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J. Biol. Chem., Vol. 265, Issue 8, 4711-4717, 03, 1990
JF Aitken, GP van Heusden, M Temkin and W Dowhan
Phosphatidylinositol transfer proteins (PI-TPs) catalyze the transfer of
phosphatidylinositol and phosphatidylcholine between membranes in vitro.
However, the in vivo function of these proteins is unknown. In this paper,
we use a combined biochemical and genetic approach to determine the
importance of PI-TP in vivo. An oligonucleotide based on the amino-terminal
sequence of the PI-TP from Saccharomyces cerevisiae was used to screen a
yeast genomic library for the gene encoding PI-TP (PIT1 gene). Positive
clones showed overproduction of transfer activities and transfer protein in
the 100,000 x g supernatants. The 5' terminus of the PIT1 gene correlates
with the predicted codons for residues 3-30 of the determined protein
sequence. A putative intron is located between the codons for residues 2
and 3 of the protein sequence. The codons for the first two amino acids of
the protein and the presumptive initiation methionine precede the intron.
Tetrad analysis of a heterozygous diploid (PIT1/pit1::LEU2) revealed that
the PIT1 gene is essential for cell growth. Nonviable spores could be
rescued by transformation of the above diploid prior to sporulation, with a
plasmid-borne copy of the wild type gene.
The gene encoding the phosphatidylinositol transfer protein is essential for cell growth
Department of Biochemistry and Molecular Biology, University of Texas Medical School, Houston 77225.
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