Evidence map›Paper›PMID 31432767›Full record

ArticleRNA biology2019

Deep sequencing of small non-coding RNA highlights brain-specific expression patterns and RNA cleavage.

Fiete Haack, Nares Trakooljul, Kevin Gley, Eduard Murani, Frieder Hadlich, Klaus Wimmers, Siriluck Ponsuksili

Open access · greenAbstract read
In one paragraph

Article in RNA biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.4field-weighted citation impact, top 45% 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

13 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Emerging roles of transfer RNA fragments in the CNS.Brain : a journal of neurology · 2025
    Review
  6. Hallmarks of Brain Plasticity.Biomedicines · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Editorial: Small non-coding RNAs in diseases.Frontiers in molecular biosciences · 2022
    Article
  13. Article
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

7 authors at 1 institution in 1 country.

Fiete HaackInstitute for Genome Biology, Functional Genome Analysis Research Unit, Leibniz Institute for Farm Animal Biology (FBN), Dummerstorf, Germany.
Nares TrakooljulInstitute for Genome Biology, Genomics Research Unit, Leibniz Institute for Farm Animal Biology (FBN), Dummerstorf, Germany.
Kevin GleyInstitute for Genome Biology, Functional Genome Analysis Research Unit, Leibniz Institute for Farm Animal Biology (FBN), Dummerstorf, Germany.
Eduard MuraniInstitute for Genome Biology, Genomics Research Unit, Leibniz Institute for Farm Animal Biology (FBN), Dummerstorf, Germany.ORCID 0000-0002-3939-6255
Frieder HadlichInstitute for Genome Biology, Functional Genome Analysis Research Unit, Leibniz Institute for Farm Animal Biology (FBN), Dummerstorf, Germany.ORCID 0000-0002-1158-4860
Klaus WimmersInstitute for Genome Biology, Genomics Research Unit, Leibniz Institute for Farm Animal Biology (FBN), Dummerstorf, Germany.
Siriluck PonsuksiliInstitute for Genome Biology, Functional Genome Analysis Research Unit, Leibniz Institute for Farm Animal Biology (FBN), Dummerstorf, Germany.
Research Institute for Farm Animal Biology (FBN) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the advance of high-throughput sequencing technology numerous new regulatory small RNAs have been identified, that broaden the variety of processing mechanisms and functions of non-coding RNA. Here we explore small non-coding RNA (sncRNA) expression in central parts of the physiological stress and anxiety response system. Therefore, we characterize the sncRNA profile of tissue samples from Amygdala, Hippocampus, Hypothalamus and Adrenal Gland, obtained from 20 pigs. Our analysis reveals that all tissues but Amygdala and Hippocampus possess distinct, tissue-specific expression pattern of miRNA that are associated with Hypoxia, stress responses as well as memory and fear conditioning. In particular, we observe marked differences in the expression profile of limbic tissues compared to those associated to the HPA/stress axis, with a surprisingly high aggregation of 3´-tRNA halves in Amygdala and Hippocampus. Since regulation of sncRNA and RNA cleavage plays a pivotal role in the central nervous system, our work provides seminal insights in the role/involvement of sncRNA in the transcriptional and post-transcriptional regulation of negative emotion, stress and coping behaviour in pigs, and mammals in general.

Indexed as

Gene Expression RegulationGenomeAdaptation, PhysiologicalAdrenal GlandsAmygdalaAnimalsConditioning, OperantFearHigh-Throughput Nucleotide SequencingHippocampusHypothalamusHypoxiaMemoryMolecular Sequence AnnotationOrgan SpecificityRNA CleavageRNA, Small Untranslated3´-tiRNA5´-tiRNAAmygdalaHippocampusHPA axisSncrna

Identifiers

PMID31432767
PMCPMC6844574
OpenAlexW2969212211

What OpenQuestion holds

Textmetadata
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.