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过氧化物酶体组装因子1:过氧化物酶体缺陷的中国仓鼠卵巢细胞突变体中的无义突变及缺失分析。

Peroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis.

作者信息

Tsukamoto T, Shimozawa N, Fujiki Y

机构信息

Meiji Institute of Health Science, Odawara, Kanagawa, Japan.

出版信息

Mol Cell Biol. 1994 Aug;14(8):5458-65. doi: 10.1128/mcb.14.8.5458-5465.1994.

Abstract

A cDNA encoding 35-kDa peroxisome assembly factor 1 (PAF-1), a peroxisomal integral membrane protein, was cloned from Chinese hamster ovary (CHO) cells and sequenced. The CHO PAF-1 comprised 304 amino acids, one residue shorter than rat or human PAF-1, and showed high homology to rat and human PAF-1: 90 and 86% at the nucleotide sequence level and 92 and 90% in amino acid sequence, respectively. PAF-1 from these three species contains a conserved cysteine-rich sequence at the C-terminal region which is exactly the same as that of a novel cysteine-rich RING finger motif family. PAF-1 cDNA from a peroxisome-deficient CHO cell mutant, Z65 (T. Tsukamoto, S. Yokota, and Y. Fujiki, J. Cell Biol. 110:651-660, 1990), contained a nonsense mutation at the codon for Trp-114, resulting in premature termination. Truncation in PAF-1 of either 19 amino acids from the N terminus or 92 residues from the C terminus maintained the peroxisome assembly-restoring activity when tested in both the Z65 mutant and the fibroblasts from a Zellweger patient. In contrast, deletion of 27 or 102 residues from the N or C terminus eliminated the activity. PAF-1 is encoded by free polysomal RNA, consistent with a general rule for biogenesis of peroxisomal proteins, including membrane polypeptides, implying the posttranslational transport and integration of PAF-1 into peroxisomal membrane.

摘要

从中国仓鼠卵巢(CHO)细胞中克隆并测序了一个编码35 kDa过氧化物酶体组装因子1(PAF-1)的cDNA,PAF-1是一种过氧化物酶体整合膜蛋白。CHO PAF-1由304个氨基酸组成,比大鼠或人类PAF-1少一个残基,并且与大鼠和人类PAF-1具有高度同源性:核苷酸序列水平分别为90%和86%,氨基酸序列水平分别为92%和90%。这三个物种的PAF-1在C末端区域含有一个保守的富含半胱氨酸的序列,该序列与一个新的富含半胱氨酸的RING指基序家族的序列完全相同。来自过氧化物酶体缺陷的CHO细胞突变体Z65(T. Tsukamoto、S. Yokota和Y. Fujiki,《细胞生物学杂志》110:651 - 660,1990)的PAF-1 cDNA在Trp-114密码子处含有一个无义突变,导致提前终止。当在Z65突变体和来自齐-韦二氏综合征患者的成纤维细胞中进行测试时,PAF-1从N末端截短19个氨基酸或从C末端截短92个残基仍保持过氧化物酶体组装恢复活性。相比之下,从N末端或C末端缺失27或102个残基则消除了该活性。PAF-1由游离多聚核糖体RNA编码,这与包括膜多肽在内的过氧化物酶体蛋白生物合成的一般规则一致,这意味着PAF-1在翻译后转运并整合到过氧化物酶体膜中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe8/359065/558004bb7518/molcellb00008-0452-a.jpg

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