Evidence map›Paper›PMID 28119418›Full record

ArticleNucleic acids research2017

Nucleoid and cytoplasmic localization of small RNAs in Escherichia coli.

Huanjie Sheng, Weston T Stauffer, Razika Hussein, Chris Lin, Han N Lim

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. A Safe and Versatile Minicell Platform Derived fromJournal of microbiology and biotechnology · 2025
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  4. Review
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  6. Article
  7. Three Microbial Musketeers of the Seas:International journal of molecular sciences · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. RNA Localization in Bacteria.Microbiology spectrum · 2018
    Review
  15. RNA search engines empower the bacterial intranet.Biochemical Society transactions · 2017
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Huanjie ShengDepartment of Integrative Biology, 3060 Valley Life Sciences Building, Mail code 3140, University of California, Berkeley, CA, 94720-3140, USA.
Weston T StaufferDepartment of Integrative Biology, 3060 Valley Life Sciences Building, Mail code 3140, University of California, Berkeley, CA, 94720-3140, USA.
Razika HusseinDepartment of Integrative Biology, 3060 Valley Life Sciences Building, Mail code 3140, University of California, Berkeley, CA, 94720-3140, USA.
Chris LinDepartment of Integrative Biology, 3060 Valley Life Sciences Building, Mail code 3140, University of California, Berkeley, CA, 94720-3140, USA.
Han N LimDepartment of Integrative Biology, 3060 Valley Life Sciences Building, Mail code 3140, University of California, Berkeley, CA, 94720-3140, USA.
University of California, Berkeley · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial small RNAs (sRNAs) regulate protein production by binding to mRNAs and altering their translation and degradation. sRNAs are smaller than most mRNAs but larger than many proteins. Therefore it is uncertain whether sRNAs can enter the nucleoid to target nascent mRNAs. Here, we investigate the intracellular localization of sRNAs transcribed from plasmids in Escherichia coli using RNA fluorescent in-situ hybridization. We found that sRNAs (GlmZ, OxyS, RyhB and SgrS) have equal preference for the nucleoid and cytoplasm, and no preferential localization at the cell membrane. We show using the gfp mRNA (encoding green fluorescent protein) that non-sRNAs can be engineered to have different proportions of nucleoid and cytoplasmic localization by altering their length and/or translation. The same localization as sRNAs was achieved by decreasing gfp mRNA length and translation, which suggests that sRNAs and other RNAs may enter the densely packed DNA of the nucleoid if they are sufficiently small. We also found that the Hfq protein, which binds sRNAs, minimally affects sRNA localization. Important implications of our findings for engineering synthetic circuits are: (i) sRNAs can potentially bind nascent mRNAs in the nucleoid, and (ii) localization patterns and distribution volumes of sRNAs can differ from some larger RNAs.

Indexed as

Cell MembraneEscherichia coliEscherichia coli ProteinsHost Factor 1 ProteinProtein BiosynthesisRNA, BacterialRNA, Small CytoplasmicRNA, Small UntranslatedEscherichia coli ProteinsHfq protein, E coliHost Factor 1 ProteinRNA, BacterialRNA, Small CytoplasmicRNA, Small Untranslated

Identifiers

PMID28119418
PMCPMC5389542
OpenAlexW2582750616

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.