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Mek1 kinase activity functions downstream of RED1 in the regulation of meiotic double strand break repair in budding yeast
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
14595109
retrieved
1 December 2016
title
Mek1 kinase activity functions downstream of RED1 in the regulation of meiotic double strand break repair in budding yeast
(English)
1 reference
stated in
PubMed
PubMed ID
14595109
retrieved
1 December 2016
main subject
cell biology
0 references
Red1p YLR263W
1 reference
stated in
GOA release 2020-03-11
author name string
Lihong Wan
series ordinal
1
0 references
Teresa de los Santos
series ordinal
2
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Chao Zhang
series ordinal
3
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Kevan Shokat
series ordinal
4
0 references
Nancy M Hollingsworth
series ordinal
5
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language of work or name
English
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publication date
January 2004
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published in
Molecular Biology of the Cell
1 reference
stated in
PubMed
PubMed ID
14595109
retrieved
1 December 2016
volume
15
0 references
issue
1
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page(s)
11-23
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cites work
Mutant tyrosine kinases with unnatural nucleotide specificity retain the structure and phospho-acceptor specificity of the wild-type enzyme
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Bypass of a meiotic checkpoint by overproduction of meiotic chromosomal proteins
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Pachytene exit controlled by reversal of Mek1-dependent phosphorylation
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Genetic control of recombination partner preference in yeast meiosis. Isolation and characterization of mutants elevated for meiotic unequal sister-chromatid recombination.
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Yeast Rad54 promotes Rad51-dependent homologous DNA pairing via ATP hydrolysis-driven change in DNA double helix conformation.
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Red1p, a MEK1-dependent phosphoprotein that physically interacts with Hop1p during meiosis in yeast
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Synaptonemal complex morphogenesis and sister-chromatid cohesion require Mek1-dependent phosphorylation of a meiotic chromosomal protein
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20 March 2017
Interhomolog bias during meiotic recombination: meiotic functions promote a highly differentiated interhomolog-only pathway
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The yeast Red1 protein localizes to the cores of meiotic chromosomes
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Members of the NAP/SET family of proteins interact specifically with B-type cyclins
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RecA homologs Dmc1 and Rad51 interact to form multiple nuclear complexes prior to meiotic chromosome synapsis.
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A meiosis-specific protein kinase homolog required for chromosome synapsis and recombination
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20 March 2017
DMC1: a meiosis-specific yeast homolog of E. coli recA required for recombination, synaptonemal complex formation, and cell cycle progression
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A coiled-coil related protein specific for synapsed regions of meiotic prophase chromosomes
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20 March 2017
Differential timing and control of noncrossover and crossover recombination during meiosis
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PubMed Central
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20 March 2017
Role of RAD52 epistasis group genes in homologous recombination and double-strand break repair
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Mechanism and control of meiotic recombination initiation
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7 April 2017
The single-end invasion: an asymmetric intermediate at the double-strand break to double-holliday junction transition of meiotic recombination
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7 April 2017
Active and inactive protein kinases: structural basis for regulation
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PubMed Central
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7 April 2017
ZIP1 is a synaptonemal complex protein required for meiotic chromosome synapsis
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7 April 2017
The FHA domain
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PubMed Central
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29 September 2017
Replication protein A is sequentially phosphorylated during meiosis
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PubMed Central
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29 September 2017
Magic bullets for protein kinases
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PubMed Central
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29 September 2017
The Rad51 and Dmc1 recombinases: a non-identical twin relationship
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29 September 2017
The pachytene checkpoint
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PubMed Central
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29 September 2017
Meiotic segregation, synapsis, and recombination checkpoint functions require physical interaction between the chromosomal proteins Red1p and Hop1p
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PubMed Central
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29 September 2017
Yeast meiosis-specific protein Hop1 binds to G4 DNA and promotes its formation
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PubMed Central
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29 September 2017
High copy number suppression of the meiotic arrest caused by a dmc1 mutation: REC114 imposes an early recombination block and RAD54 promotes a DMC1-independent DSB repair pathway.
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PubMed Central
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29 September 2017
The FHA domain is a modular phosphopeptide recognition motif.
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307523
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29 September 2017
DNA-binding activities of Hop1 protein, a synaptonemal complex component from Saccharomyces cerevisiae
1 reference
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PubMed Central
reference URL
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29 September 2017
Genetic interactions between HOP1, RED1 and MEK1 suggest that MEK1 regulates assembly of axial element components during meiosis in the yeast Saccharomyces cerevisiae
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307523
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29 September 2017
A conditional allele of the Saccharomyces cerevisiae HOP1 gene is suppressed by overexpression of two other meiosis-specific genes: RED1 and REC104.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307523
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29 September 2017
HOP1: a yeast meiotic pairing gene
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stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307523
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29 September 2017
The MRE4 gene encodes a novel protein kinase homologue required for meiotic recombination in Saccharomyces cerevisiae
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307523
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29 September 2017
Meiotic induction of the yeast HOP1 gene is controlled by positive and negative regulatory sites
1 reference
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PubMed Central
reference URL
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29 September 2017
A chemical genetic screen for direct v-Src substrates reveals ordered assembly of a retrograde signaling pathway
1 reference
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PubMed Central
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2 June 2018
Sister chromatid-based DNA repair is mediated by RAD54, not by DMC1 or TID1.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307523
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2 June 2018
Chiasmata, crossovers, and meiotic chromosome segregation.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307523
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2 June 2018
Meiosis in asynaptic yeast
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307523
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2 June 2018
Targeted stimulation of meiotic recombination.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=307523
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27 November 2018
Meiosis-induced double-strand break sites determined by yeast chromatin structure
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14595109
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Expression and DNA sequence of RED1, a gene required for meiosis I chromosome segregation in yeast
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14595109
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Meiotic gene conversion and crossing over: their relationship to each other and to chromosome synapsis and segregation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14595109
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14595109
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Meiotic cells monitor the status of the interhomolog recombination complex
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14595109
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1091/MBC.E03-07-0499
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1433492
OpenCitations bibliographic resource ID
1433492
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1433492
PMCID
307523
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1433492
PubMed ID
14595109
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1433492
ResearchGate publication ID
9028963
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