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来自过氧化物酶体缺陷型中国仓鼠卵巢(CHO)细胞突变体的经验教训。

Lessons from peroxisome-deficient Chinese hamster ovary (CHO) cell mutants.

作者信息

Fujiki Yukio, Okumoto Kanji, Kinoshita Naohiko, Ghaedi Kamran

机构信息

Department of Biology, Faculty of Sciences, Kyushu University Graduate School, 6-10-1 Hakozaki, Fukuoka 812-8581, Japan.

出版信息

Biochim Biophys Acta. 2006 Dec;1763(12):1374-81. doi: 10.1016/j.bbamcr.2006.09.012. Epub 2006 Sep 14.

Abstract

Cells with a genetic defect affecting a biological activity and/or a cell phenotype are generally called "cell mutants" and are a highly useful tool in genetic, biochemical, as well as cell biological research. To investigate peroxisome biogenesis and human peroxisome biogenesis disorders, more than a dozen complementation groups of Chinese hamster ovary (CHO) cell mutants defective in peroxisome assembly have been successfully isolated and established as a model system. Moreover, successful PEX gene cloning studies by taking advantage of rapid functional complementation assay of CHO cell mutants invaluably contributed to the accomplishment of isolation of pathogenic genes responsible for peroxisome biogenesis diseases. Molecular mechanisms of peroxisome assembly are currently investigated by making use of such mammalian cell mutants.

摘要

具有影响生物活性和/或细胞表型的遗传缺陷的细胞通常被称为“细胞突变体”,是遗传、生化以及细胞生物学研究中非常有用的工具。为了研究过氧化物酶体生物发生和人类过氧化物酶体生物发生障碍,已经成功分离出十多个在过氧化物酶体组装方面存在缺陷的中国仓鼠卵巢(CHO)细胞突变体互补组,并将其建立为一个模型系统。此外,利用CHO细胞突变体的快速功能互补分析进行的PEX基因克隆研究,为成功分离导致过氧化物酶体生物发生疾病的致病基因做出了不可估量的贡献。目前正在利用此类哺乳动物细胞突变体研究过氧化物酶体组装的分子机制。

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