Protein Trafficking or Cell Signaling: A Dilemma for the Adaptor Protein TOM1

被引:13
|
作者
Roach, Tiffany G. [1 ,2 ]
Lang, Helja K. M. [3 ,4 ,5 ,6 ,7 ]
Xiong, Wen [1 ,2 ,8 ]
Ryhanen, Samppa J. [3 ,4 ,5 ]
Capelluto, Daniel G. S. [1 ,2 ]
机构
[1] Virginia Tech, Prot Signaling Domains Lab, Dept Biol Sci, Fralin Life Sci Inst, Blacksburg, VA 24061 USA
[2] Virginia Tech, Ctr Soft Matter & Biol Phys, Blacksburg, VA 24061 USA
[3] Univ Helsinki, Div Hematol Oncol & Stem Cell Transplantat, Childrens Hosp, Helsinki, Finland
[4] Univ Helsinki, Pediat Res Ctr, New Childrens Hosp, Helsinki, Finland
[5] Helsinki Univ Hosp, Helsinki, Finland
[6] Univ Helsinki, Dept Anat & Stem Cells, Fac Med, Helsinki, Finland
[7] Univ Helsinki, Metab Res Program, Fac Med, Helsinki, Finland
[8] Baylor Coll Med, Huffington Ctr Aging, Houston, TX 77030 USA
关键词
TOM1; TOL; endosome; ESCRT; TOLLIP; Endofin; phosphoinositides; C-13 RESONANCE ASSIGNMENTS; STRUCTURAL BASIS; VHS DOMAIN; UBIQUITIN RECOGNITION; NEGATIVE REGULATOR; BACKBONE H-1; MYOSIN VI; TOLLIP; ENDOCYTOSIS; ENDOSOMES;
D O I
10.3389/fcell.2021.643769
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Lysosomal degradation of ubiquitinated transmembrane protein receptors (cargo) relies on the function of Endosomal Sorting Complex Required for Transport (ESCRT) protein complexes. The ESCRT machinery is comprised of five unique oligomeric complexes with distinct functions. Target of Myb1 (TOM1) is an ESCRT protein involved in the initial steps of endosomal cargo sorting. To exert its function, TOM1 associates with ubiquitin moieties on the cargo via its VHS and GAT domains. Several ESCRT proteins, including TOLLIP, Endofin, and Hrs, have been reported to form a complex with TOM1 at early endosomal membrane surfaces, which may potentiate the role of TOM1 in cargo sorting. More recently, it was found that TOM1 is involved in other physiological processes, including autophagy, immune responses, and neuroinflammation, which crosstalk with its endosomal cargo sorting function. Alteration of TOM1 function has emerged as a phosphoinositide-dependent survival mechanism for bacterial infections and cancer progression. Based on current knowledge of TOM1-dependent cellular processes, this review illustrates how TOM1 functions in coordination with an array of protein partners under physiological and pathological scenarios.
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页数:11
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