The modular mechanism of chromocenter formation in Drosophila

A central principle underlying the ubiquity and abundance of pericentromeric satellite DNA repeats in eukaryotes has remained poorly understood. Previously we proposed that the interchromosomal clustering of satellite DNAs into nuclear structures known as chromocenters ensures encapsulation of all c...

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Main Authors: Madhav Jagannathan, Ryan Cummings, Yukiko M Yamashita
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2019-02-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/43938
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spelling doaj-468732f2f08a48e2afe1ef543ce449ec2021-05-05T17:24:11ZengeLife Sciences Publications LtdeLife2050-084X2019-02-01810.7554/eLife.43938The modular mechanism of chromocenter formation in DrosophilaMadhav Jagannathan0https://orcid.org/0000-0003-3428-6812Ryan Cummings1https://orcid.org/0000-0003-0540-9174Yukiko M Yamashita2https://orcid.org/0000-0001-5541-0216Life Sciences Institute, University of Michigan, Ann Arbor, United StatesHoward Hughes Medical Institute, University of Michigan, Ann Arbor, United StatesHoward Hughes Medical Institute, University of Michigan, Ann Arbor, United States; Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, United StatesA central principle underlying the ubiquity and abundance of pericentromeric satellite DNA repeats in eukaryotes has remained poorly understood. Previously we proposed that the interchromosomal clustering of satellite DNAs into nuclear structures known as chromocenters ensures encapsulation of all chromosomes into a single nucleus (Jagannathan et al., 2018). Chromocenter disruption led to micronuclei formation, resulting in cell death. Here we show that chromocenter formation is mediated by a ‘modular’ network, where associations between two sequence-specific satellite DNA-binding proteins, D1 and Prod, bound to their cognate satellite DNAs, bring the full complement of chromosomes into the chromocenter. D1 prod double mutants die during embryogenesis, exhibiting enhanced phenotypes associated with chromocenter disruption, revealing the universal importance of satellite DNAs and chromocenters. Taken together, we propose that associations between chromocenter modules, consisting of satellite DNA binding proteins and their cognate satellite DNA, package the Drosophila genome within a single nucleus.https://elifesciences.org/articles/43938chromocentersatellite DNAmicronuclei
collection DOAJ
language English
format Article
sources DOAJ
author Madhav Jagannathan
Ryan Cummings
Yukiko M Yamashita
spellingShingle Madhav Jagannathan
Ryan Cummings
Yukiko M Yamashita
The modular mechanism of chromocenter formation in Drosophila
eLife
chromocenter
satellite DNA
micronuclei
author_facet Madhav Jagannathan
Ryan Cummings
Yukiko M Yamashita
author_sort Madhav Jagannathan
title The modular mechanism of chromocenter formation in Drosophila
title_short The modular mechanism of chromocenter formation in Drosophila
title_full The modular mechanism of chromocenter formation in Drosophila
title_fullStr The modular mechanism of chromocenter formation in Drosophila
title_full_unstemmed The modular mechanism of chromocenter formation in Drosophila
title_sort modular mechanism of chromocenter formation in drosophila
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2019-02-01
description A central principle underlying the ubiquity and abundance of pericentromeric satellite DNA repeats in eukaryotes has remained poorly understood. Previously we proposed that the interchromosomal clustering of satellite DNAs into nuclear structures known as chromocenters ensures encapsulation of all chromosomes into a single nucleus (Jagannathan et al., 2018). Chromocenter disruption led to micronuclei formation, resulting in cell death. Here we show that chromocenter formation is mediated by a ‘modular’ network, where associations between two sequence-specific satellite DNA-binding proteins, D1 and Prod, bound to their cognate satellite DNAs, bring the full complement of chromosomes into the chromocenter. D1 prod double mutants die during embryogenesis, exhibiting enhanced phenotypes associated with chromocenter disruption, revealing the universal importance of satellite DNAs and chromocenters. Taken together, we propose that associations between chromocenter modules, consisting of satellite DNA binding proteins and their cognate satellite DNA, package the Drosophila genome within a single nucleus.
topic chromocenter
satellite DNA
micronuclei
url https://elifesciences.org/articles/43938
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