Nucleolar structure and function under clinorotation.

M A Sobol

Home/Archive/PubMed

PubMed · 12638617

Nucleolar structure and function under clinorotation.

M A Sobol

View original source ↗Export metadata ↓

Abstract

A nucleolus is the dynamic part of a cell nucleus where rDNA transcription, rRNA precursor processing and transport are proceeding. Investigations of the influence of microgravity and clinorotation on the structure and function of nucleolus began more than thirty years ago but, unfortunately, now there are only some articles concerning the nucleolar peculiarities in altered gravity. Available data about alterations of nucleolar morphology and function under the influence of high and low temperature, hypoxia and UV-microbeam irradiation allow us to put intent attention to the study of the nucleolus reactions on clinorotation. Therefore, the aim of our work was to investigate the ultrastructural organization and functional activity of nucleoli in Lepidium sativum root meristematic cells under clinorotation in order to understand whether a nucleolus can react to gravity.

Explore related subjects

Cell Nucleolus Cell Nucleus Chromatin Gravity, Altered Lepidium sativum Meristem Microscopy, Electron Plant Roots Rotation Vacuoles Weightlessness Simulation Journal Article

Keep this discovery

Explore connections, maps & timelines

BibTeX RIS

M A Sobol. 2001. Nucleolar structure and function under clinorotation.. https://pubmed.ncbi.nlm.nih.gov/12638617/

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

PubMed2026

A nucleolar stress gene signature enables quantitative scoring across multi-omics contexts.

The nucleolus is essential for ribosome biogenesis and cellular homeostasis, and its dysfunction can induce nucleolar stress, a process implicated in cancer and other diseases. However, nucleolar stress is commonly inferred from morphological changes or a limited set of functional assays, and quantitative approaches based on gene expression profiles remain lacking. Here, we integrate literature curation with multi-dataset screening to define a nucleolar stress gene signature and develop a nucleolar stress score (NuS) applicable to bulk transcriptomics, single-cell transcriptomics, proteomics, and spatial transcriptomics. Using this framework, we show in colorectal cancer models that oxaliplatin induces nucleolar stress, suppresses nascent rRNA synthesis, and activates p53 signaling, whereas these responses are attenuated in oxaliplatin-resistant cells. Combined with a ribosome biogenesis activity score (RiboSis), NuS captures related but distinct dimensions of nucleolar function and stratifies tumors into functional states associated with clinical outcomes. NuS-based analysis of perturbational transcriptomes further prioritizes compounds with putative nucleolar stress-inducing activity. Collectively, this study provides a quantitative framework for evaluating nucleolar stress and illustrates its applications in disease stratification and drug mechanism discovery.

Cell Nucleolus↗

PubMed2003

P19ARF inhibits the functions of the HPV16 E7 oncoprotein.

The E7 oncoprotein encoded by high-risk types of human papillomavirus (HPV) plays a significant role in the development of HPV-related cancers. E7 is a potent stimulator of S phase and host DNA replication. These functions of E7 are linked to the deregulation of the Rb family of proteins. For example, E7 binds and induces proteolysis of Rb through the ubiquitin-proteasome pathway. Despite advances in our understanding of E7, reagents that inhibit E7 with promise in therapy have not been developed or identified. Here, we provide evidence that the tumor suppressor ARF can inhibit E7. We show that the expression of ARF causes a relocalization of E7 from the nucleoplasm to the nucleolus. Two distinct regions in ARF overlapping with the MDM2-binding sites are necessary for the relocalization of E7. Furthermore, we show that ARF blocks the proteolysis of Rb induced by E7. In addition, ARF expression inhibits DNA replication induced by E7. Although it is not known whether the endogenous ARF, which is expressed at a low level, interferes with E7, our results suggest that ARF is an effective inhibitor of E7. We speculate that ARF or an ARF-derived molecule might have a significant impact in therapy against HPV-related tumors.

Cell Nucleolus↗

PubMed2003

Formation of nuclear stress granules involves HSF2 and coincides with the nucleolar localization of Hsp70.

The heat-shock response is characterized by the activation of heat-shock transcription factor 1 (HSF1), followed by increased expression of heat-shock proteins (Hsps). The stress-induced subnuclear compartmentalization of HSF1 into nuclear stress granules has been suggested to be an important control step in the regulation of stress response and cellular homeostasis in human cells. In this study, we demonstrate that the less-well characterized HSF2 interacts physically with HSF1 and is a novel stress-responsive component of the stress granules. Based on analysis of our deletion mutants, HSF2 influences to the localization of HSF1 in stress granules. Moreover, our results indicate that the stress granules are dynamic structures and suggest that they might be regulated in an Hsp70-dependent manner. The reversible localization of Hsp70 in the nucleoli strictly coincides with the presence of HSF1 in stress granules and is dramatically suppressed in thermotolerant cells. We propose that the regulated subcellular distribution of Hsp70 is an important regulatory mechanism of HSF1-mediated heat shock response.

Cell Nucleolus↗