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The Hansenula polymorpha PER9 Gene Encodes a Peroxisomal Membrane Protein Essential for Peroxisome Assembly and Integrity

Baerends, R. J. S., Rasmussen, S. W., Hilbrands, R. E., Heide, M. V. D., Faber, K. N., Reuvekamp, P. T. W., Kiel, J. A. K. W., Cregg, J. M., Klei, I. J. V. D., Veenhuis, M., vanderHeide, M. & VanderKlei, I. J., 12-Apr-1996, In : The Journal of Biological Chemistry. 271, 15, p. 8887 - 8894 8 p.

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We have cloned and characterized the Hansenula polymorpha PER9 gene by functional complementation of the per9-1 mutant of H. polymorpha, which is defective in peroxisome biogenesis. The predicted product, Per9p, is a polypeptide of 52 kDa with sequence similarity to Pas3p, a protein involved in peroxisome biogenesis in Saccharomyces cerevisiae. In a per9 disruption strain (Δper9), peroxisomal matrix and membrane proteins are present at wild-type levels. The matrix proteins accumulated in the cytoplasm. However, the location of the membrane proteins remained obscure; fully induced Δper9 cells lacked residual peroxisomal vesicles (“ghosts”). Analysis of the activity of the PER9 promoter revealed that PER9 expression was low in cells grown on glucose, but was enhanced during growth of cells on peroxisome-inducing substrates. The highest expression levels were observed in cells grown on methanol. Localization studies revealed that Per9p is an integral membrane protein of the peroxisome. Targeting studies suggested that Per9p may be sorted to the peroxisome via the endoplasmic reticulum. Overexpression of PER9 induced a significant increase in the number of peroxisomes per cell, a result that suggests that Per9p may be involved in peroxisome proliferation and/or membrane biosynthesis. When PER9 expression was placed under the control of a strongly regulatable promoter and switched off, peroxisomes were observed to disintegrate over time in a manner that suggested that Per9p may be required for maintenance of the peroxisomal membrane.
Original languageEnglish
Pages (from-to)8887 - 8894
Number of pages8
JournalThe Journal of Biological Chemistry
Volume271
Issue number15
Publication statusPublished - 12-Apr-1996

    Keywords

  • RAT-LIVER PEROXISOMES, ZELLWEGER SYNDROME, TARGETING SIGNAL, ALCOHOL OXIDASE, BIOGENESIS, CLONING, IMPORT, ORGANELLE, CATALASE, MUTANTS

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