{"title":"In pursuit of a minimal CHO genome: Establishment of large-scale genome deletions","authors":"Tobias Jerabek , Linus Weiß , Hannah Fahrion , Nikolas Zeh , Nadja Raab , Benjamin Lindner , Simon Fischer , Kerstin Otte","doi":"10.1016/j.nbt.2023.12.007","DOIUrl":null,"url":null,"abstract":"<div><p>Chinese hamster ovary (CHO) cells are the most commonly used mammalian cell line for the production of complex therapeutic glycoproteins. As CHO cells have evolved as part of a multicellular organism, they harbor many cellular functions irrelevant for their application as production hosts in industrial bioprocesses. Consequently, CHO cells have been the target for numerous genetic engineering efforts in the past, but a tailored host cell chassis holistically optimized for its specific task in a bioreactor is still missing. While the concept of genome reduction has already been successfully applied to bacterial production cells, attempts to create higher eukaryotic production hosts exhibiting reduced genomes have not been reported yet. Here, we present the establishment and application of a large-scale genome deletion strategy for targeted excision of large genomic regions in CHO cells. We demonstrate the feasibility of genome reduction in CHO cells using optimized CRISPR/Cas9 based experimental protocols targeting large non-essential genomic regions with high efficiency. Achieved genome deletions of non-essential genetic regions did not introduce negative effects on bioprocess relevant parameters, although we conducted the largest reported genomic excision of 864 kilobase pairs in CHO cells so far. The concept presented serves as a directive to accelerate the development of a significantly genome-reduced CHO host cell chassis paving the way for a next generation of CHO cell factories.</p></div>","PeriodicalId":19190,"journal":{"name":"New biotechnology","volume":"79 ","pages":"Pages 100-110"},"PeriodicalIF":4.5000,"publicationDate":"2023-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1871678423000754/pdfft?md5=61771dcaec320ae3b670e1e43b896980&pid=1-s2.0-S1871678423000754-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New biotechnology","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1871678423000754","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
Chinese hamster ovary (CHO) cells are the most commonly used mammalian cell line for the production of complex therapeutic glycoproteins. As CHO cells have evolved as part of a multicellular organism, they harbor many cellular functions irrelevant for their application as production hosts in industrial bioprocesses. Consequently, CHO cells have been the target for numerous genetic engineering efforts in the past, but a tailored host cell chassis holistically optimized for its specific task in a bioreactor is still missing. While the concept of genome reduction has already been successfully applied to bacterial production cells, attempts to create higher eukaryotic production hosts exhibiting reduced genomes have not been reported yet. Here, we present the establishment and application of a large-scale genome deletion strategy for targeted excision of large genomic regions in CHO cells. We demonstrate the feasibility of genome reduction in CHO cells using optimized CRISPR/Cas9 based experimental protocols targeting large non-essential genomic regions with high efficiency. Achieved genome deletions of non-essential genetic regions did not introduce negative effects on bioprocess relevant parameters, although we conducted the largest reported genomic excision of 864 kilobase pairs in CHO cells so far. The concept presented serves as a directive to accelerate the development of a significantly genome-reduced CHO host cell chassis paving the way for a next generation of CHO cell factories.
中国仓鼠卵巢(CHO)细胞是生产复杂治疗糖蛋白最常用的哺乳动物细胞系。由于 CHO 细胞是作为多细胞生物体的一部分进化而来的,因此它们具有许多与其作为工业生物工艺中的生产宿主无关的细胞功能。因此,CHO 细胞在过去一直是众多基因工程研究的目标,但目前仍缺少一种针对其在生物反应器中的特定任务进行整体优化的定制宿主细胞底盘。虽然基因组缩减的概念已经成功应用于细菌生产细胞,但试图创造出基因组缩减的高等真核生产宿主的尝试尚未见报道。在这里,我们介绍了一种大规模基因组删除策略的建立和应用,该策略可在 CHO 细胞中定向切除大的基因组区域。我们利用基于 CRISPR/Cas9 的优化实验方案,针对大的非必要基因组区域,高效率地证明了在 CHO 细胞中减少基因组的可行性。尽管我们在 CHO 细胞中进行了迄今为止最大的基因组切除(864 千碱基对),但所实现的非必要基因区域的基因组删除并未对生物工艺相关参数产生负面影响。我们提出的这一概念为加速开发基因组显著减少的 CHO 宿主细胞底盘提供了指导,为下一代 CHO 细胞工厂铺平了道路。
期刊介绍:
New Biotechnology is the official journal of the European Federation of Biotechnology (EFB) and is published bimonthly. It covers both the science of biotechnology and its surrounding political, business and financial milieu. The journal publishes peer-reviewed basic research papers, authoritative reviews, feature articles and opinions in all areas of biotechnology. It reflects the full diversity of current biotechnology science, particularly those advances in research and practice that open opportunities for exploitation of knowledge, commercially or otherwise, together with news, discussion and comment on broader issues of general interest and concern. The outlook is fully international.
The scope of the journal includes the research, industrial and commercial aspects of biotechnology, in areas such as: Healthcare and Pharmaceuticals; Food and Agriculture; Biofuels; Genetic Engineering and Molecular Biology; Genomics and Synthetic Biology; Nanotechnology; Environment and Biodiversity; Biocatalysis; Bioremediation; Process engineering.