Evidence map›Paper›PMID 27163549›Full record

ArticleExperimental neurology2016

Motor phenotypes and molecular networks associated with germline deficiency of Ciz1.

Jianfeng Xiao, Satya R Vemula, Yi Xue, Mohammad M Khan, Korah P Kuruvilla, Esther M Marquez-Lona, Madison R Cobb, Mark S LeDoux

Abstract read
In one paragraph

Article in Experimental neurology, 2016. 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
3.6field-weighted citation impact, top 7% 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, 15 citations in OpenAlex.

  1. Article
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  4. DNA double-strand breaks: a potential therapeutic target for neurodegenerative diseases.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2019
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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

8 authors at 1 institution in 1 country.

Jianfeng XiaoDepartments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Satya R VemulaDepartments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Yi XueDepartments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Mohammad M KhanDepartments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Korah P KuruvillaDepartments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Esther M Marquez-LonaDepartments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Madison R CobbDepartments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.
Mark S LeDouxDepartments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA. Electronic address: mledoux@uthsc.edu.
University of Tennessee Health Science Center · US

Funding

Genetics and Biology of CIZ1 in Cervical DystoniaR01NS082296 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI LEDOUX, MARK S · 2013 to 2016
$1.3M
The Role of THAP1 in DystoniaR01NS069936 · NINDS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI LEDOUX, MARK S · 2010 to 2013
$1.3M
The Role of UBTF in Undiagnosed Neurodevelopmental DisordersR21GM118962 · NIGMS · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI HORI, RODERICK T · 2016 to 2017
$456k
NIGMS NIH HHS R21 GM118962NINDS NIH HHS R01 NS069936NINDS NIH HHS R01 NS082296
6 · The paper itself

Abstract

A missense mutation in CIZ1 (c.790A>G, p.S264G) was linked to autosomal dominant cervical dystonia in a large multiplex Caucasian pedigree (OMIM614860, DYT23). CIZ1 is a p21((Cip1/Waf1)) -interacting zinc finger protein, widely expressed in neural and extra-neural tissues, and plays a role in DNA synthesis at the G1/S cell-cycle checkpoint. The role of CIZ1 in the nervous system and relative contributions of gain- or loss- of function to the pathogenesis of CIZ1-associated dystonia remain indefinite. Using relative quantitative reverse transcriptase-PCR, cerebellum showed the highest expression levels of Ciz1 in adult mouse brain, over two fold higher than liver, and higher than striatum, midbrain and cerebral cortex. Overall, neural expression of Ciz1 increased with postnatal age. A Ciz1 gene-trap knock-out (KO) mouse model (Ciz1(-/-)) was generated to examine the functional role(s) of CIZ1 in the sensorimotor nervous system and contributions of CIZ1 to cell-cycle control in the mammalian brain. Ciz1 transcripts were absent in Ciz1(-/-) mice and reduced by approximately 50% in Ciz1(+/-) mice. Ciz1(-/-) mice were fertile but smaller than wild-type (WT) littermates. Ciz1(-/-) mice did not manifest dystonia, but exhibited mild motoric abnormalities on balance, open-field activity, and gait. To determine the effects of germline KO of Ciz1 on whole-genome gene expression in adult brain, total RNA from mouse cerebellum was harvested from 6 10-month old Ciz1(-/-) mice and 6 age- and gender- matched WT littermates for whole-genome gene expression analysis. Based on whole-genome gene-expression analyses, genes involved in cellular movement, cell development, cellular growth, cellular morphology and cell-to-cell signaling and interaction were up-regulated in Ciz1(-/-) mice. The top up-regulated pathways were metabolic and cytokine-cytokine receptor interactions. Down-regulated genes were involved in cell cycle, cellular development, cell death and survival, gene expression and cell morphology. Down-regulated networks included those related to metabolism, focal adhesion, neuroactive ligand-receptor interaction, and MAPK signaling. Based on pathway analyses, transcription factor 7-like 2 (TCF7L2), a member of the Wnt/β-catenin signaling pathway, was a major hub for down-regulated genes, whereas NF-κB was a major hub for up-regulated genes. In aggregate, these data suggest that CIZ1 may be involved in the post-mitotic differentiation of neurons in response to external signals and changes in gene expression may compensate, in part, for CIZ1 deficiency in our Ciz1(-/-) mouse model. Although CIZ1 deficiency was associated with mild motor abnormalities, germline loss of Ciz1 was not associated with dystonia on the C57BL/6J background.

Indexed as

Movement DisordersAge FactorsAnimalsAnimals, NewbornBrainDisease Models, AnimalExploratory BehaviorFemaleGaitGene Regulatory NetworksGenomeMaleMiceMice, TransgenicMuscle StrengthNuclear ProteinsCiz1 protein, mouseNuclear ProteinsCell cycleCerebellumCIZ1DystoniaGene expressionKnock-out mouse

Identifiers

PMID27163549
PMCPMC4992595
OpenAlexW2363218275

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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.