Evidence map›Paper›PMID 25897513›Full record

ArticlePloS one2015

A RNA-Seq Analysis of the Rat Supraoptic Nucleus Transcriptome: Effects of Salt Loading on Gene Expression.

Kory R Johnson, C C T Hindmarch, Yasmmyn D Salinas, YiJun Shi, Michael Greenwood, See Ziau Hoe, David Murphy, Harold Gainer

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2015. 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 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 3 countries.

Kory R JohnsonBioinformatics Section, Information Technology and Bioinformatics Program, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, 20892, United States of America.
C C T HindmarchSchool of Clinical Sciences, Dorothy Hodgkin Building, University of Bristol, Bristol, England, BS1 3NY; Department of Physiology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia, 50603.
Yasmmyn D SalinasLaboratory of Neurochemistry, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, 20892, United States of America.
YiJun ShiLaboratory of Neurochemistry, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, 20892, United States of America.
Michael GreenwoodSchool of Clinical Sciences, Dorothy Hodgkin Building, University of Bristol, Bristol, England, BS1 3NY.
See Ziau HoeDepartment of Physiology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia, 50603.
David MurphySchool of Clinical Sciences, Dorothy Hodgkin Building, University of Bristol, Bristol, England, BS1 3NY; Department of Physiology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia, 50603.
Harold GainerLaboratory of Neurochemistry, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, 20892, United States of America.
National Institute of Neurological Disorders and Stroke · USUniversity of Bristol · GBNational Institutes of Health · USUniversity of Malaya · MY

Funding

Biotechnology and Biological Sciences Research Council BB/J005452/1British Heart Foundation RG/11/28714British Heart Foundation RG/11/6/28714Intramural NIH HHS
6 · The paper itself

Abstract

Magnocellular neurons (MCNs) in the hypothalamo-neurohypophysial system (HNS) are highly specialized to release large amounts of arginine vasopressin (Avp) or oxytocin (Oxt) into the blood stream and play critical roles in the regulation of body fluid homeostasis. The MCNs are osmosensory neurons and are excited by exposure to hypertonic solutions and inhibited by hypotonic solutions. The MCNs respond to systemic hypertonic and hypotonic stimulation with large changes in the expression of their Avp and Oxt genes, and microarray studies have shown that these osmotic perturbations also cause large changes in global gene expression in the HNS. In this paper, we examine gene expression in the rat supraoptic nucleus (SON) under normosmotic and chronic salt-loading SL) conditions by the first time using "new-generation", RNA sequencing (RNA-Seq) methods. We reliably detect 9,709 genes as present in the SON by RNA-Seq, and 552 of these genes were changed in expression as a result of chronic SL. These genes reflect diverse functions, and 42 of these are involved in either transcriptional or translational processes. In addition, we compare the SON transcriptomes resolved by RNA-Seq methods with the SON transcriptomes determined by Affymetrix microarray methods in rats under the same osmotic conditions, and find that there are 6,466 genes present in the SON that are represented in both data sets, although 1,040 of the expressed genes were found only in the microarray data, and 2,762 of the expressed genes are selectively found in the RNA-Seq data and not the microarray data. These data provide the research community a comprehensive view of the transcriptome in the SON under normosmotic conditions and the changes in specific gene expression evoked by salt loading.

Indexed as

TranscriptomeAnimalsMaleOligonucleotide Array Sequence AnalysisRats, Sprague-DawleyRNA, MessengerSalt ToleranceSequence Analysis, RNASupraoptic NucleusWater-Electrolyte BalanceRNA, Messenger

Identifiers

PMID25897513
PMCPMC4405539
OpenAlexW2005494764

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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.