Evidence map›Paper›PMID 34999833›Full record

ArticleHuman molecular genetics2022

Abnormal activation of Yap/Taz contributes to the pathogenesis of tuberous sclerosis complex.

Bethany K Terry, Raehee Park, Seo-Hee Cho, Peter B Crino, Seonhee Kim

Open access · greenAbstract read
In one paragraph

Article in Human molecular genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

5 authors at 3 institutions in 1 country.

Bethany K TerryDepartment of Neural Sciences, Lewis Katz School of Medicine, Shriners Hospitals Pediatrics Research Center, Temple University, Philadelphia, PA 19140, USA.ORCID 0000-0001-7205-4516
Raehee ParkDepartment of Neural Sciences, Lewis Katz School of Medicine, Shriners Hospitals Pediatrics Research Center, Temple University, Philadelphia, PA 19140, USA.
Seo-Hee ChoDepartment of Medicine, Sidney Kimmel Medical College, Center for Translational Medicine, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Peter B CrinoDepartment of Neurology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Seonhee KimDepartment of Neural Sciences, Lewis Katz School of Medicine, Shriners Hospitals Pediatrics Research Center, Temple University, Philadelphia, PA 19140, USA.ORCID 0000-0003-4559-6381
University of the Sciences · USThomas Jefferson University · USUniversity of Maryland, Baltimore · US

Funding

Antagonistic interaction of polarity complex proteins in cortical developmentR01NS104038 · NINDS · TEMPLE UNIV OF THE COMMONWEALTH · PI KIM, SEONHEE · 2019 to 2022
$1.4M
Antagonistic interaction of polarity complex proteins in cortical developmentR56NS104038 · NINDS · TEMPLE UNIV OF THE COMMONWEALTH · PI KIM, SEONHEE · 2018 to 2018
$390k
NINDS NIH HHS R01 NS104038NINDS NIH HHS R56 NS104038
6 · The paper itself

Abstract

The multi-systemic genetic disorder tuberous sclerosis complex (TSC) impacts multiple neurodevelopmental processes including neuronal morphogenesis, neuronal migration, myelination and gliogenesis. These alterations contribute to the development of cerebral cortex abnormalities and malformations. Although TSC is caused by mTORC1 hyperactivation, cognitive and behavioral impairments are not improved through mTORC1 targeting, making the study of the downstream effectors of this complex important for understanding the mechanisms underlying TSC. As mTORC1 has been shown to promote the activity of the transcriptional co-activator Yap, we hypothesized that altered Yap/Taz signaling contributes to the pathogenesis of TSC. We first observed that the levels of Yap/Taz are increased in human cortical tuber samples and in embryonic cortices of Tsc2 conditional knockout (cKO) mice. Next, to determine how abnormal upregulation of Yap/Taz impacts the neuropathology of TSC, we deleted Yap/Taz in Tsc2 cKO mice. Importantly, Yap/Taz/Tsc2 triple conditional knockout (tcKO) animals show reduced cortical thickness and cortical neuron cell size, despite the persistence of high mTORC1 activity, suggesting that Yap/Taz play a downstream role in cytomegaly. Furthermore, Yap/Taz/Tsc2 tcKO significantly restored cortical and hippocampal lamination defects and reduced hippocampal heterotopia formation. Finally, the loss of Yap/Taz increased the distribution of myelin basic protein in Tsc2 cKO animals, consistent with an improvement in myelination. Overall, our results indicate that targeting Yap/Taz lessens the severity of neuropathology in a TSC animal model. This study is the first to implicate Yap/Taz as contributors to cortical pathogenesis in TSC and therefore as potential novel targets in the treatment of this disorder.

Indexed as

Adaptor Proteins, Signal TransducingTuberous SclerosisYAP-Signaling ProteinsAnimalsMechanistic Target of Rapamycin Complex 1MiceNeuronsTranscription FactorsTuberous Sclerosis Complex 1 ProteinAdaptor Proteins, Signal TransducingMechanistic Target of Rapamycin Complex 1Transcription FactorsTuberous Sclerosis Complex 1 ProteinWwtr1 protein, mouseYap1 protein, mouseYAP-Signaling Proteins

Identifiers

PMID34999833
PMCPMC9239747
OpenAlexW4206384005

What Socratic holds

Textmetadata
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 Socratic graph.