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Updated: Dec 13, 2025

An In Vitro Assay to Detect tRNA-Isopentenyl Transferase Activity
Published on: October 8, 2018
Roles of aminoacyl-tRNA synthetase-interacting multi-functional proteins in physiology and cancer
Zheng Zhou1, Bao Sun2,3, Shiqiong Huang4
1Department of Chinese Medicine, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450000, China.
Abstract:
Aminoacyl-tRNA synthetases (ARSs) are an important class of enzymes with an evolutionarily conserved mechanism for protein synthesis. In higher eukaryotic systems, eight ARSs and three ARS-interacting multi-functional proteins (AIMPs) form a multi-tRNA synthetase complex (MSC), which seems to contribute to cellular homeostasis. Of these, AIMPs are generally considered as non-enzyme factors, playing a scaffolding role during MSC assembly. Although the functions of AIMPs are not fully understood, increasing evidence indicates that these scaffold proteins usually exert tumor-suppressive activities. In addition, endothelial monocyte-activating polypeptide II (EMAP II), as a cleavage product of AIMP1, and AIMP2-DX2, as a splice variant of AIMP2 lacking exon 2, also have a pivotal role in regulating tumorigenesis. In this review, we summarize the biological functions of AIMP1, EMAP II, AIMP2, AIMP2-DX2, and AIMP3. Also, we systematically introduce their emerging roles in cancer, aiming to provide new ideas for the treatment of cancer.
Insights
Aminoacyl-tRNA synthetases (ARSs) and their interacting proteins (AIMPs) are crucial for cellular homeostasis. This review explores their roles in cancer, highlighting potential therapeutic strategies.
Area of Science:
- Biochemistry
- Molecular Biology
- Oncology
Background:
- Aminoacyl-tRNA synthetases (ARSs) are essential enzymes for protein synthesis.
- ARS-interacting multi-functional proteins (AIMPs) form a complex (MSC) involved in cellular homeostasis.
- AIMPs, though non-enzymatic, are increasingly recognized for tumor-suppressive functions.
Purpose of the Study:
- To review the biological functions of AIMP1, EMAP II, AIMP2, AIMP2-DX2, and AIMP3.
- To systematically introduce the emerging roles of these proteins in cancer.
- To offer novel insights for cancer treatment strategies.
Main Methods:
- Literature review of existing research on ARSs and AIMPs.
- Analysis of functional roles and cancer-related activities.
- Synthesis of information on AIMP1, EMAP II, AIMP2, AIMP2-DX2, and AIMP3.
Main Results:
- AIMPs play a scaffolding role in the MSC and exhibit tumor-suppressive activities.
- EMAP II (AIMP1 cleavage product) and AIMP2-DX2 (AIMP2 splice variant) are implicated in tumorigenesis.
- The reviewed proteins demonstrate diverse biological functions with significant implications in cancer.
Conclusions:
- AIMP family proteins and their derivatives have critical roles in cancer development and progression.
- Understanding these roles can lead to the development of new cancer therapies.
- Further research into ARS-MSC components offers promising avenues for oncology.
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