Evidence map›Paper›PMID 29954327›Full record

ArticleBMC genomics2018

Identification and differential regulation of microRNAs during thyroid hormone-dependent metamorphosis in Microhyla fissipes.

Lusha Liu, Wei Zhu, Jiongyu Liu, Shouhong Wang, Jianping Jiang

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Homosalate and ERK Knockdown in the Modulation ofCurrent issues in molecular biology · 2024
    Article
  2. Article
  3. Mechanisms ofGenes · 2022
    Article
  4. 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

5 authors at 1 institution in 1 country.

Lusha LiuChengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, 610041, China. liuls@cib.ac.cn.ORCID http://orcid.org/0000-0001-5935-4821
Wei ZhuChengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, 610041, China.
Jiongyu LiuChengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, 610041, China.
Shouhong WangChengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, 610041, China.
Jianping JiangChengdu Institute of Biology, Chinese Academy of Sciences, Chengdu, 610041, China. jiangjp@cib.ac.cn.
Chinese Academy of Sciences · CN

Funding

Important Research Project of Chinese Academy of Sciences KJZG-EW-L13Western Light Talent Culture Project of the Chinese Academy of Sciences 2015XBZG_XBQNXZ_B_011
6 · The paper itself

Abstract

backgroundAnuran metamorphosis, which is obligatorily initiated and sustained by thyroid hormone (TH), is a dramatic example of extensive morphological, biochemical and cellular changes occurring during post-embryonic development. Thus, it provides an ideal model to understand the actions of the hormone and molecular mechanisms underlying these developmental and apoptotic processes. In addition to transcriptional factors, microRNAs (miRNAs) play key roles in diverse biological processes via post-transcriptional repression of mRNAs. However, the possible role of miRNAs in anuran metamorphosis is not well understood. Screening and identification of TH-responding miRNAs are required to reveal the integrated regulatory mechanisms of TH during metamorphosis. Given the specific role of TRs during M. fissipes metamorphosis and the characteristics of M. fissipes as an ideal model, Illumina sequencing technology was employed to get a full scope of miRNA in M. fissipes metamorphosis treated by T3.

resultsMorphological and histological analysis revealed that 24 h T3 treatment M. fissipes tadpoles resembled that at the climax of natural metamorphosis. Thus, small RNA libraries were constructed from control and 24 h T3 treatment groups. A total of 164 conserved miRNAs and 36 predicted novel miRNAs were characterized. Furthermore, 5' first and ninth nucleotides of miRNAs were significantly enriched in U in our study. In all, 21 miRNAs were differentially expressed between the T3 and control groups (p < 0.01). A total of 10,206 unigenes were identified as target genes of these differentially expressed miRNAs. KEGG pathway analysis indicated that the most overrepresented miRNA target genes were enriched in the "PI3k-Akt signaling pathway". In addition, a network associated with the TH signaling pathway provides an opportunity to further understand the complex biological processes that occur in metamorphosis.

conclusionsWe identified a large number of miRNAs during M. fissipes metamorphosis, and 21 of them were differentially expressed in the two groups that represented two different metamorphic stages. These miRNAs may play important roles during metamorphosis. The study gives us clues for further studies of the mechanisms of anuran metamorphosis and provides a model to study the mechanism of TH-affected biological processes in humans.

Indexed as

AnimalsAnuraFemaleGene Expression Regulation, DevelopmentalIntestinesLarvaMaleMetamorphosis, BiologicalMicroRNAsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionThyroid HormonesTriiodothyronineMicroRNAsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktThyroid HormonesTriiodothyronineHistologyMetamorphosisMicrohyla fissipesmiRNAMorphologyTarget geneTH

Identifiers

PMID29954327
PMCPMC6025837
OpenAlexW2810313860

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.