Snf1/AMP-activated protein kinase activates Arf3p to promote invasive yeast growth via a non-canonical GEF domain

Active GTP-bound Arf GTPases promote eukaryotic cell membrane trafficking and cytoskeletal remodelling. Arf activation is accelerated by guanine nucleotide-exchange factors (GEFs) using the critical catalytic glutamate in all known Sec7 domain sequences. Yeast Arf3p, a homologue of mammalian Arf6, i...

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Published inNature communications Vol. 6; no. 1; p. 7840
Main Authors Hsu, Jia-Wei, Chen, Kuan-Jung, Lee, Fang-Jen S.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 22.07.2015
Nature Publishing Group
Nature Pub. Group
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Summary:Active GTP-bound Arf GTPases promote eukaryotic cell membrane trafficking and cytoskeletal remodelling. Arf activation is accelerated by guanine nucleotide-exchange factors (GEFs) using the critical catalytic glutamate in all known Sec7 domain sequences. Yeast Arf3p, a homologue of mammalian Arf6, is required for yeast invasive responses to glucose depletion. Here we identify Snf1p as a GEF that activates Arf3p when energy is limited. SNF1 is the yeast homologue of AMP-activated protein kinase (AMPK), which is a key regulator of cellular energy homeostasis. As activation of Arf3p does not depend on the Snf1p kinase domain, assay of regulatory domain fragments yield evidence that the C-terminal hydrophobic α-helix core of Snf1p is a non-canonical GEF for Arf3p activation. Thus, our study reveals a novel mechanism for regulating cellular responses to energy deprivation, in particular invasive cell growth, through direct Arf activation by Snf1/AMPK. Snf1p is the yeast homologue of AMP-activated protein kinase, a key regulator of cellular energy homeostasis. Here, Hsu et al. identify Snf1p as a non-canonical guanine nucleotide-exchange factor for the Arf3p GTPase, regulating the yeast invasive response to glucose depletion.
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ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms8840