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 in | Genes & development Vol. 17; no. 19; pp. 2406 - 2420 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Cold Spring Harbor Laboratory Press
01.10.2003
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Subjects | |
Online Access | Get full text |
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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 |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/14522946$$D View this record in MEDLINE/PubMed |
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Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 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 |
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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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