A conserved signaling network monitors delivery of sphingolipids to the plasma membrane in budding yeast

Author:

Clarke Jesse1,Dephoure Noah2,Horecka Ira1,Gygi Steven3,Kellogg Douglas1

Affiliation:

1. Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, Santa Cruz, CA 95064

2. Department of Biochemistry, Weill Cornell Medical College, New York, NY 10021

3. Department of Cell Biology, Harvard Medical School, Boston, MA 02115

Abstract

In budding yeast, cell cycle progression and ribosome biogenesis are dependent on plasma membrane growth, which ensures that events of cell growth are coordinated with each other and with the cell cycle. However, the signals that link the cell cycle and ribosome biogenesis to membrane growth are poorly understood. Here we used proteome-wide mass spectrometry to systematically discover signals associated with membrane growth. The results suggest that membrane trafficking events required for membrane growth generate sphingolipid-dependent signals. A conserved signaling network appears to play an essential role in signaling by responding to delivery of sphingolipids to the plasma membrane. In addition, sphingolipid-dependent signals control phosphorylation of protein kinase C (Pkc1), which plays an essential role in the pathways that link the cell cycle and ribosome biogenesis to membrane growth. Together these discoveries provide new clues as to how growth-­dependent signals control cell growth and the cell cycle.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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