Evidence map›Paper›PMID 33147445›Full record

ArticleCell2021

Identification of Required Host Factors for SARS-CoV-2 Infection in Human Cells.

Zharko Daniloski, Tristan X Jordan, Hans-Hermann Wessels, Daisy A Hoagland, Silva Kasela, Mateusz Legut, Silas Maniatis, Eleni P Mimitou, Lu Lu, Evan Geller and 7 more

Open access · greenAbstract read
In one paragraph

Article in Cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 413 papers.

0numbers the graph read from it
0cells of the map it votes in
413citing papers in PubMed
12.8field-weighted citation impact, top 1% 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

413 citing papers in PubMed, 634 citations in OpenAlex.

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353 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 1 country.

Zharko DaniloskiNew York Genome Center, New York, NY, USA; Department of Biology, New York University, New York, NY, USA.
Tristan X JordanDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Hans-Hermann WesselsNew York Genome Center, New York, NY, USA; Department of Biology, New York University, New York, NY, USA.
Daisy A HoaglandDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Silva KaselaNew York Genome Center, New York, NY, USA; Department of Systems Biology, Columbia University, New York, NY, USA.
Mateusz LegutNew York Genome Center, New York, NY, USA; Department of Biology, New York University, New York, NY, USA.
Silas ManiatisNew York Genome Center, New York, NY, USA.
Eleni P MimitouTechnology Innovation Lab, New York Genome Center, New York, NY, USA.
Lu LuNew York Genome Center, New York, NY, USA; Department of Biology, New York University, New York, NY, USA.
Evan GellerNew York Genome Center, New York, NY, USA; Department of Biology, New York University, New York, NY, USA.
Oded DanzigerDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Brad R RosenbergDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Hemali PhatnaniNew York Genome Center, New York, NY, USA; Department of Neurology, Columbia University Irving Medical Center, New York, NY, USA.
Peter SmibertTechnology Innovation Lab, New York Genome Center, New York, NY, USA.
Tuuli LappalainenNew York Genome Center, New York, NY, USA; Department of Systems Biology, Columbia University, New York, NY, USA.
Benjamin R tenOeverDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Electronic address: benjamin.tenoever@mssm.edu.
Neville E SanjanaNew York Genome Center, New York, NY, USA; Department of Biology, New York University, New York, NY, USA. Electronic address: neville@sanjanalab.org.
New York Genome Center · USIcahn School of Medicine at Mount Sinai · USNew York University · USColumbia University · US

Funding

Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
New York Center for Collaborative Research In Common Disease Genomics: Genome Aggregation and Joint Variant Calling for CCDG Freeze2UM1HG008901 · NHGRI · NEW YORK GENOME CENTER · PI MANIATIS, THOMAS P, WIGLER, MICHAEL H · 2016 to 2020
$56.6M
Statistical models for fine-mapping and interpretation of schizophrenia-associated lociR01MH106842 · NIMH · NEW YORK GENOME CENTER · PI BUSSEMAKER, HARMEN J, LAPPALAINEN, TUULI · 2015 to 2024
$5.0M
Predicting the functional impact of non-coding mutations using patient-specific gene regulatory networksR01CA218668 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI EKTA KHURANA, Neville Sanjana · 2018 to 2026
$4.7M
In situ functional genomics to understand transcriptional regulationDP2HG010099 · NHGRI · NEW YORK GENOME CENTER · PI SANJANA, NEVILLE · 2017 to 2022
$4.4M
The biology of the nuclear export protein in influenza A virus replicationR01AI123155 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI TENOEVER, BENJAMIN R. · 2017 to 2020
$2.4M
Integration of omics data to improve interpretation of genetic risk variants in lung diseaseR01HL142028 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BARR, R GRAHAM, LAPPALAINEN, TUULI · 2018 to 2019
$790k
NCATS NIH HHS UL1 TR001873NCI NIH HHS R01 CA218668NHGRI NIH HHS DP2 HG010099NHGRI NIH HHS UM1 HG008901NHLBI NIH HHS R01 HL142028NIAID NIH HHS R01 AI123155NIMH NIH HHS R01 MH106842
6 · The paper itself

Abstract

To better understand host-virus genetic dependencies and find potential therapeutic targets for COVID-19, we performed a genome-scale CRISPR loss-of-function screen to identify host factors required for SARS-CoV-2 viral infection of human alveolar epithelial cells. Top-ranked genes cluster into distinct pathways, including the vacuolar ATPase proton pump, Retromer, and Commander complexes. We validate these gene targets using several orthogonal methods such as CRISPR knockout, RNA interference knockdown, and small-molecule inhibitors. Using single-cell RNA-sequencing, we identify shared transcriptional changes in cholesterol biosynthesis upon loss of top-ranked genes. In addition, given the key role of the ACE2 receptor in the early stages of viral entry, we show that loss of RAB7A reduces viral entry by sequestering the ACE2 receptor inside cells. Overall, this work provides a genome-scale, quantitative resource of the impact of the loss of each host gene on fitness/response to viral infection.

Indexed as

Host-Pathogen InteractionsA549 CellsAlveolar Epithelial CellsAngiotensin-Converting Enzyme 2Biosynthetic PathwaysCholesterolClustered Regularly Interspaced Short Palindromic RepeatsCOVID-19EndosomesGene Expression ProfilingGene Knockdown TechniquesGene Knockout TechniquesGenome-Wide Association StudyHumansrab7 GTP-Binding Proteinsrab GTP-Binding ProteinsACE2 protein, humanAngiotensin-Converting Enzyme 2Cholesterolrab7 GTP-Binding Proteinsrab GTP-Binding ProteinsCas9cholesterolCOVID-19CRISPRECCITE-seqendosomegenome-wide screenhuman lungloss of functionSARS-CoV-2

Identifiers

PMID33147445
PMCPMC7584921
OpenAlexW3093900830

What OpenQuestion 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 OpenQuestion graph.