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Evolutionary rewiring of the wheat transcriptional regulatory network by lineage-specific transposable elements

More than 80% of the wheat genome consists of transposable elements (TEs), which act as major drivers of wheat genome evolution. However, their contributions to the regulatory evolution of wheat adaptations remain largely unclear. Here, we created genome-binding maps for 53 transcription factors (TF...

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Autores principales: Zhang, Yuyun, Li, Zijuan, Zhang, Yu'e, Lin, Kande, Peng, Yuan, Ye, Luhuan, Zhuang, Yili, Wang, Meiyue, Xie, Yilin, Guo, Jingyu, Teng, Wan, Tong, Yiping, Zhang, Wenli, Xue, Yongbiao, Lang, Zhaobo, Zhang, Yijing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647832/
https://www.ncbi.nlm.nih.gov/pubmed/34503979
http://dx.doi.org/10.1101/gr.275658.121
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author Zhang, Yuyun
Li, Zijuan
Zhang, Yu'e
Lin, Kande
Peng, Yuan
Ye, Luhuan
Zhuang, Yili
Wang, Meiyue
Xie, Yilin
Guo, Jingyu
Teng, Wan
Tong, Yiping
Zhang, Wenli
Xue, Yongbiao
Lang, Zhaobo
Zhang, Yijing
author_facet Zhang, Yuyun
Li, Zijuan
Zhang, Yu'e
Lin, Kande
Peng, Yuan
Ye, Luhuan
Zhuang, Yili
Wang, Meiyue
Xie, Yilin
Guo, Jingyu
Teng, Wan
Tong, Yiping
Zhang, Wenli
Xue, Yongbiao
Lang, Zhaobo
Zhang, Yijing
author_sort Zhang, Yuyun
collection PubMed
description More than 80% of the wheat genome consists of transposable elements (TEs), which act as major drivers of wheat genome evolution. However, their contributions to the regulatory evolution of wheat adaptations remain largely unclear. Here, we created genome-binding maps for 53 transcription factors (TFs) underlying environmental responses by leveraging DAP-seq in Triticum urartu, together with epigenomic profiles. Most TF binding sites (TFBSs) located distally from genes are embedded in TEs, whose functional relevance is supported by purifying selection and active epigenomic features. About 24% of the non-TE TFBSs share significantly high sequence similarity with TE-embedded TFBSs. These non-TE TFBSs have almost no homologous sequences in non-Triticeae species and are potentially derived from Triticeae-specific TEs. The expansion of TE-derived TFBS linked to wheat-specific gene responses, suggesting TEs are an important driving force for regulatory innovations. Altogether, TEs have been significantly and continuously shaping regulatory networks related to wheat genome evolution and adaptation.
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spelling pubmed-86478322022-06-01 Evolutionary rewiring of the wheat transcriptional regulatory network by lineage-specific transposable elements Zhang, Yuyun Li, Zijuan Zhang, Yu'e Lin, Kande Peng, Yuan Ye, Luhuan Zhuang, Yili Wang, Meiyue Xie, Yilin Guo, Jingyu Teng, Wan Tong, Yiping Zhang, Wenli Xue, Yongbiao Lang, Zhaobo Zhang, Yijing Genome Res Research More than 80% of the wheat genome consists of transposable elements (TEs), which act as major drivers of wheat genome evolution. However, their contributions to the regulatory evolution of wheat adaptations remain largely unclear. Here, we created genome-binding maps for 53 transcription factors (TFs) underlying environmental responses by leveraging DAP-seq in Triticum urartu, together with epigenomic profiles. Most TF binding sites (TFBSs) located distally from genes are embedded in TEs, whose functional relevance is supported by purifying selection and active epigenomic features. About 24% of the non-TE TFBSs share significantly high sequence similarity with TE-embedded TFBSs. These non-TE TFBSs have almost no homologous sequences in non-Triticeae species and are potentially derived from Triticeae-specific TEs. The expansion of TE-derived TFBS linked to wheat-specific gene responses, suggesting TEs are an important driving force for regulatory innovations. Altogether, TEs have been significantly and continuously shaping regulatory networks related to wheat genome evolution and adaptation. Cold Spring Harbor Laboratory Press 2021-12 /pmc/articles/PMC8647832/ /pubmed/34503979 http://dx.doi.org/10.1101/gr.275658.121 Text en © 2021 Zhang et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see https://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Research
Zhang, Yuyun
Li, Zijuan
Zhang, Yu'e
Lin, Kande
Peng, Yuan
Ye, Luhuan
Zhuang, Yili
Wang, Meiyue
Xie, Yilin
Guo, Jingyu
Teng, Wan
Tong, Yiping
Zhang, Wenli
Xue, Yongbiao
Lang, Zhaobo
Zhang, Yijing
Evolutionary rewiring of the wheat transcriptional regulatory network by lineage-specific transposable elements
title Evolutionary rewiring of the wheat transcriptional regulatory network by lineage-specific transposable elements
title_full Evolutionary rewiring of the wheat transcriptional regulatory network by lineage-specific transposable elements
title_fullStr Evolutionary rewiring of the wheat transcriptional regulatory network by lineage-specific transposable elements
title_full_unstemmed Evolutionary rewiring of the wheat transcriptional regulatory network by lineage-specific transposable elements
title_short Evolutionary rewiring of the wheat transcriptional regulatory network by lineage-specific transposable elements
title_sort evolutionary rewiring of the wheat transcriptional regulatory network by lineage-specific transposable elements
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647832/
https://www.ncbi.nlm.nih.gov/pubmed/34503979
http://dx.doi.org/10.1101/gr.275658.121
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