Tsukamoto T, Bogaki A, Okumoto K, Tateishi K, Fujiki Y, Shimozawa N, Suzuki Y, Kondo N, Osumi T
Department of Life Science, Himeji Institute of Technology, Kamigori, Hyogo, Japan.
Biochem Biophys Res Commun. 1997 Jan 13;230(2):402-6. doi: 10.1006/bbrc.1996.5971.
For the study of mechanism of peroxisome biogenesis, we attempted to isolate CHO cell mutants deficient in peroxisome biogenesis. We used as the parent strain a stable CHO transformant of rat PEX2 (formerly named peroxisome assembly factor-1) cDNA, to avoid unusually frequent isolation of Pex2 mutants. Among the three peroxisome-deficient mutants obtained, ZP102 was a new CHO mutant of complementation group 2, and was restored for peroxisome assembly by the transfection of human PEX5 (formerly called PXR1 or PTS1R) cDNA. This approach would facilitate the isolation of new complementation gorups of peroxisome-deficient CHO mutants and the identification of essential genes for peroxisome biogenesis.
为了研究过氧化物酶体生物发生的机制,我们试图分离出在过氧化物酶体生物发生方面存在缺陷的中国仓鼠卵巢(CHO)细胞突变体。我们使用大鼠PEX2(以前称为过氧化物酶体组装因子-1)cDNA的稳定CHO转化体作为亲本菌株,以避免异常频繁地分离出Pex2突变体。在获得的三个过氧化物酶体缺陷突变体中,ZP102是互补群2的一个新的CHO突变体,通过转染人PEX5(以前称为PXR1或PTS1R)cDNA可恢复其过氧化物酶体组装。这种方法将有助于分离过氧化物酶体缺陷的CHO突变体的新互补群,并鉴定过氧化物酶体生物发生的必需基因。