A novel anti-RdDM element that defends cis-regulatory element against ncRNA-dependent, siRNA-driven, and methylation-imposed transcriptional silencing in plants [ARE BSseq]

Cis-regulatory elements (CREs) dictate spatiotemporal expression and tissue specificity of proximal genes. However, when in a transgenic state, many of them become highly vulnerable to RNA-Directed DNA Methylation (RdDM) that is often transcriptionally deleterious and biologically detrimental. This transgene-specific RdDM vulnerability suggests the existence of anti-RdDM elements (AREs) to defend CREs against de novo methylation in vivo. In this work, we identify such an ARE at the Arabidopsis AGAMOUS (AG) locus, which includes a physically separated enhancer and promoter, both of which are highly vulnerable to transgene silencing. We demonstrate that this ARE effectively represses RdDM activity at its cognate and heterologous CREs via the inhibition of transcription and processing of potent non-coding RNAs (ncRNAs), which act as substrates for the biogenesis of 24-nt small interfering RNAs (siRNAs) that guide RdDM. Furthermore, we establish that the ARE exploits hypermethylation in a 108-bp internal region (referred to as M1) as a regulatory signal to recruit methyl reader SU(VAR)3-9 homolog 1 (SUVH1), as well as Harbinger transposon-derived protein 2 (HDP2) associated with HDP1, to carry out ARE-imposed transcriptional and post-transcriptional repression, with the former mediating the repression of ncRNA transcription and the latter repressing both ncRNA transcription and processing. We also show that M1 methylation is indispensable for the repression of methylation in an adjacent, methylation-vulnerable 737-bp region (dubbed M2) to safeguard the ARE’s functional integrity. Taken together, the present study uncovers a novel anti-RdDM element that defends CREs against ncRNA-dependent, siRNA-driven, and methylation-imposed epigenetic interference to safeguard their regulatory integrity. Overall design: Comparison of DNA methylation profile among different lines

Saved in:
Bibliographic Details
Main Author: Zongrang Liu, Appalachian Fruit Research Station, USDA-ARS (18797563)
Format: Dataset biblioteca
Published: 2023
Subjects:Genetics, Arabidopsis thaliana, eEukaryotes,
Online Access:https://figshare.com/articles/dataset/A_novel_anti-RdDM_element_that_defends_cis-regulatory_element_against_ncRNA-dependent_siRNA-driven_and_methylation-imposed_transcriptional_silencing_in_plants_ARE_BSseq_/25091105
Tags: Add Tag
No Tags, Be the first to tag this record!
id dat-usda-us-article25091105
record_format figshare
spelling dat-usda-us-article250911052023-03-29T00:00:00Z A novel anti-RdDM element that defends cis-regulatory element against ncRNA-dependent, siRNA-driven, and methylation-imposed transcriptional silencing in plants [ARE BSseq] Zongrang Liu, Appalachian Fruit Research Station, USDA-ARS (18797563) Genetics Arabidopsis thaliana eEukaryotes Cis-regulatory elements (CREs) dictate spatiotemporal expression and tissue specificity of proximal genes. However, when in a transgenic state, many of them become highly vulnerable to RNA-Directed DNA Methylation (RdDM) that is often transcriptionally deleterious and biologically detrimental. This transgene-specific RdDM vulnerability suggests the existence of anti-RdDM elements (AREs) to defend CREs against de novo methylation in vivo. In this work, we identify such an ARE at the Arabidopsis AGAMOUS (AG) locus, which includes a physically separated enhancer and promoter, both of which are highly vulnerable to transgene silencing. We demonstrate that this ARE effectively represses RdDM activity at its cognate and heterologous CREs via the inhibition of transcription and processing of potent non-coding RNAs (ncRNAs), which act as substrates for the biogenesis of 24-nt small interfering RNAs (siRNAs) that guide RdDM. Furthermore, we establish that the ARE exploits hypermethylation in a 108-bp internal region (referred to as M1) as a regulatory signal to recruit methyl reader SU(VAR)3-9 homolog 1 (SUVH1), as well as Harbinger transposon-derived protein 2 (HDP2) associated with HDP1, to carry out ARE-imposed transcriptional and post-transcriptional repression, with the former mediating the repression of ncRNA transcription and the latter repressing both ncRNA transcription and processing. We also show that M1 methylation is indispensable for the repression of methylation in an adjacent, methylation-vulnerable 737-bp region (dubbed M2) to safeguard the ARE’s functional integrity. Taken together, the present study uncovers a novel anti-RdDM element that defends CREs against ncRNA-dependent, siRNA-driven, and methylation-imposed epigenetic interference to safeguard their regulatory integrity. Overall design: Comparison of DNA methylation profile among different lines 2023-03-29T00:00:00Z Dataset Dataset 10113/AF25091105 https://figshare.com/articles/dataset/A_novel_anti-RdDM_element_that_defends_cis-regulatory_element_against_ncRNA-dependent_siRNA-driven_and_methylation-imposed_transcriptional_silencing_in_plants_ARE_BSseq_/25091105 Copyright Undetermined
