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Ovaries absent links dLsd1 to HP1a for local H3K4 demethylation required for heterochromatic gene silencing
Heterochromatin Protein 1 (HP1) is a conserved chromosomal protein in eukaryotic cells that has a major role in directing heterochromatin formation, a process that requires co-transcriptional gene silencing mediated by small RNAs and their associated argonaute proteins. Heterochromatin formation req...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335052/ https://www.ncbi.nlm.nih.gov/pubmed/30648969 http://dx.doi.org/10.7554/eLife.40806 |
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author | Yang, Fu Quan, Zhenghui Huang, Huanwei He, Minghui Liu, Xicheng Cai, Tao Xi, Rongwen |
author_facet | Yang, Fu Quan, Zhenghui Huang, Huanwei He, Minghui Liu, Xicheng Cai, Tao Xi, Rongwen |
author_sort | Yang, Fu |
collection | PubMed |
description | Heterochromatin Protein 1 (HP1) is a conserved chromosomal protein in eukaryotic cells that has a major role in directing heterochromatin formation, a process that requires co-transcriptional gene silencing mediated by small RNAs and their associated argonaute proteins. Heterochromatin formation requires erasing the active epigenetic mark, such as H3K4me2, but the molecular link between HP1 and H3K4 demethylation remains unclear. In a fertility screen in female Drosophila, we identified ovaries absent (ova), which functions in the stem cell niche, downstream of Piwi, to support germline stem cell differentiation. Moreover, ova acts as a suppressor of position effect variegation, and is required for silencing telomeric transposons in the germline. Biochemically, Ova acts to link the H3K4 demethylase dLsd1 to HP1a for local histone modifications. Therefore, our study provides a molecular connection between HP1a and local H3K4 demethylation during HP1a-mediated gene silencing that is required for ovary development, transposon silencing, and heterochromatin formation. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter). |
format | Online Article Text |
id | pubmed-6335052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63350522019-01-24 Ovaries absent links dLsd1 to HP1a for local H3K4 demethylation required for heterochromatic gene silencing Yang, Fu Quan, Zhenghui Huang, Huanwei He, Minghui Liu, Xicheng Cai, Tao Xi, Rongwen eLife Stem Cells and Regenerative Medicine Heterochromatin Protein 1 (HP1) is a conserved chromosomal protein in eukaryotic cells that has a major role in directing heterochromatin formation, a process that requires co-transcriptional gene silencing mediated by small RNAs and their associated argonaute proteins. Heterochromatin formation requires erasing the active epigenetic mark, such as H3K4me2, but the molecular link between HP1 and H3K4 demethylation remains unclear. In a fertility screen in female Drosophila, we identified ovaries absent (ova), which functions in the stem cell niche, downstream of Piwi, to support germline stem cell differentiation. Moreover, ova acts as a suppressor of position effect variegation, and is required for silencing telomeric transposons in the germline. Biochemically, Ova acts to link the H3K4 demethylase dLsd1 to HP1a for local histone modifications. Therefore, our study provides a molecular connection between HP1a and local H3K4 demethylation during HP1a-mediated gene silencing that is required for ovary development, transposon silencing, and heterochromatin formation. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter). eLife Sciences Publications, Ltd 2019-01-16 /pmc/articles/PMC6335052/ /pubmed/30648969 http://dx.doi.org/10.7554/eLife.40806 Text en © 2019, Yang et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Stem Cells and Regenerative Medicine Yang, Fu Quan, Zhenghui Huang, Huanwei He, Minghui Liu, Xicheng Cai, Tao Xi, Rongwen Ovaries absent links dLsd1 to HP1a for local H3K4 demethylation required for heterochromatic gene silencing |
title | Ovaries absent links dLsd1 to HP1a for local H3K4 demethylation required for heterochromatic gene silencing |
title_full | Ovaries absent links dLsd1 to HP1a for local H3K4 demethylation required for heterochromatic gene silencing |
title_fullStr | Ovaries absent links dLsd1 to HP1a for local H3K4 demethylation required for heterochromatic gene silencing |
title_full_unstemmed | Ovaries absent links dLsd1 to HP1a for local H3K4 demethylation required for heterochromatic gene silencing |
title_short | Ovaries absent links dLsd1 to HP1a for local H3K4 demethylation required for heterochromatic gene silencing |
title_sort | ovaries absent links dlsd1 to hp1a for local h3k4 demethylation required for heterochromatic gene silencing |
topic | Stem Cells and Regenerative Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335052/ https://www.ncbi.nlm.nih.gov/pubmed/30648969 http://dx.doi.org/10.7554/eLife.40806 |
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