Evidence map›Paper›PMID 35351830›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2022

Evolution Increases Primates Brain Complexity Extending RbFOX1 Splicing Activity to LSD1 Modulation.

Chiara Forastieri, Maria Italia, Emanuela Toffolo, Elena Romito, Maria Paola Bonasoni, Valeria Ranzani, Beatrice Bodega, Francesco Rusconi, Elena Battaglioli

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 3 institutions in 1 country.

Chiara ForastieriDepartment of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano, Segrate, 20090, Italy.
Maria ItaliaDepartment of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano, Segrate, 20090, Italy.ORCID https://orcid.org/0000-0001-6386-2466
Emanuela ToffoloDepartment of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano, Segrate, 20090, Italy.
Elena RomitoDepartment of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano, Segrate, 20090, Italy.
Maria Paola BonasoniASMN Santa Maria Nuova, Reggio Emilia, 42123, Italy.
Valeria RanzaniIstituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi," Milano, 20122, Italy.
Beatrice BodegaIstituto Nazionale di Genetica Molecolare "Romeo ed Enrica Invernizzi," Milano, 20122, Italy.
Francesco RusconiDepartment of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano, Segrate, 20090, Italy elena.battaglioli@unimi.it francesco.rusconi@unimi.it.
Elena BattaglioliDepartment of Medical Biotechnology and Translational Medicine, Università degli Studi di Milano, Segrate, 20090, Italy elena.battaglioli@unimi.it francesco.rusconi@unimi.it.
University of Milan · ITIstituto Nazionale Genetica Molecolare · ITSanta Maria Nuova Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent branching (100 MYA) of the mammalian evolutionary tree has enhanced brain complexity and functions at the putative cost of increased emotional circuitry vulnerability. Thus, to better understand psychopathology, a burden for the modern society, novel approaches should exploit evolutionary aspects of psychiatric-relevant molecular pathways. A handful of genes is nowadays tightly associated to psychiatric disorders. Among them, neuronal-enriched RbFOX1 modifies the activity of synaptic regulators in response to neuronal activity, keeping excitability within healthy domains. We here dissect a higher primates-restricted interaction between RbFOX1 and the transcriptional corepressor Lysine Specific Demethylase 1 (LSD1/KDM1A). A single nucleotide variation (AA to AG) in

Indexed as

Alternative SplicingLysineAnimalsBrainHistone DemethylasesHumansMaleMammalsMicePrimatesRepressor ProteinsRNA Splicing FactorsHistone DemethylasesKDM1A protein, humanLysineRBFOX1 protein, humanRbfox1 protein, mouseRBFOX2 protein, humanRbfox2 protein, mouseRepressor ProteinsRNA Splicing Factorsevolutionlysine specific demethylase 1major depressive disordernon-sense-mediated decaypsychiatric disordersRNA-binding Fox homolog 1

Identifiers

PMID35351830
PMCPMC9087731
OpenAlexW4220656925

What OpenQuestion holds

Textmetadata
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.