Evidence map›Paper›PMID 34277363›Full record

ArticleBiotechnology reports (Amsterdam, Netherlands)2021

A pooled CRISPR/AsCpf1 screen using paired gRNAs to induce genomic deletions in Chinese hamster ovary cells.

Valerie Schmieder, Neža Novak, Heena Dhiman, Ly Ngoc Nguyen, Evgenija Serafimova, Gerald Klanert, Martina Baumann, Helene Faustrup Kildegaard, Nicole Borth

Open access · goldAbstract read
In one paragraph

Article in Biotechnology reports (Amsterdam, Netherlands), 2021. 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
0.8field-weighted citation impact, top 29% 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, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. CRISPR Technologies in Chinese Hamster Ovary Cell Line Engineering.International journal of molecular sciences · 2023
    Review
  4. 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

9 authors at 3 institutions in 2 countries.

Valerie SchmiederDepartment of Biotechnology, BOKU University of Natural Resources and Life Sciences, Muthgasse 18, Vienna, Austria.
Neža NovakDepartment of Biotechnology, BOKU University of Natural Resources and Life Sciences, Muthgasse 18, Vienna, Austria.
Heena DhimanDepartment of Biotechnology, BOKU University of Natural Resources and Life Sciences, Muthgasse 18, Vienna, Austria.
Ly Ngoc NguyenDepartment of Biotechnology, BOKU University of Natural Resources and Life Sciences, Muthgasse 18, Vienna, Austria.
Evgenija SerafimovaDepartment of Biotechnology, BOKU University of Natural Resources and Life Sciences, Muthgasse 18, Vienna, Austria.
Gerald Klanertacib GmbH, Austrian Centre of Industrial Biotechnology, Muthgasse 11, Vienna, Austria.
Martina Baumannacib GmbH, Austrian Centre of Industrial Biotechnology, Muthgasse 11, Vienna, Austria.
Helene Faustrup KildegaardThe Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Building 220, Kemitorvet, Kgs. Lyngby, Denmark.
Nicole BorthDepartment of Biotechnology, BOKU University of Natural Resources and Life Sciences, Muthgasse 18, Vienna, Austria.
Austrian Centre of Industrial Biotechnology (Austria) · ATBOKU University · ATNovo Nordisk Foundation · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chinese hamster ovary (CHO) cells are the most widely used host for the expression of therapeutic proteins. Recently, significant progress has been made due to advances in genome sequence and annotation quality to unravel the black box CHO. Nevertheless, in many cases the link between genotype and phenotype in the context of suspension cultivated production cell lines is still not fully understood. While frameshift approaches targeting coding genes are frequently used, the non-coding regions of the genome have received less attention with respect to such functional annotation. Importantly, for non-coding regions frameshift knock-out strategies are not feasible. In this study, we developed a CRISPR-mediated screening approach that performs full deletions of genomic regions to enable the functional study of both the translated and untranslated genome. An

Indexed as

AsCpf1, Cpf1 from Acidaminococcus sp BV3L6Cas9, CRISPR-associated protein 9Chinese hamster ovary cellsCHO, Chinese hamster ovaryCpf1, CRISPR-associated protein in Prevotella and FrancisellaCPM, counts per million reads mappedCRISPR/AsCpf1CRISPR, Clustered Regularly Interspaced Short Palindromic RepeatsdCas9, deactivated Cas9DE, differentially expressedDOWN-TTS, downstream transcription termination siteDR, differentially representedEpoFc, Erythropoietin Fc fusion proteinEV, empty vectorFACS, fluorescence activated cell sortingFC, fold changeFDR, false discovery rateGenetic screengenomic deletiongRNA, guide RNAGS, glutamine synthetaselncRNA, long non-coding RNAncGene, non-coding geneNGS, next generation sequencingNTC, no template controloligo, oligonucleotidepaired gRNAsPAM, protospacer adjacent motifPCA, principal component analysispgRNA, paired gRNAQp, specific productivityRMCE, recombinase-mediated cassette exchangesgRNA, single guide RNATMM, trimmed mean of M valuesUP-TSS, upstream transcription start siteVCD, viable cell densityµ, growth rate

Identifiers

PMID34277363
PMCPMC8261548
OpenAlexW3176774265

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.