Cargando…
Transposable elements employ distinct integration strategies with respect to transcriptional landscapes in eukaryotic genomes
Transposable elements (TEs) are ubiquitous DNA segments capable of moving from one site to another within host genomes. The extant distributions of TEs in eukaryotic genomes have been shaped by both bona fide TE integration preferences in eukaryotic genomes and by selection following integration. He...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337890/ https://www.ncbi.nlm.nih.gov/pubmed/32442316 http://dx.doi.org/10.1093/nar/gkaa370 |
_version_ | 1783554574834991104 |
---|---|
author | Zhang, Xinyan Zhao, Meixia McCarty, Donald R Lisch, Damon |
author_facet | Zhang, Xinyan Zhao, Meixia McCarty, Donald R Lisch, Damon |
author_sort | Zhang, Xinyan |
collection | PubMed |
description | Transposable elements (TEs) are ubiquitous DNA segments capable of moving from one site to another within host genomes. The extant distributions of TEs in eukaryotic genomes have been shaped by both bona fide TE integration preferences in eukaryotic genomes and by selection following integration. Here, we compare TE target site distribution in host genomes using multiple de novo transposon insertion datasets in both plants and animals and compare them in the context of genome-wide transcriptional landscapes. We showcase two distinct types of transcription-associated TE targeting strategies that suggest a process of convergent evolution among eukaryotic TE families. The integration of two precision-targeting elements are specifically associated with initiation of RNA Polymerase II transcription of highly expressed genes, suggesting the existence of novel mechanisms of precision TE targeting in addition to passive targeting of open chromatin. We also highlight two features that can facilitate TE survival and rapid proliferation: tissue-specific transposition and minimization of negative impacts on nearby gene function due to precision targeting. |
format | Online Article Text |
id | pubmed-7337890 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-73378902020-07-13 Transposable elements employ distinct integration strategies with respect to transcriptional landscapes in eukaryotic genomes Zhang, Xinyan Zhao, Meixia McCarty, Donald R Lisch, Damon Nucleic Acids Res Genomics Transposable elements (TEs) are ubiquitous DNA segments capable of moving from one site to another within host genomes. The extant distributions of TEs in eukaryotic genomes have been shaped by both bona fide TE integration preferences in eukaryotic genomes and by selection following integration. Here, we compare TE target site distribution in host genomes using multiple de novo transposon insertion datasets in both plants and animals and compare them in the context of genome-wide transcriptional landscapes. We showcase two distinct types of transcription-associated TE targeting strategies that suggest a process of convergent evolution among eukaryotic TE families. The integration of two precision-targeting elements are specifically associated with initiation of RNA Polymerase II transcription of highly expressed genes, suggesting the existence of novel mechanisms of precision TE targeting in addition to passive targeting of open chromatin. We also highlight two features that can facilitate TE survival and rapid proliferation: tissue-specific transposition and minimization of negative impacts on nearby gene function due to precision targeting. Oxford University Press 2020-07-09 2020-05-22 /pmc/articles/PMC7337890/ /pubmed/32442316 http://dx.doi.org/10.1093/nar/gkaa370 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Genomics Zhang, Xinyan Zhao, Meixia McCarty, Donald R Lisch, Damon Transposable elements employ distinct integration strategies with respect to transcriptional landscapes in eukaryotic genomes |
title | Transposable elements employ distinct integration strategies with respect to transcriptional landscapes in eukaryotic genomes |
title_full | Transposable elements employ distinct integration strategies with respect to transcriptional landscapes in eukaryotic genomes |
title_fullStr | Transposable elements employ distinct integration strategies with respect to transcriptional landscapes in eukaryotic genomes |
title_full_unstemmed | Transposable elements employ distinct integration strategies with respect to transcriptional landscapes in eukaryotic genomes |
title_short | Transposable elements employ distinct integration strategies with respect to transcriptional landscapes in eukaryotic genomes |
title_sort | transposable elements employ distinct integration strategies with respect to transcriptional landscapes in eukaryotic genomes |
topic | Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337890/ https://www.ncbi.nlm.nih.gov/pubmed/32442316 http://dx.doi.org/10.1093/nar/gkaa370 |
work_keys_str_mv | AT zhangxinyan transposableelementsemploydistinctintegrationstrategieswithrespecttotranscriptionallandscapesineukaryoticgenomes AT zhaomeixia transposableelementsemploydistinctintegrationstrategieswithrespecttotranscriptionallandscapesineukaryoticgenomes AT mccartydonaldr transposableelementsemploydistinctintegrationstrategieswithrespecttotranscriptionallandscapesineukaryoticgenomes AT lischdamon transposableelementsemploydistinctintegrationstrategieswithrespecttotranscriptionallandscapesineukaryoticgenomes |