Structure and Expression of Mammalian Peroxisome Assembly Factor-1 (PMP35) Genes

Wilson G.N., Bryant D.D.
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引用次数: 4

Abstract

Mammalian genes encoding a 35-kDa peroxisomal membrane protein (PMP35, peroxisome assembly factor-1) are compared using the polymerase chain reaction and DNA sequencing. DNA sequencing of the 915 bp of the PMP35 coding regions was in complete agreement with previously published rat data and showed 36 and 133 nucleotide substitutions, respectively, in mouse and man. The 12 and 35 respective amino acid changes encoded by these nucleotide substitutions are clustered and compatible with putative membrane-spanning regions. Rat/human and rat/mouse comparisons yield silent mutation rates of 0.33 and 0.21% per site per million years and replacement mutation rates of 0.082 and 0.076%; transitions account for 67% (human/mouse) and 83% (rat/mouse) of nucleotide replacements among PMP35 genes. PMP35 gene expression in mouse tissues as measured by reverse transcriptase-PCR was responsive to clofibrate and disproportionately high in neural tissue.

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哺乳动物过氧化物酶体组装因子-1 (PMP35)基因的结构与表达
利用聚合酶链反应和DNA测序技术,比较了编码35 kda过氧化物酶体膜蛋白(PMP35,过氧化物酶体组装因子-1)的哺乳动物基因。PMP35编码区915 bp的DNA测序与先前发表的大鼠数据完全一致,在小鼠和人类中分别显示36和133个核苷酸替换。由这些核苷酸取代编码的12和35个氨基酸变化是聚集的,并且与假定的跨膜区域兼容。大鼠/人类和大鼠/小鼠的比较结果显示,每百万年每个位点的沉默突变率分别为0.33和0.21%,替代突变率分别为0.082和0.076%;在PMP35基因中,转换占核苷酸替换的67%(人/小鼠)和83%(大鼠/小鼠)。通过逆转录- pcr检测小鼠组织中的PMP35基因表达对氯贝特有反应,在神经组织中的表达过高。
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