Evidence map›Paper›PMID 29970601›Full record

ArticleScience signaling2018

Proteomic analysis of S-nitrosylated nuclear proteins in rat cortical neurons.

Jacob G Smith, Sarah G Aldous, Catia Andreassi, Giovanni Cuda, Marco Gaspari, Antonella Riccio

Abstract read
In one paragraph

Article in Science signaling, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 26 citations in OpenAlex.

  1. S-Nitrosylation of CRTC1 in Alzheimer's disease impairs CREB-dependent gene expression induced by neuronal activity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. 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

6 authors at 2 institutions in 2 countries.

Jacob G SmithMedical Research Council Laboratory for Molecular Cell Biology, University College London, WC1E 6BT London, UK.ORCID 0000-0001-5139-1054
Sarah G AldousMedical Research Council Laboratory for Molecular Cell Biology, University College London, WC1E 6BT London, UK.
Catia AndreassiMedical Research Council Laboratory for Molecular Cell Biology, University College London, WC1E 6BT London, UK.ORCID 0000-0002-0541-9412
Giovanni CudaDepartment of Experimental and Clinical Medicine, University of Catanzaro, 88100 Catanzaro, Italy.ORCID 0000-0001-6313-1866
Marco GaspariDepartment of Experimental and Clinical Medicine, University of Catanzaro, 88100 Catanzaro, Italy.ORCID 0000-0002-5411-8800
Antonella RiccioMedical Research Council Laboratory for Molecular Cell Biology, University College London, WC1E 6BT London, UK. a.riccio@ucl.ac.uk.ORCID 0000-0002-1085-0629
MRC Laboratory for Molecular Cell Biology · GBMagna Graecia University · IT

Funding

Medical Research Council G0802010Medical Research Council MC_U12266BWellcome Trust 103717
6 · The paper itself

Abstract

Neurons modulate gene expression in response to extrinsic signals to enable brain development, cognition, and learning and to process stimuli that regulate systemic physiological functions. This signal-to-gene communication is facilitated by posttranslational modifications such as S-nitrosylation, the covalent attachment of a nitric oxide (NO) moiety to cysteine thiols. In the cerebral cortex, S-nitrosylation of histone deacetylase 2 (HDAC2) is required for gene transcription during neuronal development, but few other nuclear targets of S-nitrosylation have been identified to date. We used S-nitrosothiol resin-assisted capture on NO donor-treated nuclear extracts from rat cortical neurons and identified 614 S-nitrosylated nuclear proteins. Of these, 131 proteins have not previously been shown to be S-nitrosylated in any system, and 555 are previously unidentified targets of S-nitrosylation in neurons. The sites of S-nitrosylation were identified for 59% of the targets, and motifs containing single lysines were found at 33% of these sites. In addition, lysine motifs were necessary for promoting the S-nitrosylation of HDAC2 and methyl-CpG binding protein 3 (MBD3). Moreover, S-nitrosylation of the histone-binding protein RBBP7 was necessary for dendritogenesis of cortical neurons in culture. Together, our findings characterize S-nitrosylated nuclear proteins in neurons and identify S-nitrosylation motifs that may be shared with other targets of NO signaling.

Indexed as

Protein Processing, Post-TranslationalAnimalsCerebral CortexDendritesEmbryo, MammalianFemaleNeuronsNitric OxideNuclear ProteinsPregnancyProteomeRatsRats, Sprague-DawleyNitric OxideNuclear ProteinsProteome

Identifiers

PMID29970601
PMCPMC6726469
OpenAlexW2810285992

What OpenQuestion holds

Textmetadata
LicenceTDM
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.