Evidence map›Paper›PMID 27119337›Full record

ArticlePloS one2016

Differential Expression of Long Noncoding RNAs between Sperm Samples from Diabetic and Non-Diabetic Mice.

Guang-Jian Jiang, Teng Zhang, Tian An, Dan-Dan Zhao, Xiu-Yan Yang, Dong-Wei Zhang, Yi Zhang, Qian-Qian Mu, Na Yu, Xue-Shan Ma and 1 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2016. 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
2.4field-weighted citation impact, top 13% 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, 30 citations in OpenAlex.

  1. Review
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  9. Long non-coding RNA MEG3 mediates high glucose-induced endothelial cell dysfunction.International journal of clinical and experimental pathology · 2018
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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

11 authors at 3 institutions in 1 country.

Guang-Jian JiangDiabetes Research Center of Beijing University of Chinese Medicine, Beijing, China.
Teng ZhangState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Tian AnDiabetes Research Center of Beijing University of Chinese Medicine, Beijing, China.
Dan-Dan ZhaoDiabetes Research Center of Beijing University of Chinese Medicine, Beijing, China.
Xiu-Yan YangDiabetes Research Center of Beijing University of Chinese Medicine, Beijing, China.
Dong-Wei ZhangDiabetes Research Center of Beijing University of Chinese Medicine, Beijing, China.
Yi ZhangDiabetes Research Center of Beijing University of Chinese Medicine, Beijing, China.
Qian-Qian MuDiabetes Research Center of Beijing University of Chinese Medicine, Beijing, China.
Na YuDiabetes Research Center of Beijing University of Chinese Medicine, Beijing, China.
Xue-Shan MaState Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Si-Hua GaoDiabetes Research Center of Beijing University of Chinese Medicine, Beijing, China.
Beijing University of Chinese Medicine · CNChinese Academy of Sciences · CNInstitute of Zoology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate the potential core reproduction-related genes associated with the development of diabetes, the expression profiles of long noncoding RNA (lncRNA) and messenger RNA (mRNA) in the sperm of diabetic mice were studied. We used microarray analysis to detect the expression of lncRNAs and coding transcripts in six diabetic and six normal sperm samples, and differentially expressed lncRNAs and mRNAs were identified through Volcano Plot filtering. The function of differentially expressed mRNA was determined by pathway and gene ontology (GO) analysis, and the function of lncRNAs was studied by subgroup analysis and their physical or functional relationships with corresponding mRNAs. A total of 7721 lncRNAs and 6097 mRNAs were found to be differentially expressed between the diabetic and normal sperm groups. The diabetic sperm exhibited aberrant expression profiles for lncRNAs and mRNAs, and GO and pathway analyses showed that the functions of differentially expressed mRNAs were closely related with many processes involved in the development of diabetes. Furthermore, potential core genes that might play important roles in the pathogenesis of diabetes-related low fertility were revealed by lncRNA- and mRNA-interaction studies, as well as coding-noncoding gene co-expression analysis based on the microarray expression profiles.

Indexed as

AnimalsDiabetes Mellitus, ExperimentalMaleMiceMice, Inbred C57BLRNA, Long NoncodingRNA, MessengerSpermatozoaRNA, Long NoncodingRNA, Messenger

Identifiers

PMID27119337
PMCPMC4847876
OpenAlexW2342823001

What OpenQuestion holds

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LicenceCC BY
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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.