Research Topics
| M NishizawaSummaryAffiliation: Keio University Country: Japan Publications
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Detail Information
Publications
The Pho85 kinase, a member of the yeast cyclin-dependent kinase (Cdk) family, has a regulation mechanism different from Cdks functioning throughout the cell cycleM Nishizawa
Department of Microbiology, Keio University School of Medicine, Shinjuku, Tokyo 160 8582, Japan
Genes Cells 4:627-42. 1999..By analysing the genetic and biochemical properties of Pho85p, we studied whether the regulation of Pho85p activity is similar to other cyclin-dependent kinases (Cdks) directly involved in cell cycle regulation...
Mouse cyclin-dependent kinase (Cdk) 5 is a functional homologue of a yeast Cdk, pho85 kinaseM Nishizawa
Department of Microbiology, Keio University School of Medicine, Shinjuku, Tokyo 160 8582, Japan
J Biol Chem 274:33859-62. 1999..Thus mouse Cdk5 is a functional homologue of yeast Pho85 kinase...
Negative regulation of transcription by the yeast global transcription factors, Gal11 and Sin4M Nishizawa
Department of Microbiology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, Tokyo 160 8582, Japan
Yeast 18:1099-110. 2001..Based on these results, possible mechanisms by which a mediator subcomplex regulates transcription is discussed...
Pho85 kinase, a yeast cyclin-dependent kinase, regulates the expression of UGP1 encoding UDP-glucose pyrophosphorylaseM Nishizawa
Department of Microbiology, Keio University School of Medicine, 35 Shinanomachi, Shinjuku, Tokyo 160 8582, Japan
Yeast 18:239-49. 2001..We also found that expression of several Pho85-cyclin genes were altered by the carbon source, the growth phase and Pho85 kinase itself...
Phosphorylation of sic1, a cyclin-dependent kinase (Cdk) inhibitor, by Cdk including Pho85 kinase is required for its prompt degradationM Nishizawa
Department of Microbiology, Keio University School of Medicine, Tokyo 160 8582, Japan
Mol Biol Cell 9:2393-405. 1998..Pho85 and other G1 Cdks appear to phosphorylate Sic1 at different sites in vivo. Thus at least two distinct Cdks can participate in phosphorylation of Sic1 and may therefore regulate progression through G1...
Yeast Gal11 protein mediates the transcriptional activation signal of two different transacting factors, Gal4 and general regulatory factor I/repressor/activator site binding protein 1/translation upstream factorM Nishizawa
Department of Microbiology, Keio University School of Medicine, Tokyo, Japan
Proc Natl Acad Sci U S A 87:5373-7. 1990....
Isolation and characterization of SGE1: a yeast gene that partially suppresses the gal11 mutation in multiple copiesH Amakasu
Department of Microbiology, Keio University School of Medicine, Tokyo, Japan
Genetics 134:675-83. 1993..SGE1-specific mRNA of 1.8 kilonucleotides was detected by Northern analysis along the direction of the open reading frame. The gene mapped near RAD56, at the right end of chromosome 16...
The yeast GAL11 protein is involved in regulation of the structure and the position effect of telomeresY Suzuki
Department of Microbiology, Keio University School of Medicine, Tokyo, Japan
Mol Cell Biol 14:3791-9. 1994....
Purification and characterization of the yeast negative regulatory protein GAL80S J Yun
Laboratory of Molecular Genetics, Keio University School of Medicine, Tokyo, Japan
J Biol Chem 266:693-7. 1991..We have also purified mutant GAL80 proteins encoded by two different alleles of gal80 known to be incapable of inhibiting the function of GAL4. These proteins were, in fact, unable to bind GAL4...
Toward a protein-protein interaction map of the budding yeast: A comprehensive system to examine two-hybrid interactions in all possible combinations between the yeast proteinsT Ito
Human Genome Center, Institute of Medical Science, University of Tokyo, 4 6 1 Shirokanedai, Minato ku, Tokyo 108 8639, Japan
Proc Natl Acad Sci U S A 97:1143-7. 2000..The approach described here thus will provide many leads for integration of various cellular functions and serve as a major driving force in the completion of the protein-protein interaction map...
A set of Hox proteins interact with the Maf oncoprotein to inhibit its DNA binding, transactivation, and transforming activitiesK Kataoka
Department of Virology, Institute of Medical Science, University of Tokyo, 4 6 1 Shirokanedai, Minato ku 108 8639, Tokyo, Japan
J Biol Chem 276:819-26. 2001..These results suggested that the interaction of a set of Hox proteins with Maf family members may interfere not only with their oncogenicity but also with their physiological roles...
Bach proteins belong to a novel family of BTB-basic leucine zipper transcription factors that interact with MafK and regulate transcription through the NF-E2 siteT Oyake
Department of Biochemistry, Tohoku University School of Medicine, Sendai, Japan
Mol Cell Biol 16:6083-95. 1996..The results suggest that members of the Bach family play important roles in coordinating transcription activation and repression by MafK...
Regulation of transcription by dimerization of erythroid factor NF-E2 p45 with small Maf proteinsK Igarashi
Department of Biochemistry, Tohoku University School of Medicine, Sendai, Japan
Nature 367:568-72. 1994....
Activity and expression of murine small Maf family protein MafKK Igarashi
Department of Biochemistry, Tohoku University School of Medicine, Sendai, Japan
J Biol Chem 270:7615-24. 1995..mRNA for MafK is expressed in fractions enriched for hematopoietic stem cells as well as erythroid cells, suggesting that MafK plays an important regulatory role in hematopoiesis...
