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Updated: Jul 17, 2026

Intranuclear Microinjection of DNA into Dissociated Adult Mammalian Neurons
Published on: December 10, 2009
TOR-in(g) the nucleus
Chi Kwan Tsang1, X F Steven Zheng
1Department of Pharmacology and Cancer Institute of New Jersey, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.
Abstract:
Target of rapamycin (TOR) is a central component of the eukaryotic growth regulatory network. TOR controls the expression of diverse genes by all three RNA polymerases, including ribosome biogenesis, utilization and transport of nutrients, and stress-related genes. Until recently, TOR was thought to be a classical signaling kinase that regulates transcription factors in the cytoplasm. However, our recent study shows that in yeast, TOR dynamically shuttles between the cytoplasm and nucleus, and binds to 35S ribosomal DNA (rDNA) promoter. Importantly, nuclear localization and promoter-binding is crucial for TOR to control RNA polymerase (Pol) I-dependent 35S rDNA transcription. In contrast, either cytoplasmic or nuclear TOR is sufficient to regulate Pol II-dependent transcription. These observations suggest that TOR in the nucleus plays an important role in gene regulation, and that TOR takes a multifaceted approach to control expression of different genes.
Insights
The Target of rapamycin (TOR) protein moves between the cytoplasm and nucleus in yeast. Nuclear TOR is essential for regulating ribosomal DNA transcription, highlighting its multifaceted role in gene expression.
Area of Science:
- Molecular Biology
- Cell Biology
- Yeast Genetics
Background:
- The Target of rapamycin (TOR) pathway is a key regulator of eukaryotic cell growth.
- TOR influences gene expression related to ribosome biogenesis, nutrient transport, and stress response.
- Previously, TOR was primarily considered a cytoplasmic signaling kinase.
Purpose of the Study:
- To investigate the subcellular localization and nuclear function of TOR in yeast.
- To determine the role of TOR's nuclear localization in regulating transcription by different RNA polymerases.
- To elucidate the multifaceted mechanisms by which TOR controls gene expression.
Main Methods:
- Yeast genetics and molecular biology techniques.
- Analysis of TOR protein localization using microscopy.
- Assessment of RNA polymerase I and II dependent transcription in yeast mutants.
Main Results:
- TOR dynamically shuttles between the cytoplasm and nucleus in yeast cells.
- Nuclear localization and binding to the 35S ribosomal DNA (rDNA) promoter are critical for TOR's regulation of RNA polymerase I transcription.
- TOR in either the cytoplasm or nucleus is sufficient for regulating RNA polymerase II-dependent transcription.
Conclusions:
- TOR's nuclear localization is crucial for specific gene regulatory functions, particularly for rDNA transcription.
- TOR employs distinct mechanisms to regulate transcription by RNA polymerase I and RNA polymerase II.
- These findings reveal a more complex and multifaceted role for TOR in eukaryotic gene regulation, extending beyond its previously understood cytoplasmic functions.
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