Pip2p: A transcriptional regulator of peroxisome proliferation in the yeast Saccharomyces cerevisiae

被引:82
作者
Rottensteiner, H
Kal, AJ
Filipits, M
Binder, M
Hamilton, B
Tabak, HF
Ruis, H
机构
[1] UNIV VIENNA, VIENNA BIOCTR, INST BIOCHEM & MOLEK ZELLBIOL, A-1030 VIENNA, AUSTRIA
[2] LUDWIG BOLTZMANN FORSCHUNGSSTELLE BIOCHEM, A-1030 VIENNA, AUSTRIA
[3] UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, 1105 AZ AMSTERDAM, NETHERLANDS
[4] UNIV VIENNA, INST TUMORBIOL KREBSFORSCH, A-1090 VIENNA, AUSTRIA
关键词
ORE; peroxisome proliferation; PIP2; saccharomyces cerevisiae; yeast;
D O I
10.1002/j.1460-2075.1996.tb00655.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In Saccharomyces cerevisiae, peroxisomes are the exclusive site for the degradation of fatty acids, Upon growth with the fatty acid oleic acid as sole carbon source, not only are the enzymes of beta-oxidation and catalase A induced, but also the peroxisomal compartment as a whole increases in volume and the number of organelles per cell rises, We previously identified a cis-acting DNA sequence [oleate response element (ORE)] involved in induction of genes encoding peroxisomal proteins, The aim of our investigation was to test whether a single mechanism acting via the ORE coordinates the events necessary for the proliferation of an entire organelle, Here we report the cloning and characterization of the oleate-specific transcriptional activator protein Pip2p (pip: peroxisome induction pathway), Pip2p contains a typical Zn(2)-Cys(6) cluster domain and binds to OREs, A pip2 deletion strain is impaired in growth on oleate as sole carbon source and the induction of beta-oxidation enzymes is abolished, Moreover, only a few, small peroxisomes per cell can be detected. These results indicate that fatty acids activate Pip2p, which in turn activates the transcription of genes encoding beta-oxidation components and acts as the crucial activator of peroxisomes.
引用
收藏
页码:2924 / 2934
页数:11
相关论文
共 57 条
[21]  
HILTUNEN JK, 1992, J BIOL CHEM, V267, P6646
[22]  
ISSEMANN I, 1990, NATURE, V347, P645, DOI 10.1038/347645a0
[23]   THE PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR RETINOID-X RECEPTOR HETERODIMER IS ACTIVATED BY FATTY-ACIDS AND FIBRATE HYPOLIPEMIC DRUGS [J].
ISSEMANN, I ;
PRINCE, RA ;
TUGWOOD, JD ;
GREEN, S .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 1993, 11 (01) :37-47
[24]   TRANSFORMATION OF INTACT YEAST-CELLS TREATED WITH ALKALI CATIONS [J].
ITO, H ;
FUKUDA, Y ;
MURATA, K ;
KIMURA, A .
JOURNAL OF BACTERIOLOGY, 1983, 153 (01) :163-168
[25]   A MODEL FUNGAL GENE REGULATORY MECHANISM - THE GAL GENES OF SACCHAROMYCES-CEREVISIAE [J].
JOHNSTON, M .
MICROBIOLOGICAL REVIEWS, 1987, 51 (04) :458-476
[26]   INTERACTION OF POSITIVE AND NEGATIVE REGULATORY PROTEINS IN THE GALACTOSE REGULON OF YEAST [J].
JOHNSTON, SA ;
SALMERON, JM ;
DINCHER, SS .
CELL, 1987, 50 (01) :143-146
[27]  
JONES EW, 1977, GENETICS, V85, P23
[28]   FATTY-ACIDS AND RETINOIDS CONTROL LIPID-METABOLISM THROUGH ACTIVATION OF PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR RETINOID-X RECEPTOR HETERODIMERS [J].
KELLER, H ;
DREYER, C ;
MEDIN, J ;
MAHFOUDI, A ;
OZATO, K ;
WAHLI, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (06) :2160-2164
[29]   EXPRESSION OF GENES ENCODING PEROXISOMAL PROTEINS IN SACCHAROMYCES-CEREVISIAE IS REGULATED BY DIFFERENT CIRCUITS OF TRANSCRIPTIONAL CONTROL [J].
KOS, W ;
KAL, AJ ;
VANWILPE, S ;
TABAK, HF .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1995, 1264 (01) :79-86
[30]   2 INDEPENDENT PEROXISOMAL TARGETING SIGNALS IN CATALASE-A OF SACCHAROMYCES-CEREVISIAE [J].
KRAGLER, F ;
LANGEDER, A ;
RAUPACHOVA, J ;
BINDER, M ;
HARTIG, A .
JOURNAL OF CELL BIOLOGY, 1993, 120 (03) :665-673