Evidence map›Paper›PMID 40667103›Full record

ArticlebioRxiv : the preprint server for biology2025

Interactome Analysis of the CC2D1A Scaffold Reveals Novel Neuronal Interactions and a Postsynaptic Role.

Abigail T Heller, Aniket Bhattacharya, Haorong Li, Luka Turkalj, Shruthi Thiyagarajan, Emma Suzuki, Adele Mossa, Haiyan Zheng, Ling Hao, M Chiara Manzini

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Abigail T HellerDepartment of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, Child Health Institute of New Jersey, New Brunswick, NJ 08901, USA.ORCID 0000-0001-9589-7209
Aniket BhattacharyaDepartment of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, Child Health Institute of New Jersey, New Brunswick, NJ 08901, USA.ORCID 0000-0002-6479-3981
Haorong LiDepartment of Chemistry, The George Washington University, Washington, D.C. 20052, USA.ORCID 0000-0002-0503-4870
Luka TurkaljDepartment of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, Child Health Institute of New Jersey, New Brunswick, NJ 08901, USA.ORCID 0000-0003-3231-834X
Shruthi ThiyagarajanDepartment of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, Child Health Institute of New Jersey, New Brunswick, NJ 08901, USA.
Emma SuzukiDepartment of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, Child Health Institute of New Jersey, New Brunswick, NJ 08901, USA.
Adele MossaDepartment of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, Child Health Institute of New Jersey, New Brunswick, NJ 08901, USA.ORCID 0000-0001-6573-1101
Haiyan ZhengCenter for Advanced Biotechnology and Medicine, Rutgers Biomedical Health Sciences, Piscataway, NJ 08854, USA.
Ling HaoDepartment of Chemistry & Biochemistry, University of Maryland, College Park, MD 20742, USA.ORCID 0000-0002-0106-5266
M Chiara ManziniDepartment of Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, Child Health Institute of New Jersey, New Brunswick, NJ 08901, USA.ORCID 0000-0001-7175-1096

Funding

Defining the molecular mechanisms of sex differences in cognitive functionR01NS105000 · NINDS · RBHS-ROBERT WOOD JOHNSON MEDICAL SCHOOL · PI MANZINI, M. CHIARA · 2018 to 2022
$2.1M
NINDS NIH HHS R01 NS105000
6 · The paper itself

Abstract

Loss of the protein scaffold Coiled-coil and C2 domain containing 1A (CC2D1A) leads to intellectual disability (ID), autism spectrum disorder (ASD), and other neurodevelopmental presentations in humans. CC2D1A interactions have been studied in different cell lines proposing diverse roles in endolysosomal maturation and intracellular signaling, but the composition and functional mechanisms of the CC2D1A interactome remain poorly understood, especially in the brain. We performed comprehensive proteomic analyses to characterize CC2D1A binding partners, first comparing immunoprecipitations with three different anti-CC2D1A antibodies in HEK293 cells and then probing the mouse hippocampus. In HEK cells, Gene Ontology (GO) analysis revealed broad interaction networks in the nucleus, mitochondrion, and cytoplasmic vesicles sharing functions in organelle organization, vesicle mediated transport, and protein metabolism. These are unified by the best characterized CC2D1A interactor, the ESCRT III component CHMP4B, and define a pleiotropic role for CC2D1A in membrane trafficking and protein homeostasis. In the hippocampus, using stringent criteria and additional controls, including a

Identifiers

PMID40667103
PMCPMC12262349

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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.