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PNAS

Mobile small RNAs regulate genome-wide DNA methylation

Overview of attention for article published in Proceedings of the National Academy of Sciences of the United States of America, January 2016
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About this Attention Score

  • In the top 5% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (97th percentile)
  • Good Attention Score compared to outputs of the same age and source (76th percentile)

Mentioned by

news
6 news outlets
blogs
1 blog
twitter
53 X users
facebook
2 Facebook pages
wikipedia
1 Wikipedia page
googleplus
1 Google+ user
reddit
1 Redditor
video
1 YouTube creator

Citations

dimensions_citation
200 Dimensions

Readers on

mendeley
430 Mendeley
citeulike
1 CiteULike
Title
Mobile small RNAs regulate genome-wide DNA methylation
Published in
Proceedings of the National Academy of Sciences of the United States of America, January 2016
DOI 10.1073/pnas.1515072113
Pubmed ID
Authors

Mathew G Lewsey, Thomas J Hardcastle, Charles W Melnyk, Attila Molnar, Adrián Valli, Mark A Urich, Joseph R Nery, David C Baulcombe, Joseph R Ecker

Abstract

RNA silencing at the transcriptional and posttranscriptional levels regulates endogenous gene expression, controls invading transposable elements (TEs), and protects the cell against viruses. Key components of the mechanism are small RNAs (sRNAs) of 21-24 nt that guide the silencing machinery to their nucleic acid targets in a nucleotide sequence-specific manner. Transcriptional gene silencing is associated with 24-nt sRNAs and RNA-directed DNA methylation (RdDM) at cytosine residues in three DNA sequence contexts (CG, CHG, and CHH). We previously demonstrated that 24-nt sRNAs are mobile from shoot to root in Arabidopsis thaliana and confirmed that they mediate DNA methylation at three sites in recipient cells. In this study, we extend this finding by demonstrating that RdDM of thousands of loci in root tissues is dependent upon mobile sRNAs from the shoot and that mobile sRNA-dependent DNA methylation occurs predominantly in non-CG contexts. Mobile sRNA-dependent non-CG methylation is largely dependent on the DOMAINS REARRANGED METHYLTRANSFERASES 1/2 (DRM1/DRM2) RdDM pathway but is independent of the CHROMOMETHYLASE (CMT)2/3 DNA methyltransferases. Specific superfamilies of TEs, including those typically found in gene-rich euchromatic regions, lose DNA methylation in a mutant lacking 22- to 24-nt sRNAs (dicer-like 2, 3, 4 triple mutant). Transcriptome analyses identified a small number of genes whose expression in roots is associated with mobile sRNAs and connected to DNA methylation directly or indirectly. Finally, we demonstrate that sRNAs from shoots of one accession move across a graft union and target DNA methylation de novo at normally unmethylated sites in the genomes of root cells from a different accession.

X Demographics

X Demographics

The data shown below were collected from the profiles of 53 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 430 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 3 <1%
Germany 2 <1%
United Kingdom 2 <1%
Brazil 1 <1%
India 1 <1%
Netherlands 1 <1%
New Zealand 1 <1%
Mexico 1 <1%
Argentina 1 <1%
Other 5 1%
Unknown 412 96%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 100 23%
Researcher 96 22%
Student > Master 42 10%
Student > Postgraduate 36 8%
Student > Bachelor 28 7%
Other 65 15%
Unknown 63 15%
Readers by discipline Count As %
Agricultural and Biological Sciences 234 54%
Biochemistry, Genetics and Molecular Biology 105 24%
Medicine and Dentistry 4 <1%
Computer Science 3 <1%
Environmental Science 3 <1%
Other 15 3%
Unknown 66 15%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 83. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 09 October 2020.
All research outputs
#500,484
of 24,988,543 outputs
Outputs from Proceedings of the National Academy of Sciences of the United States of America
#8,828
of 102,105 outputs
Outputs of similar age
#9,163
of 405,942 outputs
Outputs of similar age from Proceedings of the National Academy of Sciences of the United States of America
#198
of 848 outputs
Altmetric has tracked 24,988,543 research outputs across all sources so far. Compared to these this one has done particularly well and is in the 97th percentile: it's in the top 5% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 102,105 research outputs from this source. They typically receive a lot more attention than average, with a mean Attention Score of 39.0. This one has done particularly well, scoring higher than 91% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 405,942 tracked outputs that were published within six weeks on either side of this one in any source. This one has done particularly well, scoring higher than 97% of its contemporaries.
We're also able to compare this research output to 848 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 76% of its contemporaries.