A plasma-membrane E-MAP reveals links of the eisosome with sphingolipid metabolism and endosomal trafficking

被引:90
作者
Aguilar, Pablo S. [3 ]
Froehlich, Florian [2 ]
Rehman, Michael [2 ]
Shales, Mike [1 ]
Ulitsky, Igor [4 ]
Olivera-Couto, Agustina [3 ]
Braberg, Hannes [1 ]
Shamir, Ron [4 ]
Walter, Peter [5 ,6 ]
Mann, Matthias [7 ]
Ejsing, Christer S. [8 ]
Krogan, Nevan J. [1 ]
Walther, Tobias C. [2 ]
机构
[1] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
[2] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[3] Inst Pasteur Montevideo, Montevideo, Uruguay
[4] Tel Aviv Univ, Blavatnik Sch Comp Sci, IL-69978 Tel Aviv, Israel
[5] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[6] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[7] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[8] Univ So Denmark, Dept Biochem & Mol Biol, Odense, Denmark
基金
以色列科学基金会; 美国国家卫生研究院;
关键词
SACCHAROMYCES-CEREVISIAE; MASS-SPECTROMETRY; PROTEIN COMPLEXES; CONSERVED PROTEIN; PKH-KINASES; YEAST; GENES; LOCALIZATION; ENDOCYTOSIS; IDENTIFICATION;
D O I
10.1038/nsmb.1829
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The plasma membrane delimits the cell and controls material and information exchange between itself and the environment. How different plasma-membrane processes are coordinated and how the relative abundance of plasma-membrane lipids and proteins is homeostatically maintained are not yet understood. Here, we used a quantitative genetic interaction map, or E-MAP, to functionally interrogate a set of similar to 400 genes involved in various aspects of plasma-membrane biology, including endocytosis, signaling, lipid metabolism and eisosome function. From this E-MAP, we derived a set of 57,799 individual interactions between genes functioning in these various processes. Using triplet genetic motif analysis, we identified a new component of the eisosome, Eis1, and linked the poorly characterized gene EMP70 to endocytic and eisosome function. Finally, we implicated Rom2, a GDP/GTP exchange factor for Rho1 and Rho2, in the regulation of sphingolipid metabolism.
引用
收藏
页码:901 / U175
页数:9
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