Evidence map›Paper›PMID 35189816›Full record

ArticleBMC molecular and cell biology2022

Exportin Crm1 is important for Swi6 nuclear shuttling and MBF transcription activation in Saccharomyces cerevisiae.

Kenneth D Belanger, William T Yewdell, Matthew F Barber, Amy N Russo, Mark A Pettit, Emily K Damuth, Naveen Hussain, Susan J Geier, Karyn G Belanger

Open access · goldAbstract read
In one paragraph

Article in BMC molecular and cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 50% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Kenneth D BelangerDepartment of Biology, Colgate University, Hamilton, NY, USA. kbelanger@colgate.edu.
William T YewdellDepartment of Biology, Colgate University, Hamilton, NY, USA.
Matthew F BarberDepartment of Biology, Colgate University, Hamilton, NY, USA.
Amy N RussoDepartment of Biology, Colgate University, Hamilton, NY, USA.
Mark A PettitDepartment of Biology, Colgate University, Hamilton, NY, USA.
Emily K DamuthDepartment of Biology, Colgate University, Hamilton, NY, USA.
Naveen HussainDepartment of Biology, Colgate University, Hamilton, NY, USA.
Susan J GeierDepartment of Biology, Colgate University, Hamilton, NY, USA.
Karyn G BelangerDepartment of Biology, Colgate University, Hamilton, NY, USA.
Colgate University · USUniversity of Oregon · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSwi6 acts as a transcription factor in budding yeast, functioning in two different heterodimeric complexes, SBF and MBF, that activate the expression of distinct but overlapping sets of genes. Swi6 undergoes regulated changes in nucleocytoplasmic localization throughout the cell cycle that correlate with changes in gene expression. This study investigates how nucleocytoplasmic transport by multiple transport factors may influence specific Swi6 activities.

resultsHere we show that the exportin Crm1 is important for Swi6 nuclear export and activity. Loss of a putative Crm1 NES or inhibition of Crm1 activity results in changes in nucleocytoplasmic Swi6 localization. Alteration of the Crm1 NES in Swi6 results in decreased MBF-mediated gene expression, but does not affect SBF reporter expression, suggesting that export of Swi6 by Crm1 regulates a subset of Swi6 transcription activation activity. Finally, alteration of the putative Crm1 NES in Swi6 results in cells that are larger than wild type, and this increase in cell size is exacerbated by deletion of Msn5.

conclusionsThese data provide evidence that Swi6 has at least two different exportins, Crm1 and Msn5, each of which interacts with a distinct nuclear export signal. We identify a putative nuclear export signal for Crm1 within Swi6, and observe that export by Crm1 or Msn5 independently influences Swi6-regulated expression of a different subset of Swi6-controlled genes. These findings provide new insights into the complex regulation of Swi6 transcription activation activity and the role of nucleocytoplasmic shuttling in regulated gene expression.

Indexed as

KaryopherinsSaccharomyces cerevisiae ProteinsActive Transport, Cell NucleusCell NucleusExportin 1 ProteinReceptors, Cytoplasmic and NuclearSaccharomyces cerevisiaeTranscriptional ActivationExportin 1 ProteinKaryopherinsMSN5 protein, S cerevisiaeReceptors, Cytoplasmic and NuclearSaccharomyces cerevisiae ProteinsExportinKaryopherinNuclear shuttlingNucleocytoplasmic transportSwi6

Identifiers

PMID35189816
PMCPMC8862259
OpenAlexW4212932070

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.