institution USDA US
collection Figshare
country Estados Unidos
countrycode US
component Datos de investigación
access En linea
databasecode dat-usda-us
tag biblioteca
region America del Norte
libraryname National Agricultural Library of USDA
topic Genetics
Arabidopsis thaliana
eEukaryotes
spellingShingle Genetics
Arabidopsis thaliana
eEukaryotes
Zongrang Liu, Appalachian Fruit Research Station, USDA-ARS (18797563)
A novel anti-RdDM element that defends cis-regulatory element against ncRNA-dependent, siRNA-driven, and methylation-imposed transcriptional silencing in plants [ARE BSseq]
description Cis-regulatory elements (CREs) dictate spatiotemporal expression and tissue specificity of proximal genes. However, when in a transgenic state, many of them become highly vulnerable to RNA-Directed DNA Methylation (RdDM) that is often transcriptionally deleterious and biologically detrimental. This transgene-specific RdDM vulnerability suggests the existence of anti-RdDM elements (AREs) to defend CREs against de novo methylation in vivo. In this work, we identify such an ARE at the Arabidopsis AGAMOUS (AG) locus, which includes a physically separated enhancer and promoter, both of which are highly vulnerable to transgene silencing. We demonstrate that this ARE effectively represses RdDM activity at its cognate and heterologous CREs via the inhibition of transcription and processing of potent non-coding RNAs (ncRNAs), which act as substrates for the biogenesis of 24-nt small interfering RNAs (siRNAs) that guide RdDM. Furthermore, we establish that the ARE exploits hypermethylation in a 108-bp internal region (referred to as M1) as a regulatory signal to recruit methyl reader SU(VAR)3-9 homolog 1 (SUVH1), as well as Harbinger transposon-derived protein 2 (HDP2) associated with HDP1, to carry out ARE-imposed transcriptional and post-transcriptional repression, with the former mediating the repression of ncRNA transcription and the latter repressing both ncRNA transcription and processing. We also show that M1 methylation is indispensable for the repression of methylation in an adjacent, methylation-vulnerable 737-bp region (dubbed M2) to safeguard the ARE’s functional integrity. Taken together, the present study uncovers a novel anti-RdDM element that defends CREs against ncRNA-dependent, siRNA-driven, and methylation-imposed epigenetic interference to safeguard their regulatory integrity. Overall design: Comparison of DNA methylation profile among different lines
format Dataset
author Zongrang Liu, Appalachian Fruit Research Station, USDA-ARS (18797563)
author_facet Zongrang Liu, Appalachian Fruit Research Station, USDA-ARS (18797563)
author_sort Zongrang Liu, Appalachian Fruit Research Station, USDA-ARS (18797563)
title A novel anti-RdDM element that defends cis-regulatory element against ncRNA-dependent, siRNA-driven, and methylation-imposed transcriptional silencing in plants [ARE BSseq]
title_short A novel anti-RdDM element that defends cis-regulatory element against ncRNA-dependent, siRNA-driven, and methylation-imposed transcriptional silencing in plants [ARE BSseq]
title_full A novel anti-RdDM element that defends cis-regulatory element against ncRNA-dependent, siRNA-driven, and methylation-imposed transcriptional silencing in plants [ARE BSseq]
title_fullStr A novel anti-RdDM element that defends cis-regulatory element against ncRNA-dependent, siRNA-driven, and methylation-imposed transcriptional silencing in plants [ARE BSseq]
title_full_unstemmed A novel anti-RdDM element that defends cis-regulatory element against ncRNA-dependent, siRNA-driven, and methylation-imposed transcriptional silencing in plants [ARE BSseq]
title_sort novel anti-rddm element that defends cis-regulatory element against ncrna-dependent, sirna-driven, and methylation-imposed transcriptional silencing in plants [are bsseq]
publishDate 2023
url https://figshare.com/articles/dataset/A_novel_anti-RdDM_element_that_defends_cis-regulatory_element_against_ncRNA-dependent_siRNA-driven_and_methylation-imposed_transcriptional_silencing_in_plants_ARE_BSseq_/25091105
work_keys_str_mv AT zongrangliuappalachianfruitresearchstationusdaars18797563 anovelantirddmelementthatdefendscisregulatoryelementagainstncrnadependentsirnadrivenandmethylationimposedtranscriptionalsilencinginplantsarebsseq
AT zongrangliuappalachianfruitresearchstationusdaars18797563 novelantirddmelementthatdefendscisregulatoryelementagainstncrnadependentsirnadrivenandmethylationimposedtranscriptionalsilencinginplantsarebsseq
_version_ 1806232860445638656