Detection of mRNAs Anchored to the Nuclear Envelope During Export Inhibition in Living Cells

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

1 Scopus citations

Abstract

Export of mRNA transcripts from the cell nucleus is a complex and multistep process, regulated by various proteins and control mechanisms. Recent studies have demonstrated the rapid passage of mRNA–protein complexes (mRNPs) through the nuclear pore complex (NPC) as well as the ability to detect mRNPs stalled at the NPC during inhibition of the mRNA export process. In this chapter, we describe ways to block mRNA export and present an image analysis method to identify mRNPs stuck at the NPC during such blocks. Using the MS2 mRNA-tagging system to track single mRNPs in living cells we are able to examine their intracellular distribution and dynamics both in the nucleoplasm and at the nuclear periphery. We use this method to identify and count the number of static mRNPs anchored to the nuclear envelope under different conditions of mRNA export inhibition.

Original languageEnglish
Title of host publicationMethods in Molecular Biology
PublisherHumana Press Inc.
Pages151-163
Number of pages13
DOIs
StatePublished - 2019

Publication series

NameMethods in Molecular Biology
Volume2038
ISSN (Print)1064-3745
ISSN (Electronic)1940-6029

Bibliographical note

Publisher Copyright:
© Springer Science+Business Media, LLC, part of Springer Nature 2019.

Funding

Y.S.T. is supported by the Israel Science Foundation and Germa-n–Israeli Foundation.

Funders
Israeli Foundation
Israel Science Foundation

    Keywords

    • Gene expression
    • Image processing and analysis
    • Live cell imaging
    • Nuclear pore complex (NPC)
    • Single particle tracking
    • mRNA export
    • mRNP

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