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A satellite repeat-derived piRNA controls embryonic development of Aedes
Tandem repeat elements such as the diverse class of satellite repeats occupy large parts of eukaryotic chromosomes, mostly at (peri)centromeric and (sub)telomeric regions(1). Some elements, however, are located in euchromatic regions throughout the genome and were hypothesized to regulate gene expre...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145458/ https://www.ncbi.nlm.nih.gov/pubmed/32269344 http://dx.doi.org/10.1038/s41586-020-2159-2 |
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author | Halbach, Rebecca Miesen, Pascal Joosten, Joep Taşköprü, Ezgi Rondeel, Inge Pennings, Bas Vogels, Chantal B.F. Merkling, Sarah H. Koenraadt, Constantianus J. Lambrechts, Louis van Rij, Ronald P. |
author_facet | Halbach, Rebecca Miesen, Pascal Joosten, Joep Taşköprü, Ezgi Rondeel, Inge Pennings, Bas Vogels, Chantal B.F. Merkling, Sarah H. Koenraadt, Constantianus J. Lambrechts, Louis van Rij, Ronald P. |
author_sort | Halbach, Rebecca |
collection | PubMed |
description | Tandem repeat elements such as the diverse class of satellite repeats occupy large parts of eukaryotic chromosomes, mostly at (peri)centromeric and (sub)telomeric regions(1). Some elements, however, are located in euchromatic regions throughout the genome and were hypothesized to regulate gene expression in cis by modulating local chromatin structure, or in trans via repeat-derived transcripts(2–4). Here we show that a satellite repeat in the mosquito Aedes aegypti promotes sequence-specific gene silencing via the expression of two PIWI-interacting RNAs (piRNAs). Whereas satellite repeats and piRNA sequences generally evolve extremely fast(5–7), this locus was conserved for approximately 200 million years, suggesting a central function in mosquito biology. piRNA production commenced shortly after egg-laying, and inactivation of the more abundant of the piRNAs resulted in failure to degrade maternally provided transcripts and developmental arrest. Our results reveal a novel mechanism by which satellite repeats regulate global gene expression in trans via piRNA-mediated gene silencing that is essential for embryonic development. |
format | Online Article Text |
id | pubmed-7145458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-71454582020-10-01 A satellite repeat-derived piRNA controls embryonic development of Aedes Halbach, Rebecca Miesen, Pascal Joosten, Joep Taşköprü, Ezgi Rondeel, Inge Pennings, Bas Vogels, Chantal B.F. Merkling, Sarah H. Koenraadt, Constantianus J. Lambrechts, Louis van Rij, Ronald P. Nature Article Tandem repeat elements such as the diverse class of satellite repeats occupy large parts of eukaryotic chromosomes, mostly at (peri)centromeric and (sub)telomeric regions(1). Some elements, however, are located in euchromatic regions throughout the genome and were hypothesized to regulate gene expression in cis by modulating local chromatin structure, or in trans via repeat-derived transcripts(2–4). Here we show that a satellite repeat in the mosquito Aedes aegypti promotes sequence-specific gene silencing via the expression of two PIWI-interacting RNAs (piRNAs). Whereas satellite repeats and piRNA sequences generally evolve extremely fast(5–7), this locus was conserved for approximately 200 million years, suggesting a central function in mosquito biology. piRNA production commenced shortly after egg-laying, and inactivation of the more abundant of the piRNAs resulted in failure to degrade maternally provided transcripts and developmental arrest. Our results reveal a novel mechanism by which satellite repeats regulate global gene expression in trans via piRNA-mediated gene silencing that is essential for embryonic development. 2020-04-01 2020-04-09 /pmc/articles/PMC7145458/ /pubmed/32269344 http://dx.doi.org/10.1038/s41586-020-2159-2 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Halbach, Rebecca Miesen, Pascal Joosten, Joep Taşköprü, Ezgi Rondeel, Inge Pennings, Bas Vogels, Chantal B.F. Merkling, Sarah H. Koenraadt, Constantianus J. Lambrechts, Louis van Rij, Ronald P. A satellite repeat-derived piRNA controls embryonic development of Aedes |
title | A satellite repeat-derived piRNA controls embryonic development of Aedes |
title_full | A satellite repeat-derived piRNA controls embryonic development of Aedes |
title_fullStr | A satellite repeat-derived piRNA controls embryonic development of Aedes |
title_full_unstemmed | A satellite repeat-derived piRNA controls embryonic development of Aedes |
title_short | A satellite repeat-derived piRNA controls embryonic development of Aedes |
title_sort | satellite repeat-derived pirna controls embryonic development of aedes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145458/ https://www.ncbi.nlm.nih.gov/pubmed/32269344 http://dx.doi.org/10.1038/s41586-020-2159-2 |
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