Evidence map›Paper›PMID 27889896›Full record

ArticleMolecular neurobiology2017

Decreased Anxiety-Related Behaviour but Apparently Unperturbed NUMB Function in Ligand of NUMB Protein-X (LNX) 1/2 Double Knockout Mice.

Joan A Lenihan, Orthis Saha, Victoria Heimer-McGinn, John F Cryan, Guoping Feng, Paul W Young

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2017. 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
0.9field-weighted citation impact, top 23% 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, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Identifying key mFrontiers in genetics · 2022
    Article
  7. Review
  8. Liprin-α-Mediated Assemblies and Their Roles in Synapse Formation.Frontiers in cell and developmental biology · 2021
    Review
  9. Article
  10. Review
  11. Article
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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 3 institutions in 4 countries.

Joan A LenihanSchool of Biochemistry and Cell Biology, University College Cork, Cork, Ireland.
Orthis SahaSchool of Biochemistry and Cell Biology, University College Cork, Cork, Ireland.
Victoria Heimer-McGinnSchool of Biochemistry and Cell Biology, University College Cork, Cork, Ireland.
John F CryanDepartment of Anatomy and Neuroscience, University College Cork, Cork, Ireland.
Guoping FengMcGovern Institute for Brain Research, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Paul W YoungSchool of Biochemistry and Cell Biology, University College Cork, Cork, Ireland. p.young@ucc.ie.
University College Cork · IEÉcole Normale Supérieure - PSL · FRMassachusetts Institute of Technology · US

Funding

Irish Research Council Postgraduate ScholarshipScience Foundation Ireland (IE) 08/RFP/NSC1382
6 · The paper itself

Abstract

NUMB is a key regulator of neurogenesis and neuronal differentiation that can be ubiquitinated and targeted for proteasomal degradation by ligand of numb protein-X (LNX) family E3 ubiquitin ligases. However, our understanding of LNX protein function in vivo is very limited. To examine the role of LNX proteins in regulating NUMB function in vivo, we generated mice lacking both LNX1 and LNX2 expression in the brain. Surprisingly, these mice are healthy, exhibit unaltered levels of NUMB protein and do not display any neuroanatomical defects indicative of aberrant NUMB function. Behavioural analysis of LNX1/LNX2 double knockout mice revealed decreased anxiety-related behaviour, as assessed in the open field and elevated plus maze paradigms. By contrast, no major defects in learning, motor or sensory function were observed. Given the apparent absence of major NUMB dysfunction in LNX null animals, we performed a proteomic analysis to identify neuronal LNX-interacting proteins other than NUMB that might contribute to the anxiolytic phenotype observed. We identified and/or confirmed interactions of LNX1 and LNX2 with proteins known to have presynaptic and neuronal signalling functions, including the presynaptic active zone constituents ERC1, ERC2 and LIPRIN-αs (PPFIA1, PPFIA3), as well as the F-BAR domain proteins FCHSD2 (nervous wreck homologue) and SRGAP2. These and other novel LNX-interacting proteins identified are promising candidates to mediate LNX functions in the central nervous system, including their role in modulating anxiety-related behaviour.

Indexed as

LigandsAnimalsAnxietyCarrier ProteinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsMice, KnockoutNerve Tissue ProteinsNeuronsProteomicsUbiquitinUbiquitin-Protein LigasesCarrier ProteinsIntracellular Signaling Peptides and ProteinsLigandsLnx1 protein, mouseLnx2 protein, mouseMembrane ProteinsNerve Tissue ProteinsNumb protein, mouseUbiquitinUbiquitin-Protein LigasesAnxietyERC1/ERC2LIPRIN/PPFIALNX1LNX2NUMB

Identifiers

PMID27889896
OpenAlexW2555764512

What OpenQuestion holds

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Registered trials

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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.