Evidence map›Paper›PMID 36205081›Full record

ArticleMolecular biology and evolution2022

A Novel Gene Controls a New Structure: PiggyBac Transposable Element-Derived 1, Unique to Mammals, Controls Mammal-Specific Neuronal Paraspeckles.

Tamás Raskó, Amit Pande, Kathrin Radscheit, Annika Zink, Manvendra Singh, Christian Sommer, Gerda Wachtl, Orsolya Kolacsek, Gizem Inak, Attila Szvetnik and 8 more

Open access · goldAbstract read
In one paragraph

Article in Molecular biology and evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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  5. Functional Characterization of the N-Terminal Disordered Region of theInternational journal of molecular sciences · 2022
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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

18 authors at 7 institutions in 4 countries.

Tamás RaskóMax Delbrück Center for Molecular Medicine in the Helmholtz Society, Berlin, Germany.
Amit PandeMax Delbrück Center for Molecular Medicine in the Helmholtz Society, Berlin, Germany.
Kathrin RadscheitMax Delbrück Center for Molecular Medicine in the Helmholtz Society, Berlin, Germany.
Annika ZinkDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, Heinrich Heine University, Duesseldorf, Germany.
Manvendra SinghMax Delbrück Center for Molecular Medicine in the Helmholtz Society, Berlin, Germany.ORCID 0000-0002-8626-5418
Christian SommerMax Delbrück Center for Molecular Medicine in the Helmholtz Society, Berlin, Germany.
Gerda WachtlInstitute of Enzymology, Research Centre for Natural Sciences, ELKH, Budapest, Hungary.
Orsolya KolacsekInstitute of Enzymology, Research Centre for Natural Sciences, ELKH, Budapest, Hungary.
Gizem InakDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, Heinrich Heine University, Duesseldorf, Germany.
Attila SzvetnikMax Delbrück Center for Molecular Medicine in the Helmholtz Society, Berlin, Germany.
Spyros PetrakisInstitute of Applied Biosciences/Centre for Research and Technology Hellas, 57001 Thessaloniki, Greece.
Mario BunseMax Delbrück Center for Molecular Medicine in the Helmholtz Society, Berlin, Germany.
Vikas BansalBiomedical Data Science and Machine Learning Group, German Center for Neurodegenerative Diseases, Tübingen 72076, Germany.
Matthias SelbachMax Delbrück Center for Molecular Medicine in the Helmholtz Society, Berlin, Germany.
Tamás I OrbánInstitute of Enzymology, Research Centre for Natural Sciences, ELKH, Budapest, Hungary.
Alessandro PrigioneDepartment of General Pediatrics, Neonatology and Pediatric Cardiology, Medical Faculty, Heinrich Heine University, Duesseldorf, Germany.
Laurence D HurstMilner Centre for Evolution, Department of Biology and Biochemistry, University of Bath, Bath, UK.ORCID 0000-0002-1002-1054
Zsuzsanna IzsvákMax Delbrück Center for Molecular Medicine in the Helmholtz Society, Berlin, Germany.
Max Delbrück Center · DEHeinrich Heine University Düsseldorf · DEInstitute of Molecular Life Sciences · HUCentre for Research and Technology Hellas · GREötvös Loránd University · HUGerman Center for Neurodegenerative Diseases · DEUniversity of Bath · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although new genes can arrive from modes other than duplication, few examples are well characterized. Given high expression in some human brain subregions and a putative link to psychological disorders [e.g., schizophrenia (SCZ)], suggestive of brain functionality, here we characterize piggyBac transposable element-derived 1 (PGBD1). PGBD1 is nonmonotreme mammal-specific and under purifying selection, consistent with functionality. The gene body of human PGBD1 retains much of the original DNA transposon but has additionally captured SCAN and KRAB domains. Despite gene body retention, PGBD1 has lost transposition abilities, thus transposase functionality is absent. PGBD1 no longer recognizes piggyBac transposon-like inverted repeats, nonetheless PGBD1 has DNA binding activity. Genome scale analysis identifies enrichment of binding sites in and around genes involved in neuronal development, with association with both histone activating and repressing marks. We focus on one of the repressed genes, the long noncoding RNA NEAT1, also dysregulated in SCZ, the core structural RNA of paraspeckles. DNA binding assays confirm specific binding of PGBD1 both in the NEAT1 promoter and in the gene body. Depletion of PGBD1 in neuronal progenitor cells (NPCs) results in increased NEAT1/paraspeckles and differentiation. We conclude that PGBD1 has evolved core regulatory functionality for the maintenance of NPCs. As paraspeckles are a mammal-specific structure, the results presented here show a rare example of the evolution of a novel gene coupled to the evolution of a contemporaneous new structure.

Indexed as

DNA Transposable ElementsRNA, Long NoncodingAnimalsCell NucleusHistonesHumansMammalsNerve Tissue ProteinsParaspecklesTransposasesDNA Transposable ElementsHistonesNerve Tissue ProteinsPGBD1 protein, humanRNA, Long NoncodingTransposasescerebellumdomesticationevolutionKRABNEAT1novel geneparaspecklePiggyBac transposonSCANtranscriptional controltransposase

Identifiers

PMID36205081
PMCPMC9538788
OpenAlexW4303199389

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.