Exaptive Evolution of Target of Rapamycin Signaling in Multicellular Eukaryotes

被引:50
|
作者
Brunkard, Jacob O. [1 ,2 ,3 ]
机构
[1] Univ Calif Berkeley, Dept Plant & Microbial Biol, Berkeley, CA 94720 USA
[2] ARS, Plant Gene Express Ctr, USDA, Albany, CA 94710 USA
[3] Univ Wisconsin, Lab Genet, Madison, WI 53706 USA
关键词
TRANSFER-RNA SYNTHETASE; AMINO-ACID SUFFICIENCY; ARABIDOPSIS-THALIANA; INTERCELLULAR TRANSPORT; RIBOSOME BIOGENESIS; GENE-EXPRESSION; LEUCINE SENSOR; TOR DEFICIENCY; PLANT-GROWTH; PATHWAY;
D O I
10.1016/j.devcel.2020.06.022
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Target of rapamycin (TOR) is a protein kinase that coordinates metabolism with nutrient and energy availability in eukaryotes. TOR and its primary interactors, RAPTOR and LST8, have been remarkably evolutionarily static since they arose in the unicellular last common ancestor of plants, fungi, and animals, but the upstream regulatory mechanisms and downstream effectors of TOR signaling have evolved considerable diversity in these separate lineages. Here, I focus on the roles of exaptation and adaptation in the evolution of novel signaling axes in the TOR network in multicellular eukaryotes, concentrating especially on amino acid sensing, cell-cell signaling, and cell differentiation.
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页码:142 / 155
页数:14
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