The R2TP chaperone complex: its involvement in snoRNP assembly and tumorigenesis
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Published on: May 9, 2020
Abstract:
R2TP was originally identified in yeast Saccharomyces cerevisiae as Hsp90 interacting complex, and is composed of four different proteins: Rvb1, Rvb2, Tah1, and Pih1. This complex is well-conserved in eukaryotes, and is involved in many cellular processes such as snoRNP biogenesis, RNA polymerase assembly, PIKK signaling, and apoptosis. An increasing number of research related to R2TP suggests a linkage of its function with tumorigenesis. In this review, we provide an overview of several recent studies on R2TP that are related to cell proliferation and carcinogenesis, and propose a possible role of R2TP in tumorigenesis through regulating snoRNA/snoRNP biogenesis.
Insights
The R2TP complex, crucial for cellular processes, is increasingly linked to cancer. This review explores its role in cell proliferation and carcinogenesis, proposing a link to tumorigenesis via snoRNA/snoRNP biogenesis regulation.
Area of Science:
- Molecular Biology
- Cell Biology
- Oncology
Background:
- The R2TP complex, initially identified in yeast, comprises Rvb1, Rvb2, Tah1, and Pih1.
- This evolutionarily conserved eukaryotic complex participates in vital cellular functions including snoRNP biogenesis, RNA polymerase assembly, PIKK signaling, and apoptosis.
Purpose of the Study:
- To review recent research linking the R2TP complex to cell proliferation and carcinogenesis.
- To propose a potential mechanism for R2TP's involvement in tumorigenesis through the regulation of snoRNA/snoRNP biogenesis.
Main Methods:
- Literature review of recent studies on the R2TP complex.
- Analysis of the R2TP complex's role in cellular processes relevant to cancer.
Main Results:
- Emerging evidence suggests a connection between R2TP function and tumorigenesis.
- The R2TP complex is implicated in regulating key cellular pathways.
Conclusions:
- The R2TP complex plays a significant role in cellular processes.
- Dysregulation of R2TP may contribute to cancer development by affecting snoRNA/snoRNP biogenesis.
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