Evidence map›Paper›PMID 16143104›Full record

ArticleCell2005

The Set1 methyltransferase opposes Ipl1 aurora kinase functions in chromosome segregation.

Ke Zhang, Wenchu Lin, John A Latham, Gary M Riefler, Jill M Schumacher, Clarence Chan, Kelly Tatchell, David H Hawke, Ryuji Kobayashi, Sharon Y R Dent

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

82 citing papers in PubMed, 152 citations in OpenAlex.

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22 more citing papers are in PubMed but not listed here.

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

10 authors at 3 institutions in 1 country.

Ke ZhangProgram in Genes and Development, Department of Biochemistry and Molecular Biology, M.D. Anderson Cancer Center, University of Texas, Houston, Texas 77030, USA.
Wenchu Lin
John A Latham
Gary M Riefler
Jill M Schumacher
Clarence Chan
Kelly Tatchell
David H Hawke
Ryuji Kobayashi
Sharon Y R Dent
The University of Texas MD Anderson Cancer Center · USLouisiana State University Health Sciences Center Shreveport · USThe University of Texas at Austin · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
THE AIR-2 KINASE PATHWAY AND CYTOKINESIS IN C ELEGANSR01GM062181 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SCHUMACHER, JILL M · 2001 to 2009
$2.4M
MOLECULAR BASIS OF DIFFERENTIATION AND DEVELOPMENTT32HD007325 · NICHD · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KLEIN, WILLIAM H. · 1986 to 2011
$2.1M
GENETIC ANALYSIS OF PROTEIN PHOSPHATASE I IN YEASTR01GM047789 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI TATCHELL, KELLY G. · 1992 to 2004
$1.2M
NCI NIH HHS CA16672NCI NIH HHS P30 CA016672NICHD NIH HHS T32 HD007325NICHD NIH HHS T32 HD07325NIGMS NIH HHS R01 GM047789NIGMS NIH HHS R01 GM062181NIGMS NIH HHS R01 GM062181-03NIGMS NIH HHS R01 GM062181-04NIGMS NIH HHS R01 GM062181-05NIGMS NIH HHS R01GM62181
6 · The paper itself

Abstract

A balance in the activities of the Ipl Aurora kinase and the Glc7 phosphatase is essential for normal chromosome segregation in yeast. We report here that this balance is modulated by the Set1 methyltransferase. Deletion of SET1 suppresses chromosome loss in ipl1-2 cells. Conversely, combination of SET1 and GLC7 mutations is lethal. Strikingly, these effects are independent of previously defined functions for Set1 in transcription initiation and histone H3 methylation. We find that Set1 is required for methylation of conserved lysines in a kinetochore protein, Dam1. Biochemical and genetic experiments indicate that Dam1 methylation inhibits Ipl1-mediated phosphorylation of flanking serines. Our studies demonstrate that Set1 has important, unexpected functions in mitosis. Moreover, our findings suggest that antagonism between lysine methylation and serine phosphorylation is a fundamental mechanism for controlling protein function.

Indexed as

Amino Acid SequenceAurora KinasesCell Cycle ProteinsChromosome DeletionChromosome SegregationDNA-Binding ProteinsGene DeletionHistone-Lysine N-MethyltransferaseIntracellular Signaling Peptides and ProteinsMethylationMethyltransferasesMicrotubule-Associated ProteinsMitosisMolecular Sequence DataMutationPhenotypeAurora KinasesCell Cycle ProteinsDAM1 protein, S cerevisiaeDNA-Binding ProteinsHistone-Lysine N-MethyltransferaseIntracellular Signaling Peptides and ProteinsIPL1 protein, S cerevisiaeMethyltransferasesMicrotubule-Associated ProteinsProtein KinasesProtein Serine-Threonine KinasesSaccharomyces cerevisiae ProteinsSET1 protein, S cerevisiaeTranscription Factors

Identifiers

PMID16143104
PMCPMC1794220
OpenAlexW2012079366

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.