Inheritance of Polycomb-dependent chromosomal interactions in Drosophila

Maintenance of cell identity is a complex task that involves multiple layers of regulation, acting at all levels of chromatin packaging, from nucleosomes to folding of chromosomal domains in the cell nucleus. Polycomb-group (PcG) and trithorax-group (trxG) proteins maintain memory of chromatin state...

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Published inGenes & development Vol. 17; no. 19; pp. 2406 - 2420
Main Authors Bantignies, Frédéric, Grimaud, Charlotte, Lavrov, Sergey, Gabut, Mathieu, Cavalli, Giacomo
Format Journal Article
LanguageEnglish
Published United States Cold Spring Harbor Laboratory Press 01.10.2003
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Abstract Maintenance of cell identity is a complex task that involves multiple layers of regulation, acting at all levels of chromatin packaging, from nucleosomes to folding of chromosomal domains in the cell nucleus. Polycomb-group (PcG) and trithorax-group (trxG) proteins maintain memory of chromatin states through binding at cis -regulatory elements named PcG response elements or cellular memory modules. Fab-7 is a well-defined cellular memory module involved in regulation of the homeotic gene Abdominal-B ( Abd-B ). In addition to its action in cis , we show here by three-dimensional FISH that the Fab-7 element leads to association of transgenes with each other or with the endogenous Fab-7 , even when inserted in different chromosomes. These long-distance interactions enhance PcG-mediated silencing. They depend on PcG proteins, on DNA sequence homology, and on developmental progression. Once long-distance pairing is abolished by removal of the endogenous Fab-7 , the derepressed chromatin state induced at the transgene locus can be transmitted through meiosis into a large fraction of the progeny, even after reintroduction of the endogenous Fab-7 . Strikingly, meiotic inheritance of the derepressed state involves loss of pairing between endogenous and transgenic Fab-7 . This suggests that transmission of nuclear architecture through cell division might contribute to inheritance of chromatin states in eukaryotes.
AbstractList Maintenance of cell identity is a complex task that involves multiple layers of regulation, acting at all levels of chromatin packaging, from nucleosomes to folding of chromosomal domains in the cell nucleus. Polycomb-group (PcG) and trithorax-group (trxG) proteins maintain memory of chromatin states through binding at cis -regulatory elements named PcG response elements or cellular memory modules. Fab-7 is a well-defined cellular memory module involved in regulation of the homeotic gene Abdominal-B ( Abd-B ). In addition to its action in cis , we show here by three-dimensional FISH that the Fab-7 element leads to association of transgenes with each other or with the endogenous Fab-7 , even when inserted in different chromosomes. These long-distance interactions enhance PcG-mediated silencing. They depend on PcG proteins, on DNA sequence homology, and on developmental progression. Once long-distance pairing is abolished by removal of the endogenous Fab-7 , the derepressed chromatin state induced at the transgene locus can be transmitted through meiosis into a large fraction of the progeny, even after reintroduction of the endogenous Fab-7 . Strikingly, meiotic inheritance of the derepressed state involves loss of pairing between endogenous and transgenic Fab-7 . This suggests that transmission of nuclear architecture through cell division might contribute to inheritance of chromatin states in eukaryotes.
Maintenance of cell identity is a complex task that involves multiple layers of regulation, acting at all levels of chromatin packaging, from nucleosomes to folding of chromosomal domains in the cell nucleus. Polycomb-group (PcG) and trithorax-group (trxG) proteins maintain memory of chromatin states through binding at cis-regulatory elements named PcG response elements or cellular memory modules. Fab-7 is a well-defined cellular memory module involved in regulation of the homeotic gene Abdominal-B (Abd-B). In addition to its action in cis, we show here by three-dimensional FISH that the Fab-7 element leads to association of transgenes with each other or with the endogenous Fab-7, even when inserted in different chromosomes. These long-distance interactions enhance PcG-mediated silencing. They depend on PcG proteins, on DNA sequence homology, and on developmental progression. Once long-distance pairing is abolished by removal of the endogenous Fab-7, the derepressed chromatin state induced at the transgene locus can be transmitted through meiosis into a large fraction of the progeny, even after reintroduction of the endogenous Fab-7. Strikingly, meiotic inheritance of the derepressed state involves loss of pairing between endogenous and transgenic Fab-7. This suggests that transmission of nuclear architecture through cell division might contribute to inheritance of chromatin states in eukaryotes.
