Evidence map›Paper›PMID 27313591›Full record

ArticleFrontiers in plant science2016

Novel Meiotic miRNAs and Indications for a Role of PhasiRNAs in Meiosis.

Stefanie Dukowic-Schulze, Anitha Sundararajan, Thiruvarangan Ramaraj, Shahryar Kianian, Wojciech P Pawlowski, Joann Mudge, Changbin Chen

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Frontiers in plant science, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
21.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Reproductive phasiRNAs are the piRNAs of plants.Trends in genetics : TIG · 2026
    Review
  3. Article
  4. Epigenetics in the modern era of crop improvements.Science China. Life sciences · 2025
    Review
  5. Review
  6. Article
  7. DNA methylation dynamics during germline development.Journal of integrative plant biology · 2022
    Review
  8. Article
  9. Epigenetic Dynamics and Regulation of Plant Male Reproduction.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Stefanie Dukowic-SchulzeDepartment of Horticultural Science, University of Minnesota, St. Paul MN, USA.
Anitha SundararajanNational Center for Genome Resources, Santa Fe NM, USA.
Thiruvarangan RamarajNational Center for Genome Resources, Santa Fe NM, USA.
Shahryar KianianCereal Disease Laboratory, United States Department of Agriculture - Agricultural Research Service, St. Paul MN, USA.
Wojciech P PawlowskiSection of Plant Biology, School of Integrative Plant Science, Cornell University, Ithaca NY, USA.
Joann MudgeNational Center for Genome Resources, Santa Fe NM, USA.
Changbin ChenDepartment of Horticultural Science, University of Minnesota, St. Paul MN, USA.
National Center for Genome Resources · USUniversity of Minnesota · USCereal Disease Laboratory · USCornell University · US

Funding

NM-INBRE Sequencing and Bioinformatics CoreP20GM103451 · NIGMS · NEW MEXICO STATE UNIVERSITY LAS CRUCES · PI Charlotte C. Gard · 2012 to 2026
$61.2M
NIGMS NIH HHS P20 GM103451
6 · The paper itself

Abstract

Small RNAs (sRNA) add additional layers to the regulation of gene expression, with siRNAs directing gene silencing at the DNA level by RdDM (RNA-directed DNA methylation), and micro RNAs (miRNAs) directing post-transcriptional regulation of specific target genes, mostly by mRNA cleavage. We used manually isolated male meiocytes from maize (Zea mays) to investigate sRNA and DNA methylation landscapes during zygotene, an early stage of meiosis during which steps of meiotic recombination and synapsis of paired homologous chromosomes take place. We discovered two novel miRNAs from meiocytes, zma-MIR11969 and zma-MIR11970, and identified putative target genes. Furthermore, we detected abundant phasiRNAs of 21 and 24 nt length. PhasiRNAs are phased small RNAs which occur in 21 or 24 nt intervals, at a few hundred loci, specifically in male reproductive tissues in grasses. So far, the function of phasiRNAs remained elusive. Data from isolated meiocytes now revealed elevated DNA methylation at phasiRNA loci, especially in the CHH context, suggesting a role for phasiRNAs in cis DNA methylation. In addition, we consider a role of these phasiRNAs in chromatin remodeling/dynamics during meiosis. However, this is not well supported yet and will need more additional data. Here, we only lay out the idea due to other relevant literature and our additional observation of a peculiar GC content pattern at phasiRNA loci. Chromatin remodeling is also indicated by the discovery that histone genes were enriched for sRNA of 22 nt length. Taken together, we gained clues that lead us to hypothesize sRNA-driven DNA methylation and possibly chromatin remodeling during male meiosis in the monocot maize which is in line with and extends previous knowledge.

Indexed as

bisulfite sequencingDNA methylationmaizemeiocytesmeiosisphasiRNAsmall RNAsRNA-seq

Identifiers

PMID27313591
PMCPMC4889585
OpenAlexW2420853899

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.