A histone methylation network regulates transgenerational epigenetic memory in C. elegans
A histone methylation network regulates transgenerational epigenetic memory in C. elegans
How epigenetic information is transmitted from generation to generation remains largely unknown. Deletion of the C. elegans histone H3 lysine 4 dimethyl (H3K4me2) demethylase spr-5 leads to inherited accumulation of the euchromatic H3K4me2 mark and progressive decline in fertility. Here, we identified multiple chromatin-modifying factors, including H3K4me1/me2 and H3K9me3 methyltransferases, an H3K9me3 demethylase, and an H3K9me reader, which either suppress or accelerate the progressive transgenerational phenotypes of spr-5 mutant worms. Our findings uncover a network of chromatin regulators that control the transgenerational flow of epigenetic information and suggest that the balance between euchromatic H3K4 and heterochromatic H3K9 methylation regulates transgenerational effects on fertility.
113-126
Greer, Eric L.
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Beese-Sims, Sara E.
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Brookes, Emily
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Spadafora, Ruggero
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Zhu, Yun
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Rothbart, Scott B.
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Aristizábal-Corrales, David
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Chen, Shuzhen
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Badeaux, Aimee I.
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Jin, Qiuye
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Wang, Wei
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Strahl, Brian D.
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Colaiácovo, Monica P.
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Shi, Yang
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10 April 2014
Greer, Eric L.
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Beese-Sims, Sara E.
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Brookes, Emily
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Spadafora, Ruggero
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Zhu, Yun
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Rothbart, Scott B.
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Aristizábal-Corrales, David
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Chen, Shuzhen
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Badeaux, Aimee I.
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Jin, Qiuye
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Wang, Wei
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Strahl, Brian D.
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Colaiácovo, Monica P.
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Shi, Yang
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Greer, Eric L., Beese-Sims, Sara E., Brookes, Emily, Spadafora, Ruggero, Zhu, Yun, Rothbart, Scott B., Aristizábal-Corrales, David, Chen, Shuzhen, Badeaux, Aimee I., Jin, Qiuye, Wang, Wei, Strahl, Brian D., Colaiácovo, Monica P. and Shi, Yang
(2014)
A histone methylation network regulates transgenerational epigenetic memory in C. elegans.
Cell Reports, 7 (1), .
(doi:10.1016/j.celrep.2014.02.044).
Abstract
How epigenetic information is transmitted from generation to generation remains largely unknown. Deletion of the C. elegans histone H3 lysine 4 dimethyl (H3K4me2) demethylase spr-5 leads to inherited accumulation of the euchromatic H3K4me2 mark and progressive decline in fertility. Here, we identified multiple chromatin-modifying factors, including H3K4me1/me2 and H3K9me3 methyltransferases, an H3K9me3 demethylase, and an H3K9me reader, which either suppress or accelerate the progressive transgenerational phenotypes of spr-5 mutant worms. Our findings uncover a network of chromatin regulators that control the transgenerational flow of epigenetic information and suggest that the balance between euchromatic H3K4 and heterochromatic H3K9 methylation regulates transgenerational effects on fertility.
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Published date: 10 April 2014
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Local EPrints ID: 472101
URI: http://eprints.soton.ac.uk/id/eprint/472101
ISSN: 2211-1247
PURE UUID: 30956bc3-2699-4fc2-a940-b689e81f84bb
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Date deposited: 25 Nov 2022 17:42
Last modified: 12 Nov 2024 03:10
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Contributors
Author:
Eric L. Greer
Author:
Sara E. Beese-Sims
Author:
Emily Brookes
Author:
Ruggero Spadafora
Author:
Yun Zhu
Author:
Scott B. Rothbart
Author:
David Aristizábal-Corrales
Author:
Shuzhen Chen
Author:
Aimee I. Badeaux
Author:
Qiuye Jin
Author:
Wei Wang
Author:
Brian D. Strahl
Author:
Monica P. Colaiácovo
Author:
Yang Shi
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