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A RanGTP-independent Mechanism Allows Ribosomal Protein Nuclear Import for Ribosome Assembly


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Date

2014-08

Publication Type

Journal Article

ETH Bibliography

yes

Citations

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Data

Abstract

Within a single generation time a growing yeast cell imports ∼14 million ribosomal proteins (r-proteins) into the nucleus for ribosome production. After import, it is unclear how these intrinsically unstable and aggregation-prone proteins are targeted to the ribosome assembly site in the nucleolus. Here, we report the discovery of a conserved nuclear carrier Tsr2 that coordinates transfer of the r-protein eS26 to the earliest assembling pre-ribosome, the 90S. In vitro studies revealed that Tsr2 efficiently dissociates importin:eS26 complexes via an atypical RanGTP-independent mechanism that terminates the import process. Subsequently, Tsr2 binds the released eS26, shields it from proteolysis, and ensures its safe delivery to the 90S pre-ribosome. We anticipate similar carriers—termed here escortins—to securely connect the nuclear import machinery with pathways that deposit r-proteins onto developing pre-ribosomal particles.

Publication status

published

Editor

Book title

Journal / series

Volume

3

Pages / Article No.

Publisher

eLife Sciences Publications

Event

Edition / version

Methods

Software

Geographic location

Date collected

Date created

Subject

Organisational unit

03884 - Panse, Vikram G. (SNF-Professur) (ehem.) check_circle

Notes

Funding

260676 - Dissecting the biogenesis of eukaryotic ribosomal subunits (EC)

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