Literature DB >> 29762913

An Online Compendium of CHO RNA-Seq Data Allows Identification of CHO Cell Line-Specific Transcriptomic Signatures.

Ankita Singh1,2, Helene F Kildegaard1, Mikael R Andersen2.   

Abstract

Chinese hamster ovary (CHO) cell lines can fold, assemble, and modify proteins post-translationally to produce human-like proteins; as a consequence, it is the single most common expression systems for industrial production of recombinant therapeutic proteins. A thorough knowledge of cultivation conditions of different CHO cell lines has been developed over the last decade, but comprehending gene or pathway-specific distinctions between CHO cell lines at transcriptome level remains a challenge. To address these challenges, a compendium of 23 RNA-Seq studies from public and in-house data on CHO cell lines, i.e., CHO-S, CHO-K1, and DG44 is compiled. Significantly differentially expressed (DE) genes particularly related to subcellular structure and macromolecular categories are used to identify differences between the cell lines. A R-based web application is developed specifically for CHO cell lines to further visualize expression values across different cell lines, and make available the normalized full CHO data set graphically as a CHO research community resource. This study quantitatively categorizes CHO cell lines based on patterns at transcriptomic level and detects gene and pathway specific key distinctions among sibling cell lines. Studies such as this can be used to select desired characteristics across various CHO cell lines. Furthermore, the availability of the data as an internet-based application can be applied to broad range of CHO engineering applications.
© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  CHO cells; CHO gene expression visualization application; bioinformatics; differential expression analysis; gene expression; omics; transcriptomics

Mesh:

Substances:

Year:  2018        PMID: 29762913     DOI: 10.1002/biot.201800070

Source DB:  PubMed          Journal:  Biotechnol J        ISSN: 1860-6768            Impact factor:   4.677


  9 in total

1.  Proteogenomic Annotation of Chinese Hamsters Reveals Extensive Novel Translation Events and Endogenous Retroviral Elements.

Authors:  Shangzhong Li; Seong Won Cha; Kelly Heffner; Deniz Baycin Hizal; Michael A Bowen; Raghothama Chaerkady; Robert N Cole; Vijay Tejwani; Prashant Kaushik; Michael Henry; Paula Meleady; Susan T Sharfstein; Michael J Betenbaugh; Vineet Bafna; Nathan E Lewis
Journal:  J Proteome Res       Date:  2019-05-08       Impact factor: 4.466

2.  Engineering death resistance in CHO cells for improved perfusion culture.

Authors:  Michael A MacDonald; Matthias Nöbel; Verónica S Martínez; Kym Baker; Evan Shave; Peter P Gray; Stephen Mahler; Trent Munro; Lars K Nielsen; Esteban Marcellin
Journal:  MAbs       Date:  2022 Jan-Dec       Impact factor: 6.440

3.  A cross-species whole genome siRNA screen in suspension-cultured Chinese hamster ovary cells identifies novel engineering targets.

Authors:  Gerald Klanert; Daniel J Fernandez; Marcus Weinguny; Peter Eisenhut; Eugen Bühler; Michael Melcher; Steven A Titus; Andreas B Diendorfer; Elisabeth Gludovacz; Vaibhav Jadhav; Su Xiao; Beate Stern; Madhu Lal; Joseph Shiloach; Nicole Borth
Journal:  Sci Rep       Date:  2019-06-18       Impact factor: 4.996

4.  Modeling apoptosis resistance in CHO cells with CRISPR-mediated knockouts of Bak1, Bax, and Bok.

Authors:  Michael A MacDonald; Craig Barry; Teddy Groves; Verónica S Martínez; Peter P Gray; Kym Baker; Evan Shave; Stephen Mahler; Trent Munro; Esteban Marcellin; Lars K Nielsen
Journal:  Biotechnol Bioeng       Date:  2022-03-06       Impact factor: 4.395

5.  A proteomics approach to decipher a sticky CHO situation.

Authors:  Swetha Kumar; Amit Kumar; Steven Huhn; Lauren DeVine; Robert Cole; Zhimei Du; Michael Betenbaugh
Journal:  Biotechnol Bioeng       Date:  2022-05-25       Impact factor: 4.395

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

Authors:  Valerie Schmieder; Neža Novak; Heena Dhiman; Ly Ngoc Nguyen; Evgenija Serafimova; Gerald Klanert; Martina Baumann; Helene Faustrup Kildegaard; Nicole Borth
Journal:  Biotechnol Rep (Amst)       Date:  2021-06-20

7.  A Chinese hamster transcription start site atlas that enables targeted editing of CHO cells.

Authors:  Isaac Shamie; Sascha H Duttke; Karen J la Cour Karottki; Claudia Z Han; Anders H Hansen; Hooman Hefzi; Kai Xiong; Shangzhong Li; Samuel J Roth; Jenhan Tao; Gyun Min Lee; Christopher K Glass; Helene Faustrup Kildegaard; Christopher Benner; Nathan E Lewis
Journal:  NAR Genom Bioinform       Date:  2021-07-13

8.  Defining lncRNAs Correlated with CHO Cell Growth and IgG Productivity by RNA-Seq.

Authors:  Davide Vito; Jens Christian Eriksen; Christian Skjødt; Dietmar Weilguny; Søren K Rasmussen; C Mark Smales
Journal:  iScience       Date:  2019-12-18

9.  Random epigenetic modulation of CHO cells by repeated knockdown of DNA methyltransferases increases population diversity and enables sorting of cells with higher production capacities.

Authors:  Marcus Weinguny; Peter Eisenhut; Gerald Klanert; Nikolaus Virgolini; Nicolas Marx; Andreas Jonsson; Daniel Ivansson; Ann Lövgren; Nicole Borth
Journal:  Biotechnol Bioeng       Date:  2020-07-24       Impact factor: 4.395

  9 in total

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