Smith Jennifer J, Marelli Marcello, Christmas Rowan H, Vizeacoumar Franco J, Dilworth David J, Ideker Trey, Galitski Timothy, Dimitrov Krassen, Rachubinski Richard A, Aitchison John D
The Institute for Systems Biology, 1441 N. 34th Street, Seattle, WA 98103-8904, USA.
J Cell Biol. 2002 Jul 22;158(2):259-71. doi: 10.1083/jcb.200204059.
Yeast cells were induced to proliferate peroxisomes, and microarray transcriptional profiling was used to identify PEX genes encoding peroxins involved in peroxisome assembly and genes involved in peroxisome function. Clustering algorithms identified 224 genes with expression profiles similar to those of genes encoding peroxisomal proteins and genes involved in peroxisome biogenesis. Several previously uncharacterized genes were identified, two of which, YPL112c and YOR084w, encode proteins of the peroxisomal membrane and matrix, respectively. Ypl112p, renamed Pex25p, is a novel peroxin required for the regulation of peroxisome size and maintenance. These studies demonstrate the utility of comparative gene profiling as an alternative to functional assays to identify genes with roles in peroxisome biogenesis.
诱导酵母细胞增殖过氧化物酶体,并利用微阵列转录谱分析来鉴定编码参与过氧化物酶体组装的过氧化物酶的PEX基因以及参与过氧化物酶体功能的基因。聚类算法鉴定出224个基因,其表达谱与编码过氧化物酶体蛋白的基因以及参与过氧化物酶体生物发生的基因相似。鉴定出了几个以前未表征的基因,其中两个,YPL112c和YOR084w,分别编码过氧化物酶体膜和基质的蛋白质。重新命名为Pex25p的Ypl112p是调节过氧化物酶体大小和维持所必需的一种新型过氧化物酶。这些研究证明了比较基因谱分析作为一种替代功能测定来鉴定参与过氧化物酶体生物发生的基因的实用性。