing tissue damage and regeneration in Drosophila larvae by inducing apoptosis in the wing imaginal disc in a spatially and temporally regulated manner. Tissue damage results in localized regenerative proliferation characterized by altered expression of patterning genes and growth regulators as well as a temporary loss of markers of cell fate commitment. Wingless and Myc are induced by tissue damage and are important for regenerative growth. Furthermore, ectopic Myc enhances regeneration when other growth drivers tested do not. As the animal matures, the ability to regenerate is lost and cannot be restored by activation of Wingless or Myc. This system is conducive to forward genetic screens, enabling an unbiased search for genes that regulate both the extent of and the capacity for regeneration.
The study of regeneration would be aided greatly by systems that support large-scale genetic screens. Here we describe a nonsurgical method for inducing tissue damage and regeneration in Drosophila larvae by inducing apoptosis in the wing imaginal disc in a spatially and temporally regulated manner. Tissue damage results in localized regenerative proliferation characterized by altered expression of patterning genes and growth regulators as well as a temporary loss of markers of cell fate commitment. Wingless and Myc are induced by tissue damage and are important for regenerative growth. Furthermore, ectopic Myc enhances regeneration when other growth drivers tested do not. As the animal matures, the ability to regenerate is lost and cannot be restored by activation of Wingless or Myc. This system is conducive to forward genetic screens, enabling an unbiased search for genes that regulate both the extent of and the capacity for regeneration.
The study of regeneration would be aided greatly by systems that support large-scale genetic screens. Here we describe a non-surgical method for inducing tissue damage and regeneration in Drosophila larvae by inducing apoptosis in the wing imaginal disc in a spatially and temporally regulated manner. Tissue damage results in localized regenerative proliferation characterized by altered expression of patterning genes and growth regulators as well as a temporary loss of markers of cell fate commitment. Wingless and Myc are induced by tissue damage and are important for regenerative growth. Furthermore, ectopic Myc enhances regeneration when other growth drivers tested do not. As the animal matures, the ability to regenerate is lost and cannot be restored by activation of Wg or Myc. This system is conducive to forward genetic screens, enabling an unbiased search for genes that regulate both the extent of and the capacity for regeneration.
Author Smith-Bolton, Rachel K.
Worley, Melanie I.
Kanda, Hiroshi
Hariharan, Iswar K.
AuthorAffiliation 1 Department of Molecular and Cell Biology, University of California, Berkeley. Berkeley, CA 94720, USA
AuthorAffiliation_xml – name: 1 Department of Molecular and Cell Biology, University of California, Berkeley. Berkeley, CA 94720, USA
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  surname: Worley
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  organization: Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA
– sequence: 3
  givenname: Hiroshi
  surname: Kanda
  fullname: Kanda, Hiroshi
  organization: Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA
– sequence: 4
  givenname: Iswar K.
  surname: Hariharan
  fullname: Hariharan, Iswar K.
  email: ikh@berkeley.edu
  organization: Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA
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Keywords DEVBIO
Growth
Arthropoda
Insecta
Development
Invertebrata
Onc gene
Drosophila melanogaster
Diptera
Drosophilidae
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Current address: Department of Physiology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan
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crossref_primary_10_1016_j_devcel_2009_04_015
pubmed_primary_19531351
pascalfrancis_primary_21640090
elsevier_sciencedirect_doi_10_1016_j_devcel_2009_04_015
PublicationCentury 2000
PublicationDate 20090601
PublicationDateYYYYMMDD 2009-06-01
PublicationDate_xml – month: 6
  year: 2009
  text: 20090601
  day: 1
PublicationDecade 2000
PublicationPlace Cambridge, MA
PublicationPlace_xml – name: Cambridge, MA
– name: United States
PublicationTitle Developmental cell
PublicationTitleAlternate Dev Cell
PublicationYear 2009
Publisher Elsevier Inc
Cell Press
Publisher_xml – name: Elsevier Inc
– name: Cell Press
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SSID ssj0016180
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Snippet The study of regeneration would be aided greatly by systems that support large-scale genetic screens. Here we describe a nonsurgical method for inducing tissue...
The study of regeneration would be aided greatly by systems that support large-scale genetic screens. Here we describe a non-surgical method for inducing...
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SubjectTerms Animals
Biological and medical sciences
Body Patterning
Cell differentiation, maturation, development, hematopoiesis
Cell Lineage
Cell physiology
Cell Proliferation
Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes
Cyclin E - metabolism
DEVBIO
DNA-Binding Proteins - metabolism
Drosophila melanogaster - cytology
Drosophila melanogaster - genetics
Drosophila melanogaster - growth & development
Drosophila melanogaster - metabolism
Drosophila Proteins - metabolism
Fundamental and applied biological sciences. Psychology
Genes, Insect
Intercellular Signaling Peptides and Proteins - metabolism
Larva - cytology
Larva - growth & development
Molecular and cellular biology
Mutation - genetics
Regeneration
Transcription Factors - metabolism
Up-Regulation - genetics
Wings, Animal - cytology
Wings, Animal - growth & development
Wings, Animal - metabolism
Wnt1 Protein - metabolism
Title Regenerative Growth in Drosophila Imaginal Discs Is Regulated by Wingless and Myc
URI https://dx.doi.org/10.1016/j.devcel.2009.04.015
https://www.ncbi.nlm.nih.gov/pubmed/19531351
https://search.proquest.com/docview/67387743
https://pubmed.ncbi.nlm.nih.gov/PMC2705171
Volume 16
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