Evidence map›Paper›PMID 26061962›Full record

ArticlePloS one2015

High-Throughput Sequencing Reveals Hypothalamic MicroRNAs as Novel Partners Involved in Timing the Rapid Development of Chicken (Gallus gallus) Gonads.

Wei Han, Jianmin Zou, Kehua Wang, Yijun Su, Yunfen Zhu, Chi Song, Guohui Li, Liang Qu, Huiyong Zhang, Honglin Liu

Open 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. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-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

8 citing papers in PubMed, 16 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Wei HanCollege of Animal Science & Technology, Nanjing Agricultural University, Nanjing, PR China; National Chickens Genetic Resources, Poultry institute, Chinese Academy of Agricultural Science, Yangzhou, PR China.
Jianmin ZouNational Chickens Genetic Resources, Poultry institute, Chinese Academy of Agricultural Science, Yangzhou, PR China.
Kehua WangNational Chickens Genetic Resources, Poultry institute, Chinese Academy of Agricultural Science, Yangzhou, PR China.
Yijun SuNational Chickens Genetic Resources, Poultry institute, Chinese Academy of Agricultural Science, Yangzhou, PR China.
Yunfen ZhuNational Chickens Genetic Resources, Poultry institute, Chinese Academy of Agricultural Science, Yangzhou, PR China.
Chi SongNational Chickens Genetic Resources, Poultry institute, Chinese Academy of Agricultural Science, Yangzhou, PR China.
Guohui LiNational Chickens Genetic Resources, Poultry institute, Chinese Academy of Agricultural Science, Yangzhou, PR China.
Liang QuNational Chickens Genetic Resources, Poultry institute, Chinese Academy of Agricultural Science, Yangzhou, PR China.
Huiyong ZhangNational Chickens Genetic Resources, Poultry institute, Chinese Academy of Agricultural Science, Yangzhou, PR China.
Honglin LiuCollege of Animal Science & Technology, Nanjing Agricultural University, Nanjing, PR China.
Poultry Research Institute · CNNanjing Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Onset of the rapid gonad growth is a milestone in sexual development that comprises many genes and regulatory factors. The observations in model organisms and mammals including humans have shown a potential link between miRNAs and development timing. To determine whether miRNAs play roles in this process in the chicken (Gallus gallus), the Solexa deep sequencing was performed to analyze the profiles of miRNA expression in the hypothalamus of hens from two different pubertal stages, before onset of the rapid gonad development (BO) and after onset of the rapid gonad development (AO). 374 conserved and 46 novel miRNAs were identified as hypothalamus-expressed miRNAs in the chicken. 144 conserved miRNAs were showed to be differentially expressed (reads > 10, P < 0.05) during the transition from BO to AO. Five differentially expressed miRNAs were validated by real-time quantitative RT-PCR (qRT-PCR) method. 2013 putative genes were predicted as the targets of the 15 most differentially expressed miRNAs (fold-change > 4.0, P < 0.01). Of these genes, 7 putative circadian clock genes, Per2, Bmal1/2, Clock, Cry1/2, and Star were found to be targeted multiple times by the miRNAs. qRT-PCR revealed the basic transcription levels of these clock genes were much higher (P < 0.01) in AO than in BO. Further functional analysis suggested that these 15 miRNAs play important roles in transcriptional regulation and signal transduction pathways. The results provide new insights into miRNAs functions in timing the rapid development of chicken gonads. Considering the characteristics of miRNA functional conservation, the results will contribute to the research on puberty onset in humans.

Indexed as

AnimalsChickensCircadian Rhythm Signaling Peptides and ProteinsFemaleGonadsHypothalamusMaleMicroRNAsSexual DevelopmentCircadian Rhythm Signaling Peptides and ProteinsMicroRNAs

Identifiers

PMID26061962
PMCPMC4465036
OpenAlexW581860756

What OpenQuestion holds

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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.