Abstract

The nucleolus, the ribosomal factory of the cell, has emerged as a key player that regulates many aspects of cell biology. Several thousand proteins associate at least transiently with nucleoli, thereby generating a highly dynamic compartment with a protein profile which is sensitive to changes in cell physiology and pharmacological agents. Powerful tools that reliably demarcate the nucleoli are a prerequisite to measure their composition and activities. Previously, we developed quantitative methods to measure fluorescently labeled molecules in nucleoli. While these tools identify nucleoli under control and mild stress conditions, the accurate detection of nucleolar boundaries under harsh experimental conditions is complicated by the lack of appropriate markers for the nucleolar compartment. Using fluorescence microscopy we have now identified new marker proteins to detect nucleoli upon (a) severe stress and (b) drug treatments that trigger a pronounced reorganization of nucleoli. Our results demonstrate that nucleolin is an ideal marker to delimit nucleoli when cells are exposed to heat or oxidative stress. Furthermore, we show for the first time that cellular apoptosis susceptibility protein (CAS) and human antigen R protein (HuR) are excluded from nucleoli and can be employed to delimit these compartments under severe conditions that redistribute major nucleolar proteins. As proof-of-principle, we used these markers to demarcate nucleoli in cells treated with pharmacological compounds that disrupt the nucleolar organization. Furthermore, to gain new insights into the biology of the nucleolus, we applied our protocols and quantified stress- and drug-induced changes in nucleolar organization and function. Finally, we show that CAS, HuR and nucleolin not only identify nucleoli in optical sections, but are also suitable to demarcate the nucleolar border following 3D reconstruction. Taken together, our studies present novel marker proteins that delimit nucleoli with high confidence under a variety of experimental settings.

Highlights

  • The nucleolus is a specialized compartment in the nucleus that serves as the site for ribosome biogenesis [1]

  • Our results demonstrate that nucleolin, cellular apoptosis susceptibility protein (CAS) and human antigen R protein (HuR) can be employed to identify nucleoli in different cell types under harsh experimental conditions that alter the organization and function of this subnuclear compartment

  • The combination of DAPI and RNA pol II images improved the correct identification of nucleoli, this protocol requires a large number of processing steps and complicates image analyses

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Summary

Introduction

The nucleolus is a specialized compartment in the nucleus that serves as the site for ribosome biogenesis [1]. Nucleoli are assembled around chromosomal regions that contain tandem repeats of rDNA genes. These genes code for 45S pre-rRNA which is processed into 28S, 18S and 5.8S rRNAs [1,2]. Processing of the 45S precursor relies on numerous factors and is a pre-requisite for the proper assembly of ribosomal subunits [3]. Aside from the assembly of ribosomal subunits, the nucleolus is implicated in a wide array of additional cellular functions. The nucleolus is organized as a tripartite compartment that contains fibrillar centers, dense fibrillar components and the granular component [1,2]

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