Evidence map›Paper›PMID 29294243›Full record

ArticleMolecular neurobiology2018

A Novel Short Isoform of Cytosolic PSD-95 Interactor (Cypin) Regulates Neuronal Development.

Mihir V Patel, Przemyslaw Swiatkowski, Munjin Kwon, Ana R Rodriguez, Keith Campagno, Bonnie L Firestein

Open access · greenAbstract read
In one paragraph

Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed, 14 citations in OpenAlex.

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  9. Autoantibody-associated psychiatric syndromes in children: link to adult psychiatry.Journal of neural transmission (Vienna, Austria : 1996) · 2021
    Review
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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

6 authors at 1 institution in 1 country.

Mihir V PatelDepartment of Cell Biology and Neuroscience, Rutgers University (USA), 604 Allison Road, Piscataway, NJ, 08854-8082, USA.
Przemyslaw SwiatkowskiDepartment of Cell Biology and Neuroscience, Rutgers University (USA), 604 Allison Road, Piscataway, NJ, 08854-8082, USA.
Munjin KwonDepartment of Cell Biology and Neuroscience, Rutgers University (USA), 604 Allison Road, Piscataway, NJ, 08854-8082, USA.
Ana R RodriguezDepartment of Cell Biology and Neuroscience, Rutgers University (USA), 604 Allison Road, Piscataway, NJ, 08854-8082, USA.
Keith CampagnoDepartment of Cell Biology and Neuroscience, Rutgers University (USA), 604 Allison Road, Piscataway, NJ, 08854-8082, USA.
Bonnie L FiresteinDepartment of Cell Biology and Neuroscience, Rutgers University (USA), 604 Allison Road, Piscataway, NJ, 08854-8082, USA. firestein@biology.rutgers.edu.
Rutgers, The State University of New Jersey · US

Funding

UMDNJ TRAINING GRANT IN BIOTECHNOLOGYT32GM008339 · NIGMS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI YARMUSH, MARTIN L · 1989 to 2019
$6.1M
National Institute of General Medical Sciences T32 GM008339-20National Science Foundation IOS-1353724New Jersey Commission on Brain Injury Research CBIR15FEL009New Jersey Commission on Brain Injury Research CBIR16FEL013NIGMS NIH HHS T32 GM008339Rutgers, The State University of New Jersey Aresty Research Fellowship
6 · The paper itself

Abstract

The guanine deaminase cypin (cytosolic PSD-95 interactor) binds to PSD-95 (postsynaptic density protein 95) and regulates dendrite branching by promoting microtubule polymerization. Here, we identify a novel short isoform of cypin, termed cypinS, which is expressed in mouse and human, but not rat, tissues. Cypin and cypinS mRNA and protein levels peak at P7 and P14 in the mouse brain, suggesting a role for these isoforms during development. Interestingly, although cypinS lacks guanine deaminase activity, overexpression of cypinS increases dendrite branching. This increase occurs further away from soma than do increases resulting from overexpression of cypin. In contrast, overexpression of cypin, but not cypinS, decreases dendritic spine density and maturity. This suggests that changes to spines, but not to dendrites, may be dependent on guanine deaminase activity. Furthermore, overexpression of either cypin or cypinS increases miniature excitatory postsynaptic current (mEPSC) frequency, pointing to a presynaptic role for both isoforms. Interestingly, overexpression of cypinS results in a significantly greater increase in frequency than does overexpression of cypin. Thus, cypin and cypinS play distinct roles in neuronal development.

Indexed as

AnimalsBrainChlorocebus aethiopsCOS CellsDendritesDisks Large Homolog 4 ProteinExcitatory Postsynaptic PotentialsGuanine DeaminaseHEK293 CellsHippocampusHumansMiceNeuronsOrgan SpecificityProtein IsoformsRNA, MessengerDisks Large Homolog 4 ProteinGDA protein, mouseGuanine DeaminaseProtein IsoformsRNA, MessengerCell cultureCypinDendriteDendritic spineElectrophysiologyMorphologyNeuron

Identifiers

PMID29294243
PMCPMC6028325
OpenAlexW2782515950

What OpenQuestion holds

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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.