Maintenance of cell identity is a complex task that involves multiple layers of regulation, acting at all levels of chromatin packaging, from nucleosomes to folding of chromosomal domains in the cell nucleus. Polycomb-group (PcG) and trithorax-group (trxG) proteins maintain memory of chromatin states through binding at cis-regulatory elements named PcG response elements or cellular memory modules. Fab-7 is a well-defined cellular memory module involved in regulation of the homeotic gene Abdominal-B (Abd-B). In addition to its action in cis, we show here by three-dimensional FISH that the Fab-7 element leads to association of transgenes with each other or with the endogenous Fab-7, even when inserted in different chromosomes. These long-distance interactions enhance PcG-mediated silencing. They depend on PcG proteins, on DNA sequence homology, and on developmental progression. Once long-distance pairing is abolished by removal of the endogenous Fab-7, the derepressed chromatin state induced at the transgene locus can be transmitted through meiosis into a large fraction of the progeny, even after reintroduction of the endogenous Fab-7. Strikingly, meiotic inheritance of the derepressed state involves loss of pairing between endogenous and transgenic Fab-7. This suggests that transmission of nuclear architecture through cell division might contribute to inheritance of chromatin states in eukaryotes.Maintenance of cell identity is a complex task that involves multiple layers of regulation, acting at all levels of chromatin packaging, from nucleosomes to folding of chromosomal domains in the cell nucleus. Polycomb-group (PcG) and trithorax-group (trxG) proteins maintain memory of chromatin states through binding at cis-regulatory elements named PcG response elements or cellular memory modules. Fab-7 is a well-defined cellular memory module involved in regulation of the homeotic gene Abdominal-B (Abd-B). In addition to its action in cis, we show here by three-dimensional FISH that the Fab-7 element leads to association of transgenes with each other or with the endogenous Fab-7, even when inserted in different chromosomes. These long-distance interactions enhance PcG-mediated silencing. They depend on PcG proteins, on DNA sequence homology, and on developmental progression. Once long-distance pairing is abolished by removal of the endogenous Fab-7, the derepressed chromatin state induced at the transgene locus can be transmitted through meiosis into a large fraction of the progeny, even after reintroduction of the endogenous Fab-7. Strikingly, meiotic inheritance of the derepressed state involves loss of pairing between endogenous and transgenic Fab-7. This suggests that transmission of nuclear architecture through cell division might contribute to inheritance of chromatin states in eukaryotes.
Author Grimaud, Charlotte
Lavrov, Sergey
Cavalli, Giacomo
Bantignies, Frédéric
Gabut, Mathieu
AuthorAffiliation 1 Institute of Human Genetics, Centre National de la Recherche Scientifique, 34396 Montpellier Cedex5, France
AuthorAffiliation_xml – name: 1 Institute of Human Genetics, Centre National de la Recherche Scientifique, 34396 Montpellier Cedex5, France
Author_xml – sequence: 1
  givenname: Frédéric
  surname: Bantignies
  fullname: Bantignies, Frédéric
– sequence: 2
  givenname: Charlotte
  surname: Grimaud
  fullname: Grimaud, Charlotte
– sequence: 3
  givenname: Sergey
  surname: Lavrov
  fullname: Lavrov, Sergey
– sequence: 4
  givenname: Mathieu
  surname: Gabut
  fullname: Gabut, Mathieu
– sequence: 5
  givenname: Giacomo
  surname: Cavalli
  fullname: Cavalli, Giacomo
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Present address: Institute of Molecular Genetics, CNRS, UMR-5535, 1919, Route de Mende, 34293 Montpellier, France.
Corresponding author. E-MAIL Giacomo.Cavalli@igh.cnrs.fr ; FAX 33-499-61-99-01.
Supplemental material is available at http://www.genesdev.org.
Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.269503.
Present address: DMGC, Institute of Molecular Genetics, RAS, 2, Kurchatovsq., Moscow, 123182, Russia
OpenAccessLink http://genesdev.cshlp.org/content/17/19/2406.full.pdf
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Snippet Maintenance of cell identity is a complex task that involves multiple layers of regulation, acting at all levels of chromatin packaging, from nucleosomes to...
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SubjectTerms Abdominal-B gene
Animals
Animals, Genetically Modified
Cell Nucleus - genetics
Chromatin - genetics
Chromosomes - genetics
DNA-Binding Proteins - genetics
Drosophila
Drosophila - embryology
Drosophila - genetics
Drosophila Proteins - genetics
Embryo, Nonmammalian
epigenetics
Fab-7 gene
Female
Gene Expression Regulation, Developmental
Gene Silencing
Homeodomain Proteins - genetics
Male
Meiosis
Mitosis
polycomb group proteins
Polycomb Repressive Complex 1
Regulatory Sequences, Nucleic Acid
Research Papers
Transcription Factors
X Chromosome
Title Inheritance of Polycomb-dependent chromosomal interactions in Drosophila
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