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The KRAB-zinc-finger protein ZFP708 mediates epigenetic repression at RMER19B retrotransposons

Global epigenetic reprogramming is vital to purge germ cell-specific epigenetic features to establish the totipotent state of the embryo. This process transpires to be carefully regulated and is not an undirected, radical erasure of parental epigenomes. The TRIM28 complex has been shown to be crucia...

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Autores principales: Seah, Michelle K. Y., Wang, Yaju, Goy, Pierre-Alexis, Loh, Hui Mun, Peh, Wen Jun, Low, Diana H. P., Han, Brenda Y., Wong, Esther, Leong, Ei Leen, Wolf, Gernot, Mzoughi, Slim, Wollmann, Heike, Macfarlan, Todd S., Guccione, Ernesto, Messerschmidt, Daniel M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6803371/
https://www.ncbi.nlm.nih.gov/pubmed/30846446
http://dx.doi.org/10.1242/dev.170266
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author Seah, Michelle K. Y.
Wang, Yaju
Goy, Pierre-Alexis
Loh, Hui Mun
Peh, Wen Jun
Low, Diana H. P.
Han, Brenda Y.
Wong, Esther
Leong, Ei Leen
Wolf, Gernot
Mzoughi, Slim
Wollmann, Heike
Macfarlan, Todd S.
Guccione, Ernesto
Messerschmidt, Daniel M.
author_facet Seah, Michelle K. Y.
Wang, Yaju
Goy, Pierre-Alexis
Loh, Hui Mun
Peh, Wen Jun
Low, Diana H. P.
Han, Brenda Y.
Wong, Esther
Leong, Ei Leen
Wolf, Gernot
Mzoughi, Slim
Wollmann, Heike
Macfarlan, Todd S.
Guccione, Ernesto
Messerschmidt, Daniel M.
author_sort Seah, Michelle K. Y.
collection PubMed
description Global epigenetic reprogramming is vital to purge germ cell-specific epigenetic features to establish the totipotent state of the embryo. This process transpires to be carefully regulated and is not an undirected, radical erasure of parental epigenomes. The TRIM28 complex has been shown to be crucial in embryonic epigenetic reprogramming by regionally opposing DNA demethylation to preserve vital parental information to be inherited from germline to soma. Yet the DNA-binding factors guiding this complex to specific targets are largely unknown. Here, we uncover and characterize a novel, maternally expressed, TRIM28-interacting KRAB zinc-finger protein: ZFP708. It recruits the repressive TRIM28 complex to RMER19B retrotransposons to evoke regional heterochromatin formation. ZFP708 binding to these hitherto unknown TRIM28 targets is DNA methylation and H3K9me3 independent. ZFP708 mutant mice are viable and fertile, yet embryos fail to inherit and maintain DNA methylation at ZFP708 target sites. This can result in activation of RMER19B-adjacent genes, while ectopic expression of ZFP708 results in transcriptional repression. Finally, we describe the evolutionary conservation of ZFP708 in mice and rats, which is linked to the conserved presence of the targeted RMER19B retrotransposons in these species.
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spelling pubmed-68033712019-10-30 The KRAB-zinc-finger protein ZFP708 mediates epigenetic repression at RMER19B retrotransposons Seah, Michelle K. Y. Wang, Yaju Goy, Pierre-Alexis Loh, Hui Mun Peh, Wen Jun Low, Diana H. P. Han, Brenda Y. Wong, Esther Leong, Ei Leen Wolf, Gernot Mzoughi, Slim Wollmann, Heike Macfarlan, Todd S. Guccione, Ernesto Messerschmidt, Daniel M. Development Research Article Global epigenetic reprogramming is vital to purge germ cell-specific epigenetic features to establish the totipotent state of the embryo. This process transpires to be carefully regulated and is not an undirected, radical erasure of parental epigenomes. The TRIM28 complex has been shown to be crucial in embryonic epigenetic reprogramming by regionally opposing DNA demethylation to preserve vital parental information to be inherited from germline to soma. Yet the DNA-binding factors guiding this complex to specific targets are largely unknown. Here, we uncover and characterize a novel, maternally expressed, TRIM28-interacting KRAB zinc-finger protein: ZFP708. It recruits the repressive TRIM28 complex to RMER19B retrotransposons to evoke regional heterochromatin formation. ZFP708 binding to these hitherto unknown TRIM28 targets is DNA methylation and H3K9me3 independent. ZFP708 mutant mice are viable and fertile, yet embryos fail to inherit and maintain DNA methylation at ZFP708 target sites. This can result in activation of RMER19B-adjacent genes, while ectopic expression of ZFP708 results in transcriptional repression. Finally, we describe the evolutionary conservation of ZFP708 in mice and rats, which is linked to the conserved presence of the targeted RMER19B retrotransposons in these species. The Company of Biologists Ltd 2019-10-01 2019-07-10 /pmc/articles/PMC6803371/ /pubmed/30846446 http://dx.doi.org/10.1242/dev.170266 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Seah, Michelle K. Y.
Wang, Yaju
Goy, Pierre-Alexis
Loh, Hui Mun
Peh, Wen Jun
Low, Diana H. P.
Han, Brenda Y.
Wong, Esther
Leong, Ei Leen
Wolf, Gernot
Mzoughi, Slim
Wollmann, Heike
Macfarlan, Todd S.
Guccione, Ernesto
Messerschmidt, Daniel M.
The KRAB-zinc-finger protein ZFP708 mediates epigenetic repression at RMER19B retrotransposons
title The KRAB-zinc-finger protein ZFP708 mediates epigenetic repression at RMER19B retrotransposons
title_full The KRAB-zinc-finger protein ZFP708 mediates epigenetic repression at RMER19B retrotransposons
title_fullStr The KRAB-zinc-finger protein ZFP708 mediates epigenetic repression at RMER19B retrotransposons
title_full_unstemmed The KRAB-zinc-finger protein ZFP708 mediates epigenetic repression at RMER19B retrotransposons
title_short The KRAB-zinc-finger protein ZFP708 mediates epigenetic repression at RMER19B retrotransposons
title_sort krab-zinc-finger protein zfp708 mediates epigenetic repression at rmer19b retrotransposons
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6803371/
https://www.ncbi.nlm.nih.gov/pubmed/30846446
http://dx.doi.org/10.1242/dev.170266
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