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A Conserved Phosphatase Cascade that Regulates Nuclear Membrane Biogenesis
Author(s) -
Kim Youngjun
Publication year - 2008
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.22.1_supplement.1048.1
Subject(s) - biogenesis , phosphatase , yeast , biology , microbiology and biotechnology , saccharomyces cerevisiae , biochemistry , conserved sequence , nuclear localization sequence , regulator , protein phosphatase 2 , inner membrane , peptide sequence , phosphorylation , gene , mitochondrion
A newly emerging family of phosphatases that are members of the haloacid dehalogenase superfamily contain the catalytic motif DXDX(T/V). A member of this DXDX(T/V) phosphatase family known as Dullard was recently shown to be a potential regulator of neural tube development in Xenopus. (Satow R., et al (2002) Biochem. Biophys. Res. Commun. 295, 85–91). Herein, we demonstrate that human Dullard and the yeast protein Nem1p perform similar functions in mammalian cells and yeast cells, respectively. In addition to similarity in primary sequence, Dullard and Nem1p possess similar domains, they show similar substrate preferences, and both localize to the nuclear envelope. Additionally, we show that human Dullard can rescue the aberrant nuclear envelope morphology of nem1∆ yeast cells, functionally replacing Nem1p. Finally, Nem1p, has been shown to deposphorylate the yeast phosphatidic acid phosphatase Smp2p (Santos‐Rosa et al (2005) EMBO J 24, 1931–41) and we show that Dullard dephosphorylates the mammalian phospatidic acid phosphatase, lipin. Therefore, we propose that Dullard participates in a unique phosphatase cascade regulating nuclear membrane biogenesis and that this cascade is conserved from yeast to mammals