Mutations in cyr1 and pat1 reveal pheromone-induced G1 arrest in the fission yeast Schizosaccharomyces pombe

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Standard

Mutations in cyr1 and pat1 reveal pheromone-induced G1 arrest in the fission yeast Schizosaccharomyces pombe. / Davey, William John; Nielsen, O; Nielsen, Olaf.

I: Current Genetics, Bind 26, Nr. 2, 01.08.1994, s. 105-12.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Davey, WJ, Nielsen, O & Nielsen, O 1994, 'Mutations in cyr1 and pat1 reveal pheromone-induced G1 arrest in the fission yeast Schizosaccharomyces pombe', Current Genetics, bind 26, nr. 2, s. 105-12.

APA

Davey, W. J., Nielsen, O., & Nielsen, O. (1994). Mutations in cyr1 and pat1 reveal pheromone-induced G1 arrest in the fission yeast Schizosaccharomyces pombe. Current Genetics, 26(2), 105-12.

Vancouver

Davey WJ, Nielsen O, Nielsen O. Mutations in cyr1 and pat1 reveal pheromone-induced G1 arrest in the fission yeast Schizosaccharomyces pombe. Current Genetics. 1994 aug. 1;26(2):105-12.

Author

Davey, William John ; Nielsen, O ; Nielsen, Olaf. / Mutations in cyr1 and pat1 reveal pheromone-induced G1 arrest in the fission yeast Schizosaccharomyces pombe. I: Current Genetics. 1994 ; Bind 26, Nr. 2. s. 105-12.

Bibtex

@article{b5d9c819070a4b109eeed4ae23ac43d4,
title = "Mutations in cyr1 and pat1 reveal pheromone-induced G1 arrest in the fission yeast Schizosaccharomyces pombe",
abstract = "Investigations into sexual differentiation and pheromone response in the fission yeast Schizosaccharomyces pombe are complicated by the need to first starve the cells of nitrogen. Most mating-related experiments are therefore performed on non-dividing cells. Here we overcome this problem by using two mutants that bypass the nutritional requirements and respond to the M-factor mating pheromone in rich medium. The first mutant lacks the cyr1 gene which encodes adenylate cyclase and these cells contain no measurable amounts of cAMP. When M-factor is added to a growing h+ cyr1- strain it causes a transient G1 arrest of cell division, transcription of mat1-Pm, and elongation of the cells to form shmoos. The second mutant contains the temperature-sensitive pat1-114 allele. At 30 degrees C this mutant was previously shown not only to bypass the nutritional signal but also to stop growing in a state derepressed for pheromone-controlled functions. We now report that an h+ pat1-114 strain growing mitotically at 23 degrees C responds to M-factor. This shows that the pat1 protein kinase can be tuned to derepress nutritional signalling while repressing the other stages in the differentiation process.",
keywords = "Adenylate Cyclase, Cell Division, Crosses, Genetic, G1 Phase, Genes, Fungal, Kinetics, Mutagenesis, Peptides, Pheromones, Schizosaccharomyces, Time Factors, Transcription, Genetic",
author = "Davey, {William John} and O Nielsen and Olaf Nielsen",
year = "1994",
month = aug,
day = "1",
language = "English",
volume = "26",
pages = "105--12",
journal = "Current Genetics",
issn = "0172-8083",
publisher = "Springer",
number = "2",

}

RIS

TY - JOUR

T1 - Mutations in cyr1 and pat1 reveal pheromone-induced G1 arrest in the fission yeast Schizosaccharomyces pombe

AU - Davey, William John

AU - Nielsen, O

AU - Nielsen, Olaf

PY - 1994/8/1

Y1 - 1994/8/1

N2 - Investigations into sexual differentiation and pheromone response in the fission yeast Schizosaccharomyces pombe are complicated by the need to first starve the cells of nitrogen. Most mating-related experiments are therefore performed on non-dividing cells. Here we overcome this problem by using two mutants that bypass the nutritional requirements and respond to the M-factor mating pheromone in rich medium. The first mutant lacks the cyr1 gene which encodes adenylate cyclase and these cells contain no measurable amounts of cAMP. When M-factor is added to a growing h+ cyr1- strain it causes a transient G1 arrest of cell division, transcription of mat1-Pm, and elongation of the cells to form shmoos. The second mutant contains the temperature-sensitive pat1-114 allele. At 30 degrees C this mutant was previously shown not only to bypass the nutritional signal but also to stop growing in a state derepressed for pheromone-controlled functions. We now report that an h+ pat1-114 strain growing mitotically at 23 degrees C responds to M-factor. This shows that the pat1 protein kinase can be tuned to derepress nutritional signalling while repressing the other stages in the differentiation process.

AB - Investigations into sexual differentiation and pheromone response in the fission yeast Schizosaccharomyces pombe are complicated by the need to first starve the cells of nitrogen. Most mating-related experiments are therefore performed on non-dividing cells. Here we overcome this problem by using two mutants that bypass the nutritional requirements and respond to the M-factor mating pheromone in rich medium. The first mutant lacks the cyr1 gene which encodes adenylate cyclase and these cells contain no measurable amounts of cAMP. When M-factor is added to a growing h+ cyr1- strain it causes a transient G1 arrest of cell division, transcription of mat1-Pm, and elongation of the cells to form shmoos. The second mutant contains the temperature-sensitive pat1-114 allele. At 30 degrees C this mutant was previously shown not only to bypass the nutritional signal but also to stop growing in a state derepressed for pheromone-controlled functions. We now report that an h+ pat1-114 strain growing mitotically at 23 degrees C responds to M-factor. This shows that the pat1 protein kinase can be tuned to derepress nutritional signalling while repressing the other stages in the differentiation process.

KW - Adenylate Cyclase

KW - Cell Division

KW - Crosses, Genetic

KW - G1 Phase

KW - Genes, Fungal

KW - Kinetics

KW - Mutagenesis

KW - Peptides

KW - Pheromones

KW - Schizosaccharomyces

KW - Time Factors

KW - Transcription, Genetic

M3 - Journal article

C2 - 8001162

VL - 26

SP - 105

EP - 112

JO - Current Genetics

JF - Current Genetics

SN - 0172-8083

IS - 2

ER -

ID: 33577371