Literature DB >> 19286980

Phosphatidylethanolamine is required for normal cell morphology and cytokinesis in the fission yeast Schizosaccharomyces pombe.

Jun Luo1, Yasuhiro Matsuo, Galina Gulis, Haylee Hinz, Jana Patton-Vogt, Stevan Marcus.   

Abstract

To investigate the contributions of phosphatidylethanolamine to the growth and morphogenesis of the fission yeast Schizosaccharomyces pombe, we have characterized three predicted genes in this organism, designated psd1, psd2, and psd3, encoding phosphatidylserine decarboxylases, which catalyze the conversion of phosphatidylserine to phosphatidylethanolamine in both eukaryotic and prokaryotic organisms. S. pombe mutants carrying deletions in any one or two psd genes are viable in complex rich medium and synthetic defined minimal medium. However, mutants carrying deletions in all three psd genes (psd1-3Delta mutants) grow slowly in rich medium and are inviable in minimal medium, indicating that the psd1 to psd3 gene products share overlapping essential cellular functions. Supplementation of growth media with ethanolamine, which can be converted to phosphatidylethanolamine by the Kennedy pathway, restores growth to psd1-3Delta cells in minimal medium, indicating that phosphatidylethanolamine is essential for S. pombe cell growth. psd1-3Delta cells produce lower levels of phosphatidylethanolamine than wild-type cells, even in medium supplemented with ethanolamine, indicating that the Kennedy pathway can only partially compensate for the loss of phosphatidylserine decarboxylase activity in S. pombe. psd1-3Delta cells appear morphologically indistinguishable from wild-type S. pombe cells in medium supplemented with ethanolamine, but when cultured in nonsupplemented medium, they produce high frequencies of abnormally shaped cells as well as cells exhibiting severe septation defects, including multiple, mispositioned, deformed, and misoriented septa. Our results demonstrate that phosphatidylethanolamine is essential for cell growth and for normal cytokinesis and cellular morphogenesis in S. pombe, and they illustrate the usefulness of this model eukaryote for investigating potentially conserved biological and molecular functions of phosphatidylethanolamine.

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Year:  2009        PMID: 19286980      PMCID: PMC2681608          DOI: 10.1128/EC.00029-09

Source DB:  PubMed          Journal:  Eukaryot Cell        ISSN: 1535-9786


  38 in total

Review 1.  C2-domains, structure and function of a universal Ca2+-binding domain.

Authors:  J Rizo; T C Südhof
Journal:  J Biol Chem       Date:  1998-06-26       Impact factor: 5.157

Review 2.  Phosphatidylserine decarboxylase.

Authors:  D R Voelker
Journal:  Biochim Biophys Acta       Date:  1997-09-04

3.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.

Authors:  J D Thompson; D G Higgins; T J Gibson
Journal:  Nucleic Acids Res       Date:  1994-11-11       Impact factor: 16.971

4.  Phosphatidylserine synthetase mutants of Escherichia coli. Genetic mapping and membrane phospholipid composition.

Authors:  C R Raetz
Journal:  J Biol Chem       Date:  1976-06-10       Impact factor: 5.157

5.  Metabolism of labeled lysolecithin, lysophosphatidyl ethanolamine and lecithin in the rat.

Authors:  Y Stein; O Stein
Journal:  Biochim Biophys Acta       Date:  1966-02-01

6.  Sequence and inactivation of the pss gene of Escherichia coli. Phosphatidylethanolamine may not be essential for cell viability.

Authors:  A DeChavigny; P N Heacock; W Dowhan
Journal:  J Biol Chem       Date:  1991-03-15       Impact factor: 5.157

7.  Redistribution of phosphatidylethanolamine at the cleavage furrow of dividing cells during cytokinesis.

Authors:  K Emoto; T Kobayashi; A Yamaji; H Aizawa; I Yahara; K Inoue; M Umeda
Journal:  Proc Natl Acad Sci U S A       Date:  1996-11-12       Impact factor: 11.205

8.  Phosphatidylserine decarboxylase from Saccharomyces cerevisiae. Isolation of mutants, cloning of the gene, and creation of a null allele.

Authors:  P J Trotter; J Pedretti; D R Voelker
Journal:  J Biol Chem       Date:  1993-10-05       Impact factor: 5.157

9.  Identification of a non-mitochondrial phosphatidylserine decarboxylase activity (PSD2) in the yeast Saccharomyces cerevisiae.

Authors:  P J Trotter; D R Voelker
Journal:  J Biol Chem       Date:  1995-03-17       Impact factor: 5.157

10.  Isolation of the yeast structural gene for the membrane-associated enzyme phosphatidylserine synthase.

Authors:  V A Letts; L S Klig; M Bae-Lee; G M Carman; S A Henry
Journal:  Proc Natl Acad Sci U S A       Date:  1983-12       Impact factor: 11.205

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7.  ER-localized phosphatidylethanolamine synthase plays a conserved role in lipid droplet formation.

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8.  Cytokinesis-based constraints on polarized cell growth in fission yeast.

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  8 in total

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