Evidence map›Paper›PMID 14718561›Full record

ArticleMolecular biology of the cell2004

The differential roles of budding yeast Tem1p, Cdc15p, and Bub2p protein dynamics in mitotic exit.

Jeffrey N Molk, Scott C Schuyler, Jenny Y Liu, James G Evans, E D Salmon, David Pellman, Kerry Bloom

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

57 citing papers in PubMed, 92 citations in OpenAlex.

  1. Article
  2. A noncanonical GTPase signaling mechanism controls exit from mitosis in budding yeast.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. The signalling lipid PI3,5POpen biology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Budding YeastG3 (Bethesda, Md.) · 2018
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Control of the mitotic exit network during meiosis.Molecular biology of the cell · 2012
    Article
  20. Review
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

7 authors at 3 institutions in 1 country.

Jeffrey N MolkDepartment of Biology, University of North Carolina, Chapel Hill, North Carolina 27599, USA.
Scott C Schuyler
Jenny Y Liu
James G Evans
E D Salmon
David Pellman
Kerry Bloom
Harvard University · USUniversity of North Carolina at Chapel Hill · USWhitehead Institute for Biomedical Research · US

Funding

Structure and Function of a Eukaryotic CentromereR01GM032238 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BLOOM, KERRY S · 1985 to 2025
$6.2M
Structure and Function of a Eukaryotic CentromereR37GM032238 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BLOOM, KERRY S, YEH, ELAINE YING · 2011 to 2020
$5.2M
MECHANISMS OF MITOTIC SPINDLE ASSEMBLY AND FUNCTIONR37GM024364 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SALMON, EDWARD D. · 2004 to 2013
$4.1M
CELL POLARITY AND SPINDLE POSITIONR01GM061345 · NIGMS · DANA-FARBER CANCER INSTITUTE · PI PELLMAN, DAVID S · 2000 to 2011
$3.6M
Cell Cycle Control of the CytoskeletonR37GM061345 · NIGMS · DANA-FARBER CANCER INST · PI PELLMAN, DAVID S · 2014 to 2023
$3.4M
MECHANISMS OF MITOTIC SPINDLE ASSEMBLY AND FUNCTIONR01GM024364 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BLOOM, KERRY S, SALMON, EDWARD D. · 1985 to 2018
$3.1M
NIGMS NIH HHS GM-24364NIGMS NIH HHS GM-32238NIGMS NIH HHS GM61345-01NIGMS NIH HHS R01 GM024364NIGMS NIH HHS R01 GM032238NIGMS NIH HHS R01 GM061345NIGMS NIH HHS R37 GM024364NIGMS NIH HHS R37 GM032238NIGMS NIH HHS R37 GM061345
6 · The paper itself

Abstract

In the budding yeast Saccharomyces cerevisiae the mitotic spindle must be positioned along the mother-bud axis to activate the mitotic exit network (MEN) in anaphase. To examine MEN proteins during mitotic exit, we imaged the MEN activators Tem1p and Cdc15p and the MEN regulator Bub2p in vivo. Quantitative live cell fluorescence microscopy demonstrated the spindle pole body that segregated into the daughter cell (dSPB) signaled mitotic exit upon penetration into the bud. Activation of mitotic exit was associated with an increased abundance of Tem1p-GFP and the localization of Cdc15p-GFP on the dSPB. In contrast, Bub2p-GFP fluorescence intensity decreased in mid-to-late anaphase on the dSPB. Therefore, MEN protein localization fluctuates to switch from Bub2p inhibition of mitotic exit to Cdc15p activation of mitotic exit. The mechanism that elevates Tem1p-GFP abundance in anaphase is specific to dSPB penetration into the bud and Dhc1p and Lte1p promote Tem1p-GFP localization. Finally, fluorescence recovery after photobleaching (FRAP) measurements revealed Tem1p-GFP is dynamic at the dSPB in late anaphase. These data suggest spindle pole penetration into the bud activates mitotic exit, resulting in Tem1p and Cdc15p persistence at the dSPB to initiate the MEN signal cascade.

Indexed as

MitosisAnaphaseCell Cycle ProteinsGreen Fluorescent ProteinsGTP-Binding ProteinsGuanine Nucleotide Exchange FactorsImage Processing, Computer-AssistedKineticsLuminescent ProteinsMicroscopy, FluorescenceMonomeric GTP-Binding ProteinsRecombinant Fusion ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSpindle ApparatusTime FactorsBUB2 protein, S cerevisiaeCDC15 proteinCell Cycle ProteinsGreen Fluorescent ProteinsGTP-Binding ProteinsGuanine Nucleotide Exchange FactorsLTE1 protein, S cerevisiaeLuminescent ProteinsMonomeric GTP-Binding ProteinsRecombinant Fusion ProteinsSaccharomyces cerevisiae ProteinsTEM1 protein, S cerevisiae

Identifiers

PMID14718561
PMCPMC379252
OpenAlexW2131266367

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.