Evidence map›Paper›PMID 27370822›Full record

ArticleMolecular brain2016

Disrupted-in-schizophrenia 1 (DISC1) and Syntaphilin collaborate to modulate axonal mitochondrial anchoring.

Cana Park, Seol-Ae Lee, Ji-Ho Hong, Yeongjun Suh, Sung Jin Park, Bo Kyoung Suh, Youngsik Woo, Jinhyuk Choi, Ji-Won Huh, You-Me Kim and 1 more

Abstract read
In one paragraph

Article in Molecular brain, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Gcap14 is a microtubule plus-end-tracking protein coordinating microtubule-actin crosstalk during neurodevelopment.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Mutations in DISC1 alter IPNeuronal signaling · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. DISC1 Regulates Mitochondrial Trafficking in a Miro1-GTP-Dependent Manner.Frontiers in cell and developmental biology · 2020
    Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review
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

11 authors.

Cana ParkDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea.
Seol-Ae LeeDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea.
Ji-Ho HongDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea.
Yeongjun SuhDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea.
Sung Jin ParkDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea.
Bo Kyoung SuhDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea.
Youngsik WooDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea.
Jinhyuk ChoiDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea.
Ji-Won HuhDivision of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea.
You-Me KimDivision of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea.
Sang Ki ParkDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, 790-784, Republic of Korea. skpark@postech.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In neuronal axons, the ratio of motile-to-stationary mitochondria is tightly regulated by neuronal activation, thereby meeting the need for local calcium buffering and maintaining the ATP supply. However, the molecular players and detailed regulatory mechanisms behind neuronal mitochondrial movement are not completely understood. Here, we found that neuronal activation-induced mitochondrial anchoring is regulated by Disrupted-in-schizophrenia 1 (DISC1), which is accomplished by functional association with Syntaphilin (SNPH). DISC1 deficiency resulted in reduced axonal mitochondrial movement, which was partially reversed by concomitant SNPH depletion. In addition, a SNPH deletion mutant lacking the sequence for interaction with DISC1 exhibited an enhanced mitochondrial anchoring effect than wild-type SNPH. Moreover, upon neuronal activation, mitochondrial movement was preserved by DISC1 overexpression, not showing immobilized response of mitochondria. Taken together, we propose that DISC1 in association with SNPH is a component of a modulatory complex that determines mitochondrial anchoring in response to neuronal activation.

Indexed as

AnimalsAxonsFemaleHEK293 CellsHumansMembrane ProteinsMiceMice, Inbred ICRMicrotubule-Associated ProteinsMitochondriaNerve Tissue ProteinsProtein Bindingrho GTP-Binding ProteinsDisc1 protein, mouseMembrane ProteinsMicrotubule-Associated ProteinsMiro-1 protein, mouseNerve Tissue Proteinsrho GTP-Binding ProteinsSnph protein, mouseAxonal mitochondrial anchoringDISC1SchizophreniaSNPH

Identifiers

PMID27370822
PMCPMC4930613

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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.