Role of ARHGEF3 as a GEF and mTORC2 Regulator

被引:1
|
作者
Khaliq, Sana Abdul [1 ,2 ]
Umair, Zobia [1 ]
Yoon, Mee-Sup [1 ,2 ,3 ]
机构
[1] Gachon Univ, Dept Mol Med, Coll Med, Incheon, South Korea
[2] Gachon Univ, Dept Hlth Sci & Technol, GAIHST, Incheon, South Korea
[3] Gachon Univ, Lee Gil Ya Canc & Diabet Inst, Incheon, South Korea
来源
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2022年 / 9卷
基金
新加坡国家研究基金会;
关键词
ARHGEF3; XPLN; rho guanine nucleotide exchange factors; mTORC2; Akt; NUCLEOTIDE-EXCHANGE FACTOR; RHO GTPASES; AUTOPHAGY; XPLN; ACTIVATION; EXPRESSION; PROTEIN; RHOGEFS; RISK; GENE;
D O I
10.3389/fcell.2021.806258
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Guanine nucleotide exchange factors (GEFs) activate GTPases by stimulating the release of guanosine diphosphate to permit the binding of guanosine triphosphate. ARHGEF3 or XPLN (exchange factor found in platelets, leukemic, and neuronal tissues) is a selective guanine nucleotide exchange factor for Rho GTPases (RhoGEFs) that activates RhoA and RhoB but not RhoC, RhoG, Rac1, or Cdc42. ARHGEF3 contains the diffuse B-cell lymphoma homology and pleckstrin homology domains but lacks similarity with other known functional domains. ARHGEF3 also binds the mammalian target of rapamycin complex 2 (mTORC2) and subsequently inhibits mTORC2 and Akt. In vivo investigation has also indicated the communication between ARHGEF3 and autophagy-related muscle pathologies. Moreover, studies on genetic variation in ARHGEF3 and genome-wide association studies have predicted exciting novel roles of ARHGEF3 in controlling bone mineral density, platelet formation and differentiation, and Hirschsprung disease. In conclusion, we hypothesized that additional biochemical and functional studies are required to elucidate the detailed mechanism of ARHGEF3-related pathologies and therapeutics.
引用
收藏
页数:7
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