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MBC in Press, published online ahead of print May 28, 2004
Mol. Biol. Cell 10.1091/mbc.E03-09-0680

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Submitted on September 18, 2003
Revised on May 10, 2004
Accepted on May 16, 2004

Characterisation of the Saccharomyces cerevisiae Fol1 Protein: Starvation for C1 Carrier Induces Pseudohyphal Growth

Ulrich Gueldener*{dagger}{ddagger}, Gabriele J. Koehler*{ddagger}, Christoph Haussmann{sect}, Adelbert Bacher{sect}, Jörn Kricke||, Dietmar Becher¶, and Johannes H. Hegemann*#

*Funktionelle Genomforschung der Mikroorganismen, Heinrich-Heine-Universität, 40225 Düsseldorf, Germany; {sect}Institut für Organische Chemie und Biochemie, Technische Universität München, 85747 Garching, Germany; ||AG Anatomie und Zellbiologie der Charite, 13353 Berlin, Germany; and MICROMUN Private Institute for Microbiological Research GmbH, Biotechnikum Greifswald, 17489 Greifswald, Germany

Monitoring Editor: Douglas Koshland

Tetrahydrofolate (vitamin B9) and its folate derivatives are essential cofactors in one-carbon (C1) transfer reactions and absolutely required for the synthesis of a variety of different compounds including methionine and purines. Most plants, microbial eukaryotes and prokaryotes synthesize folate de novo. We have characterized an important enzyme in this pathway, the S. cerevisiae FOL1 gene. Expression of the budding yeast gene FOL1 in E. coli identified the folate biosynthetic enzyme activities dihydroneopterin aldolase (DHNA), 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase (HPPK),and dihydropteroate synthase (DHPS). All 3 enzyme activities were also detected in wild-type yeast strains, while fol1{Delta} deletion strains only showed background activities thus demonstrating that Fol1p catalyzes three sequential steps of the tetrahydrofolate biosynthetic pathway and thus is the central enzyme of this pathway which starting from GTP consists of 7 enzymatic reactions in total. Fol1p is exclusively localized to mitochondria as shown by fluorescence microscopy and immune electron microscopy. FOL1 is an essential gene and the nongrowth phenotype of the fol1 deletion leads to a recessive auxotrophy for folinic acid (5'-formyltetrahydrofolate). Growth of the fol1{Delta} deletion strain on folinic acid supplemented rich media induced a dimorphic switch with haploid invasive and filamentous pseudohyphal growth in the presence of glucose and ammonium which are known suppressors of filamentous and invasive growth. The invasive growth phenotype induced by the depletion of C1 carrier is dependent on the transcription factor Ste12p and the flocullin/adhesin Flo11p, while the filamentation phenotype is independent of Ste12p, Tec1p, Phd1p and Flo11p suggesting other signaling pathways as well as other adhesion proteins.


{dagger}Present address: Institute of Bioinformatics, GSF - National Research Center for Environment and Health, Ingolstädter Landstraße 1, 85764 Neuherberg, Germany

{ddagger}These authors contributed equally to this work

#Corresponding author.

Johannes H. Hegemann, E-mail: hegemann{at}uni-duesseldorf.de




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