Evidence map›Paper›PMID 30604382›Full record

ArticleJournal of molecular neuroscience : MN2019

Network Profiling of Brain-Expressed X-Chromosomal MicroRNA Genes Implicates Shared Key MicroRNAs in Intellectual Disability.

Thainá Fernandez Gonçalves, Rafael Mina Piergiorge, Jussara Mendonça Dos Santos, Jaqueline Gusmão, Márcia Mattos Gonçalves Pimentel, Cíntia Barros Santos-Rebouças

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In one paragraph

Article in Journal of molecular neuroscience : MN, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  8. What microRNAs could tell us about the human X chromosome.Cellular and molecular life sciences : CMLS · 2020
    Review
  9. Review
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

6 authors at 2 institutions in 1 country.

Thainá Fernandez GonçalvesServgen, Department of Genetics, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Rafael Mina PiergiorgeFunctional Genomics and Bioinformatics Laboratory, Fiocruz, Oswaldo Cruz Institute, Rio de Janeiro, Brazil.
Jussara Mendonça Dos SantosServgen, Department of Genetics, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Jaqueline GusmãoLaboratory of Fisheries Genetics and Conservation, Department of Genetics, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Márcia Mattos Gonçalves PimentelServgen, Department of Genetics, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Cíntia Barros Santos-RebouçasServgen, Department of Genetics, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro, Rio de Janeiro, Brazil. cbs@uerj.br.ORCID http://orcid.org/0000-0003-4729-2373
Universidade do Estado do Rio de Janeiro · BRFundação Oswaldo Cruz · BR

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior FELLOWSHIPFundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro faperj
6 · The paper itself

Abstract

MicroRNAs are endogenous non-protein-coding RNA molecules that regulate post-transcriptional gene expression. The majority of human miRNAs are brain-expressed and chromosome X is enriched in miRNA genes. We analyzed the genomic regions of 12 brain-expressed pre-miRNAs located on chromosome X coding for 18 mature miRNAs, aiming to investigate the involvement of miRNA sequence variants on X-linked intellectual disability (XLID). Genomic DNA samples from 135 unrelated Brazilian males with intellectual disability, suggestive of X-linked inheritance, were amplified through polymerase chain reaction and sequenced by Sanger sequencing. Although no sequence variations have been identified, suggesting an intense selective pressure, further computational analysis evidenced that eight mature miRNAs (miR-221-3p/222-3p, miR-223-3p, miR-361-5p, miR-362-5p, miR-504-5p.1, miR-505-3p.1, and miR-505-3p.2) act as critical regulators of X-linked and autosomal ID genes in a fully connected network. Enrichment approaches identify transcription regulation, nervous system development, and regulation of cell proliferation as the main common biological processes among the target ID genes. Besides, a clustered chromosomal coverage of the imputed miRNAs target genes and related regulators was found on X chromosome. Considering the role of miRNAs as fine-tuning regulators of gene expression, a systematic analysis of miRNAs' expression could uncover part of the genetic landscape subjacent to ID, being urgently necessary in patients with this condition, particularly XLID.

Indexed as

Gene Regulatory NetworksAdolescentAdultBrainChildChild, PreschoolChromosomes, Human, XGenetic Diseases, X-LinkedHumansIntellectual DisabilityMaleMicroRNAsPolymorphism, GeneticMicroRNAsBrainChromosome XIntellectual disabilityMicroRNA

Identifiers

PMID30604382
OpenAlexW2907064895

What OpenQuestion holds

Textmetadata
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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.