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Functional Classification of Arabidopsis Peroxisome Biogenesis Factors Proposed from Analyses of Knockdown Mutants

机译:从击倒突变体的分析建议拟南芥过氧化物酶体生物发生因子的功能分类。

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In higher plants, peroxisomes accomplish a variety of physiological functions such as lipid catabolism, photorespiration and hormone biosynthesis. Recently, many factors regulating peroxisomal biogenesis, so-called PEX genes, have been identified not only in plants but also in yeasts and mammals. In the Arabidopsis genome, the presence of at least 22 PEX genes has been proposed. Here, we clarify the physiological functions of 18 PEX genes for peroxisomal biogenesis by analyzing transgenic Arabidopsis plants that suppressed the PEX gene expression using RNA interference. The results indicated that the function of these PEX genes could be divided into two groups. One group involves PEX1, PEX2, PEX4, PEX6, PEX10, PEX12 and PEX13 together with previously characterized PEX5, PEX7 and PEX14. Defects in these genes caused loss of peroxisomal function due to misdistribution of peroxisomal matrix proteins in the cytosol. Of these, the pex10 mutant showed pleiotropic phenotypes that were not observed in any other pex mutants. In contrast, reduced peroxisomal function of the second group, including PEX3, PEX11, PEX16 and PEX19, was induced by morphological changes of the peroxisomes. Cells of the pex16 mutant in particular possessed reduced numbers of large peroxisome(s) that contained unknown vesicles. These results provide experimental evidence indicating that all of these PEX genes play pivotal roles in regulating peroxisomal biogenesis. We conclude that PEX genes belonging to the former group are involved in regulating peroxisomal protein import, whereas those of the latter group are important in maintaining the structure of peroxisome.
机译:在高等植物中,过氧化物酶体完成了多种生理功能,例如脂质分解代谢,光呼吸和激素生物合成。最近,不仅在植物中而且在酵母和哺乳动物中已经发现了许多调节过氧化物酶体生物发生的因素,即所谓的PEX基因。在拟南芥基因组中,已经提出了至少22个PEX基因的存在。在这里,我们通过分析使用RNA干扰抑制PEX基因表达的转基因拟南芥植物,阐明了18个PEX基因对于过氧化物酶体生物发生的生理功能。结果表明,这些PEX基因的功能可分为两组。一组涉及PEX1,PEX2,PEX4,PEX6,PEX10,PEX12和PEX13,以及先前表征的PEX5,PEX7和PEX14。由于过氧化物酶体基质蛋白在细胞质中的分布不正确,这些基因的缺陷导致了过氧化物酶体功能的丧失。其中,pex10突变体表现出多效性表型,在任何其他pex突变体中均未观察到。相反,第二组的过氧化物酶体功能降低,是由过氧化物酶体的形态变化引起的,包括PEX3,PEX11,PEX16和PEX19。尤其是pex16突变体的细胞具有减少数量的含有未知囊泡的大过氧化物酶体。这些结果提供了实验证据,表明所有这些PEX基因在调节过氧化物酶体生物发生中起关键作用。我们得出的结论是,属于前一组的PEX基因参与调节过氧化物酶体蛋白的导入,而后一组的PEX基因在维持过氧化物酶体的结构中很重要。

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