Evidence map›Paper›PMID 36404134›Full record

ArticleAging cell2023

Large-scale genetic screens identify BET-1 as a cytoskeleton regulator promoting actin function and life span.

Gilberto Garcia, Raz Bar-Ziv, Maxim Averbukh, Nirmalya Dasgupta, Naibedya Dutta, Hanlin Zhang, Wudi Fan, Darius Moaddeli, C Kimberly Tsui, Toni Castro Torres and 7 more

Abstract read
In one paragraph

Article in Aging cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Alterations of actin in aging.Journal of cell science · 2026
    Review
  7. Distinct responses to non-autonomous UPRCommunications biology · 2025
    Article
  8. Form and function of actin impacts actin health and aging.bioRxiv : the preprint server for biology · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. 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

17 authors.

Gilberto GarciaLeonard Davis School of Gerontology, University of Southern California, Los Angeles, California, USA.
Raz Bar-ZivDepartment of Molecular & Cellular Biology, Howard Hughes Medical Institute, The University of California, Berkeley, Berkeley, California, USA.
Maxim AverbukhLeonard Davis School of Gerontology, University of Southern California, Los Angeles, California, USA.
Nirmalya DasguptaAging, Cancer and Immuno-oncology Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California, USA.ORCID 0000-0002-0289-5712
Naibedya DuttaLeonard Davis School of Gerontology, University of Southern California, Los Angeles, California, USA.
Hanlin ZhangDepartment of Molecular & Cellular Biology, Howard Hughes Medical Institute, The University of California, Berkeley, Berkeley, California, USA.
Wudi FanDepartment of Molecular & Cellular Biology, Howard Hughes Medical Institute, The University of California, Berkeley, Berkeley, California, USA.
Darius MoaddeliLeonard Davis School of Gerontology, University of Southern California, Los Angeles, California, USA.
C Kimberly TsuiDepartment of Molecular & Cellular Biology, Howard Hughes Medical Institute, The University of California, Berkeley, Berkeley, California, USA.
Toni Castro TorresLeonard Davis School of Gerontology, University of Southern California, Los Angeles, California, USA.
Athena AlcalaLeonard Davis School of Gerontology, University of Southern California, Los Angeles, California, USA.
Erica A MoehleDepartment of Molecular & Cellular Biology, Howard Hughes Medical Institute, The University of California, Berkeley, Berkeley, California, USA.
Sally HoangLeonard Davis School of Gerontology, University of Southern California, Los Angeles, California, USA.
Ophir ShalemDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Peter D AdamsAging, Cancer and Immuno-oncology Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California, USA.ORCID 0000-0002-0684-1770
Max A ThorwaldLeonard Davis School of Gerontology, University of Southern California, Los Angeles, California, USA.
Ryo Higuchi-SanabriaLeonard Davis School of Gerontology, University of Southern California, Los Angeles, California, USA.ORCID 0000-0001-8936-5812

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
USC Geroscience Training in the Biology of AgingT32AG052374 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Sean P CURRAN · 2016 to 2026
$5.3M
Direct and rapid control of proteins at scaleDP2GM137416 · NIGMS · CHILDREN'S HOSP OF PHILADELPHIA · PI SHALEM, OPHIR · 2019 to 2022
$2.8M
Cytoplasmic chromatin fragments in cell senescence - novel mechanisms and interventionsR01AG071861 · NIA · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI ADAMS, PETER D. · 2021 to 2025
$2.3M
More than just a load control: cytoskeletal form and function during agingR00AG065200 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI HIGUCHI-SANABRIA, RYO · 2021 to 2023
$747k
Dissecting the mechanisms that underlie mislocalization and aggregation of RNA binding proteins in neurodegenerative diseasesR03NS111447 · NINDS · CHILDREN'S HOSP OF PHILADELPHIA · PI SHALEM, OPHIR · 2019 to 2019
$352k
Systemic Regulation of ER ProteostasisF32AG069388 · NIA · UNIVERSITY OF CALIFORNIA BERKELEY · PI TSUI, CHUNG YIN KIMBERLY · 2021 to 2023
$210k
NIA NIH HHS F32 AG069388NIA NIH HHS R00 AG065200NIA NIH HHS R01 AG071861NIA NIH HHS T32 AG052374NIGMS NIH HHS DP2 GM137416NIH HHS P40 OD010440NINDS NIH HHS R03 NS111447
6 · The paper itself

Abstract

The actin cytoskeleton is a three-dimensional scaffold of proteins that is a regulatory, energyconsuming network with dynamic properties to shape the structure and function of the cell. Proper actin function is required for many cellular pathways, including cell division, autophagy, chaperone function, endocytosis, and exocytosis. Deterioration of these processes manifests during aging and exposure to stress, which is in part due to the breakdown of the actin cytoskeleton. However, the regulatory mechanisms involved in preservation of cytoskeletal form and function are not well-understood. Here, we performed a multipronged, cross-organismal screen combining a whole-genome CRISPR-Cas9 screen in human fibroblasts with in vivo Caenorhabditis elegans synthetic lethality screening. We identified the bromodomain protein, BET-1, as a key regulator of actin function and longevity. Overexpression of bet-1 preserves actin function at late age and promotes life span and healthspan in C. elegans. These beneficial effects are mediated through actin preservation by the transcriptional regulator function of BET-1. Together, our discovery assigns a key role for BET-1 in cytoskeletal health, highlighting regulatory cellular networks promoting cytoskeletal homeostasis.

Indexed as

Caenorhabditis elegans ProteinsLongevityActin CytoskeletonActinsAnimalsCaenorhabditis elegansCytoskeletonHumansActinsCaenorhabditis elegans ProteinsactinagingCRISPR

Identifiers

PMID36404134
PMCPMC9835578

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.