Evidence map›Paper›PMID 41270742›Full record

ArticleDevelopmental cell2026

A microscopy-based CRISPR screening platform enables organellar functional genomics and illuminates ciliary biology.

Jingbo Sun, Irem Sude Atiş, Stéfany L L Empke, Mustafa K Khokha, David K Breslow

Abstract read
In one paragraph

Article in Developmental cell, 2026. 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
–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

1 citing paper in PubMed.

  1. Review
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.

Jingbo SunDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, USA.
Irem Sude AtişDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, USA.
Stéfany L L EmpkeDepartment of Pediatrics and Department of Genetics, Yale University School of Medicine, New Haven, CT, USA; Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
Mustafa K KhokhaDepartment of Pediatrics and Department of Genetics, Yale University School of Medicine, New Haven, CT, USA; Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
David K BreslowDepartment of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT, USA; Wu Tsai Institute, Yale University, New Haven, CT, USA. Electronic address: david.breslow@yale.edu.

Funding

A system approach to the analysis of Heterotaxy Candidate GenesR01HD102186 · NICHD · YALE UNIVERSITY · PI KHOKHA, MUSTAFA K · 2020 to 2024
$3.1M
Mechanisms of Primary Cilium Assembly and DisassemblyR35GM137956 · NIGMS · YALE UNIVERSITY · PI David King Breslow · 2020 to 2026
$3.1M
High Performance Computing Instrumentation for the Yale Center for Genome AnalysisS10OD030363 · OD · YALE UNIVERSITY · PI MANE, SHRIKANT M · 2022 to 2022
$1.2M
High Resolution Tandem Mass Spectrometer to Meet Growing Demand for Proteomics at YaleS10OD023651 · OD · YALE UNIVERSITY · PI LAM, TUKIET T · 2018 to 2018
$572k
6500 QTrap Mass Spectrometer for Yale UniversityS10OD018034 · OD · YALE UNIVERSITY · PI MANE, SHRIKANT M · 2014 to 2014
$514k
NICHD NIH HHS R01 HD102186NIGMS NIH HHS R35 GM137956NIH HHS S10 OD018034NIH HHS S10 OD023651NIH HHS S10 OD030363
6 · The paper itself

Abstract

Microscopy offers an indispensable technique for visualizing biological processes and for defining cytological abnormalities characteristic of disease. However, combining microscopy with the power of pooled CRISPR screening presents considerable technical challenges, hindering application of systematic genetic analysis to imaging-defined phenotypes. Here, we establish a fluorescence microscopy-based CRISPR screening platform that combines ease of implementation with flexible analysis of live-cell or antibody-based molecular markers, including post-translational modifications. Applying this methodology, we systematically identify regulators of primary cilium structure and function in human cells through targeted and genome-wide screens. We further show that integration of screens focused on distinct ciliary phenotypes yields multi-dimensional profiles that delineate precise gene functions. Among the identified hits, TZMP1 (SMIM27) encodes a microprotein at the ciliary transition zone that is required for ciliogenesis in human cells and for ciliary function in Xenopus embryos. More broadly, our approach provides a technological and conceptual strategy for microscopy-based functional genomics.

Indexed as

CiliaClustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsGenomicsAnimalsHumansMicroscopy, FluorescenceXenopusaxonemeciliaciliopathyCRISPR screenfunctional genomicsmicroproteinoptical screeningpolyglutamylationtransition zone

Identifiers

PMID41270742
PMCPMC12662653

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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.