Evidence map›Paper›PMID 37280197›Full record

ArticleNature communications2023

LIS1 RNA-binding orchestrates the mechanosensitive properties of embryonic stem cells in AGO2-dependent and independent ways.

Aditya Kshirsagar, Svetlana Maslov Doroshev, Anna Gorelik, Tsviya Olender, Tamar Sapir, Daisuke Tsuboi, Irit Rosenhek-Goldian, Sergey Malitsky, Maxim Itkin, Amir Argoetti and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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

16 authors at 3 institutions in 2 countries.

Aditya KshirsagarDepartments of Molecular Genetics and Molecular Neuroscience, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0001-8926-9353
Svetlana Maslov DoroshevDepartments of Molecular Genetics and Molecular Neuroscience, Weizmann Institute of Science, Rehovot, Israel.
Anna GorelikDepartments of Molecular Genetics and Molecular Neuroscience, Weizmann Institute of Science, Rehovot, Israel.
Tsviya OlenderDepartments of Molecular Genetics and Molecular Neuroscience, Weizmann Institute of Science, Rehovot, Israel.
Tamar SapirDepartments of Molecular Genetics and Molecular Neuroscience, Weizmann Institute of Science, Rehovot, Israel.
Daisuke TsuboiInternational Center for Brain Science, Fujita Health University, Toyoake, Japan.
Irit Rosenhek-GoldianDepartment of Chemical Research Support, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0002-4878-5359
Sergey MalitskyDepartment of Life Sciences Core Facilities, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0003-4619-7219
Maxim ItkinDepartment of Life Sciences Core Facilities, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0003-1348-2814
Amir ArgoettiFaculty of Biology, Technion-Israel Institute of Technology, Haifa, Israel.
Yael Mandel-GutfreundFaculty of Biology, Technion-Israel Institute of Technology, Haifa, Israel.
Sidney R CohenDepartment of Chemical Research Support, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0003-4255-3351
Jacob H HannaDepartments of Molecular Genetics and Molecular Neuroscience, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0003-2042-9974
Igor UlitskyDepartment of Immunology and Regenerative Biology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0003-0555-6561
Kozo KaibuchiInternational Center for Brain Science, Fujita Health University, Toyoake, Japan.
Orly ReinerDepartments of Molecular Genetics and Molecular Neuroscience, Weizmann Institute of Science, Rehovot, Israel. orly.reiner@weizmann.ac.il.ORCID 0000-0001-7560-9599
Weizmann Institute of Science · ILFujita Health University · JPTechnion – Israel Institute of Technology · IL

Funding

CIHR
6 · The paper itself

Abstract

Lissencephaly-1 (LIS1) is associated with neurodevelopmental diseases and is known to regulate the molecular motor cytoplasmic dynein activity. Here we show that LIS1 is essential for the viability of mouse embryonic stem cells (mESCs), and it governs the physical properties of these cells. LIS1 dosage substantially affects gene expression, and we uncovered an unexpected interaction of LIS1 with RNA and RNA-binding proteins, most prominently the Argonaute complex. We demonstrate that LIS1 overexpression partially rescued the extracellular matrix (ECM) expression and mechanosensitive genes conferring stiffness to Argonaute null mESCs. Collectively, our data transforms the current perspective on the roles of LIS1 in post-transcriptional regulation underlying development and mechanosensitive processes.

Indexed as

1-Alkyl-2-acetylglycerophosphocholine EsteraseArgonaute ProteinsEmbryonic Stem CellsMicrotubule-Associated ProteinsAnimalsBlastocystCell SurvivalEmbryo, MammalianMicePluripotent Stem CellsProtein Interaction Maps1-Alkyl-2-acetylglycerophosphocholine EsteraseAgo2 protein, mouseArgonaute ProteinsMicrotubule-Associated ProteinsPafah1b1 protein, mouse

Identifiers

PMID37280197
PMCPMC10244377
OpenAlexW4379598154

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.