Evidence map›Paper›PMID 9813095›Full record

ArticleThe Journal of cell biology1998

The yeast centrin, cdc31p, and the interacting protein kinase, Kic1p, are required for cell integrity.

D S Sullivan, S Biggins, M D Rose

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

33 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. TheCells · 2021
    Review
  5. The sperm centrioles.Molecular and cellular endocrinology · 2020
    Review
  6. Polarity in Ciliate Models: From Cilia to Cell Architecture.Frontiers in cell and developmental biology · 2019
    Review
  7. MST kinases in development and disease.The Journal of cell biology · 2015
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
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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

3 authors at 1 institution in 1 country.

D S SullivanDepartment of Molecular Biology, Princeton University, Princeton, New Jersey 08544-1014, USA.
S Biggins
M D Rose
Princeton University · US

Funding

GENETICS OF THE YEAST MICROTUBULE ORGANIZING CENTERR01GM052526 · NIGMS · PRINCETON UNIVERSITY · PI ROSE, MARK DAVID · 1995 to 2003
$1.0M
SPINDLE POLE BODY DUPLICATION IN S CEREVISIAEF32GM017998 · NIGMS · PRINCETON UNIVERSITY · PI SULLIVAN, DONALD S · 1995 to 1997
–
NIGMS NIH HHS F32 GM017998NIGMS NIH HHS GM17998NIGMS NIH HHS GM52526NIGMS NIH HHS R01 GM052526
6 · The paper itself

Abstract

Cdc31p is the yeast homologue of centrin, a highly conserved calcium-binding protein of the calmodulin superfamily. Previously centrins have been implicated only in microtubule-based processes. To elucidate the functions of yeast centrin, we carried out a two-hybrid screen for Cdc31p-interacting proteins and identified a novel essential protein kinase of 1,080 residues, Kic1p (kinase that interacts with Cdc31p). Kic1p is closely related to S. cerevisiae Ste20p and the p-21- activated kinases (PAKs) found in a wide variety of eukaryotic organisms. Cdc31p physically interacts with Kic1p by two criteria; Cdc31p coprecipitated with GST-Kic1p and it bound to GST-Kic1p in gel overlay assays. Furthermore, GST-Kic1p exhibited in vitro kinase activity that was CDC31-dependent. Although kic1 mutants were not defective for spindle pole body duplication, they exhibited a variety of mutant phenotypes demonstrating that Kic1p is required for cell integrity. We also found that cdc31 mutants, previously identified as defective for spindle pole body duplication, exhibited lysis and morphological defects. The cdc31 kic1 double mutants exhibited a drastic reduction in the range of permissive temperature, resulting in a severe lysis defect. We conclude that Kic1p function is dependent upon Cdc31p both in vivo and in vitro. We postulate that Cdc31p is required both for SPB duplication and for cell integrity/morphogenesis, and that the integrity/morphogenesis function is mediated through the Kic1p protein kinase.

Indexed as

Chromosomal Proteins, Non-HistoneSaccharomyces cerevisiae ProteinsActinsAmino Acid SequenceCalcium-Binding ProteinsCell Cycle ProteinsFungal ProteinsMolecular Sequence DataMorphogenesisMutationNucleic Acid Hybridizationp21-Activated KinasesProtein Serine-Threonine KinasesActinsCalcium-Binding ProteinscaltractinCDC31 protein, S cerevisiaeCell Cycle ProteinsChromosomal Proteins, Non-HistoneFungal Proteinsp21-Activated KinasesProtein Serine-Threonine KinasesSaccharomyces cerevisiae Proteins

Identifiers

PMID9813095
PMCPMC2148137
OpenAlexW2113085291

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.