Thieringer R, Raetz C R
Merck Research Laboratories, Rahway, New Jersey 07065.
J Biol Chem. 1993 Jun 15;268(17):12631-6.
Chinese hamster ovary (CHO) mutant cells deficient in peroxisome biogenesis regain peroxisomes after transfection with a cDNA coding for peroxisome assembly factor (PAF)-1 from rat liver. Reconstitution of the transfected mutant cells with wild-type cytoplasm was not required, demonstrating that expression of the PAF-1 gene alone was sufficient for the restoration of peroxisome biogenesis. Plasmalogen biosynthesis in the transfected mutants was also restored to approximately wild-type levels. The nucleotide sequence of the cDNA encoding the open reading frame for PAF-1 from CHO-K1 cells was determined. This allowed us to identify point mutations of PAF-1 in two peroxisomal mutant cell lines. The mutation in ZR-78 cells changed a cysteine to a tyrosine codon in a region located at the carboxyl terminus of the protein, which resembles the zinc finger motif of DNA-binding proteins. A point mutation in the PAF-1 gene of ZR-82 leads to premature termination.
缺乏过氧化物酶体生物发生的中国仓鼠卵巢(CHO)突变细胞在转染了编码大鼠肝脏过氧化物酶体组装因子(PAF)-1的cDNA后重新获得了过氧化物酶体。不需要用野生型细胞质重建转染的突变细胞,这表明单独PAF-1基因的表达足以恢复过氧化物酶体生物发生。转染突变体中的缩醛磷脂生物合成也恢复到了大约野生型水平。确定了编码CHO-K1细胞PAF-1开放阅读框的cDNA的核苷酸序列。这使我们能够鉴定两种过氧化物酶体突变细胞系中PAF-1的点突变。ZR-78细胞中的突变将蛋白质羧基末端区域的一个半胱氨酸密码子变为酪氨酸密码子,该区域类似于DNA结合蛋白的锌指基序。ZR-82的PAF-1基因中的一个点突变导致提前终止。