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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.

DOI:10.1128/mcb.14.8.5458-5465.1994
PMID:8035823
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC359065/
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/b8454926098c/molcellb00008-0456-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe8/359065/558004bb7518/molcellb00008-0452-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe8/359065/616ed70adbcc/molcellb00008-0452-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe8/359065/a6f6d5e4f540/molcellb00008-0453-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe8/359065/0f301812c9ae/molcellb00008-0455-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe8/359065/b8454926098c/molcellb00008-0456-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe8/359065/558004bb7518/molcellb00008-0452-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe8/359065/616ed70adbcc/molcellb00008-0452-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe8/359065/a6f6d5e4f540/molcellb00008-0453-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe8/359065/0f301812c9ae/molcellb00008-0455-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe8/359065/b8454926098c/molcellb00008-0456-a.jpg

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Peroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis.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。
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本文引用的文献

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Peroxisome-deficient Chinese hamster ovary cells with point mutations in peroxisome assembly factor-1.在过氧化物酶体组装因子-1中存在点突变的过氧化物酶体缺陷型中国仓鼠卵巢细胞。
J Biol Chem. 1993 Jun 15;268(17):12631-6.
2
Identification and preliminary characterization of a protein motif related to the zinc finger.一种与锌指相关的蛋白质基序的鉴定及初步表征
Proc Natl Acad Sci U S A. 1993 Mar 15;90(6):2112-6. doi: 10.1073/pnas.90.6.2112.
3
Absence of DNA in peroxisomes of Candida tropicalis.热带假丝酵母过氧化物酶体中无DNA。
Plant Mol Biol. 1998 Sep;38(1-2):163-89.
4
PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p.PEX12,III型泽尔韦格综合征的致病基因:通过对CHO细胞突变体进行功能互补克隆cDNA、患者分析及PEX12p的特性研究
Mol Cell Biol. 1998 Jul;18(7):4324-36. doi: 10.1128/MCB.18.7.4324.
5
Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.通过在CHO细胞突变体上进行功能互补克隆得到的人类PEX1,与互补组I的过氧化物酶体缺陷型泽尔韦格综合征有关。
Proc Natl Acad Sci U S A. 1998 Apr 14;95(8):4350-5. doi: 10.1073/pnas.95.8.4350.
6
Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants.过氧化物酶体靶向信号1型(PTS1)受体参与PTS1和PTS2的导入:对PEX5缺陷型CHO细胞突变体的研究
Mol Cell Biol. 1998 Jan;18(1):388-99. doi: 10.1128/MCB.18.1.388.
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Functional identification of a Leishmania gene related to the peroxin 2 gene reveals common ancestry of glycosomes and peroxisomes.一个与过氧化物酶2基因相关的利什曼原虫基因的功能鉴定揭示了糖体和过氧化物酶体的共同起源。
Mol Cell Biol. 1997 Mar;17(3):1093-101. doi: 10.1128/MCB.17.3.1093.
8
The Pichia pastoris PER6 gene product is a peroxisomal integral membrane protein essential for peroxisome biogenesis and has sequence similarity to the Zellweger syndrome protein PAF-1.巴斯德毕赤酵母PER6基因产物是一种过氧化物酶体生物发生所必需的过氧化物酶体整合膜蛋白,与泽尔韦格综合征蛋白PAF-1具有序列相似性。
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Mol Cell Biol. 1995 Nov;15(11):6406-19. doi: 10.1128/MCB.15.11.6406.
J Bacteriol. 1982 Oct;152(1):269-74. doi: 10.1128/jb.152.1.269-274.1982.
4
Synthesis of a major integral membrane polypeptide of rat liver peroxisomes on free polysomes.大鼠肝脏过氧化物酶体主要整合膜多肽在游离多聚核糖体上的合成。
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5
Acyl-Coa oxidase and hydratase-dehydrogenase, two enzymes of the peroxisomal beta-oxidation system, are synthesized on free polysomes of clofibrate-treated rat liver.酰基辅酶A氧化酶和水化酶-脱氢酶是过氧化物酶体β-氧化系统的两种酶,在氯贝丁酯处理的大鼠肝脏游离多核糖体上合成。
J Cell Biol. 1984 Dec;99(6):2241-6. doi: 10.1083/jcb.99.6.2241.
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Synthesis of 3-ketoacyl-CoA thiolase of rat liver peroxisomes on free polyribosomes as a larger precursor. Induction of thiolase mRNA activity by clofibrate.大鼠肝脏过氧化物酶体3-酮酰基辅酶A硫解酶在游离多核糖体上作为更大的前体合成。氯贝丁酯对硫解酶mRNA活性的诱导作用。
Biochem J. 1985 Mar 15;226(3):697-704. doi: 10.1042/bj2260697.
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Biogenesis of peroxisomes.过氧化物酶体的生物发生
Annu Rev Cell Biol. 1985;1:489-530. doi: 10.1146/annurev.cb.01.110185.002421.
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Rapid and efficient site-specific mutagenesis without phenotypic selection.无需表型筛选的快速高效位点特异性诱变。
Proc Natl Acad Sci U S A. 1985 Jan;82(2):488-92. doi: 10.1073/pnas.82.2.488.
9
How proteins get into microbodies (peroxisomes, glyoxysomes, glycosomes).蛋白质如何进入微体(过氧化物酶体、乙醛酸循环体、糖体)。
Biochim Biophys Acta. 1986 May 5;866(4):179-203. doi: 10.1016/0167-4781(86)90044-8.
10
Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly.缺乏缩醛磷脂生物合成和过氧化物酶体组装的动物细胞突变体的分离。
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