Abstract
Fission yeast cold-sensitive mutants nda1-376 and nda4-108 display a cell cycle block phenotype at the restrictive temperature (cell elongation with the single nucleus) accompanied by an alteration in the nuclear chromatin region. DNA content analysis shows that the onset of DNA synthesis is blocked or greatly delayed in both mutant cells, the block being reversible in nda4-108. Upon release to the permissive temperature, nda4-108 cells resumed replicating DNA, followed by mitosis and cytokinesis. The nda4 phenotype was partly rescued by the addition of Ca2+ to the medium; Ca2+ plays a positive role in the nda4+ function. The predicted protein sequences of nda1+ and nda4+ isolated by complementation are similar to each other and also, respectively, to those of the budding yeast, MCM2 and CDC46, both of which are members of the gene family required for the initiation of DNA replication. The central domains of these proteins are conserved, whereas the NH2- and COOH- domains are distinct. Results of the disruption of the nda1+ and nda4+ genes demonstrates that they are essential for viability.
MeSH Terms
Amino Acid Sequence
Antigens, CD/genetics
Base Sequence
Calcium/pharmacology
Cell Cycle Proteins
Cell Division/genetics
Chromatin/physiology
Chromosome Mapping
Chromosomes, Fungal
Cloning, Molecular
DNA, Fungal/biosynthesis,isolation & purification
DNA-Binding Proteins
Fungal Proteins/chemistry,genetics
Genes, Fungal/genetics
Genetic Complementation Test
Membrane Cofactor Protein
Membrane Glycoproteins/genetics
Molecular Sequence Data
Mutation
S Phase
Schizosaccharomyces/cytology,genetics,growth & development
Schizosaccharomyces pombe Proteins
Sequence Analysis
Sequence Homology, Amino Acid
Temperature
Transformation, Genetic
Chemicals
Antigens, CD
Cell Cycle Proteins
Chromatin
DNA, Fungal
DNA-Binding Proteins
Fungal Proteins
Membrane Cofactor Protein
Membrane Glycoproteins
Schizosaccharomyces pombe Proteins
mcm5 protein, S pombe
mcm2 protein, S pombe
Calcium
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Miyake S
Laboratory of Molecular Genetics, University of Tokyo, Japan.
Okishio N
Samejima I
Hiraoka Y
Toda T
Saitoh I
Yanagida M
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