Cloning and characterization of a novel erythroid cell-derived CNC family transcription factor heterodimerizing with the small Maf family proteinsK Itoh
Department of Biochemistry, Tohoku University School of Medicine, Sendai, Japan
Mol Cell Biol 15:4184-93. 1995..In a transfection assay, ECH transactivates transcription depending on the presence of NF-E2 sites on the reporter gene plasmid. These results indicate that ECH is likely a key regulator of avian erythropoiesis...
Identification of a gene conferring resistance to zinc and cadmium ions in the yeast Saccharomyces cerevisiaeA Kamizono
Biosciences Laboratory, Mitsubishi Kasei Corporation, Yokohama, Japan
Mol Gen Genet 219:161-7. 1989....
Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in AsiaN Maksimova
Yakut Scientific Centre of Russian Academy of Medical Sciences and Government of Republic of Sakha Yakutia, Yakutsk, Russia
J Med Genet 44:772-8. 2007..In total, 43 patients having short stature syndrome in 37 Yakut families with autosomal recessive prenatal and postnatal nonprogressive growth failure and facial dysmorphism but with normal intelligence have been identified...
cDNA cloning, expression and characterization of human prostaglandin F synthaseT Suzuki-Yamamoto
Department of Anatomy and Cell Biology, School of Medicine, The University of Tokushima, Kuramoto, Japan
FEBS Lett 462:335-40. 1999..These results support the notion that human PGFS plays an important role in the pathogenesis of allergic diseases such as asthma...
Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotypeT Takahashi
Department of Neurology, Tohoku University School of Medicine, Sendai, Japan
Neurology 60:1799-804. 2003..This study revealed that the G3370T mutation was associated with milder forms of MM and the G3510A mutation was associated with a more severe form...
Close kinship of human 20alpha-hydroxysteroid dehydrogenase gene with three aldo-keto reductase genesM Nishizawa
Department of Medical Chemistry Department of Obstetrics and Gynecology, Kansai Medical University, 10 15 Fumizono, Moriguchi, Osaka 570 8506, Japan
Genes Cells 5:111-25. 2000..High homology between human 20alpha-HSD [AKR 1C1] cDNA with other AKRs had caused difficulty in gene isolation and expression analysis. Thus, the metabolism of progesterone in the human reproductive system remained unclear...
Keratin attenuates tumor necrosis factor-induced cytotoxicity through association with TRADDH Inada
Division of Biochemistry, Aichi Cancer Center Research Institute, Aichi 464 8681, Japan
J Cell Biol 155:415-26. 2001..These results indicate that K18 may sequester TRADD to attenuate interactions between TRADD and activated TNFR1 and moderate TNF-induced apoptosis in simple epithelial cells...
A large Japanese SPG4 family with a novel insertion mutation of the SPG4 gene: a clinical and genetic studyM Namekawa
Department of Neurology, Jichi Medical School, Tochigi 329-0498, Japan
J Neurol Sci 185:63-8. 2001..Clinically, it is noteworthy that the disease progression in the patients of this family was slow in spite of the late onset, and more than half of the patients showed severe constipation in addition to pure spastic paraplegia...
Molecular cloning and sequencing of cDNA encoding the phosphatidylinositol kinase from rat brainA Yamakawa
Department of Pharmacology, Tokyo Metropolitan Institute of Gerontology, Japan
J Biol Chem 266:17580-3. 1991..The messenger RNA for PI 4-kinase was found predominantly in brain and rat neural cell lines. This PI kinase may play a specific role in neural signal transduction...
Analysis of all exons of TSC1 and TSC2 genes for germline mutations in Japanese patients with tuberous sclerosis: report of 10 mutationsY Yamashita
Department of Experimental Pathology, Cancer Institute, Tokyo, Japan
Am J Med Genet 90:123-6. 2000..e., (1) TSC1 mutations are rarer in sporadic cases than in familial cases, (2) substantial numbers of sporadic cases arise from mutations in the TSC2 gene, and (3) mutations of the TSC1 gene may cause premature truncation of hamartin...
Regulation of lens fiber cell differentiation by transcription factor c-MafS Kawauchi
Center for Tsukuba Advanced Research Alliance and Institute of Basic Medical Sciences, University of Tsukuba, Tsukuba 305 8577, Japan
J Biol Chem 274:19254-60. 1999..The expression of crystallin genes was severely impaired in the c-maf-null mutant mouse lens. These results demonstrate that c-Maf is an indispensable regulator of lens differentiation during murine development...
Molecular cloning of cDNA and a chromosomal gene encoding GPE1-BP, a nuclear protein which binds to granulocyte colony-stimulating factor promoter element 1M Nishizawa
Osaka Bioscience Institute, Japan
FEBS Lett 282:95-7. 1991..The nuclear extract from COS cells transfected with the cDNA showed GPE1-binding activity. Transcripts were ubiquitously detected, and may be spliced from two exons of a single gene...
Structure, expression, and chromosomal location of the human c-fgr geneM Nishizawa
Mol Cell Biol 6:511-7. 1986..Furthermore, karyotype analysis of several human-mouse hybrid cells and Southern blot analyses of DNAs of the hybrids with a human c-fgr locus-specific probe showed that this gene is located on chromosome 1...
cDNA structure, alternative splicing and exon-intron organization of the predisposing tuberous sclerosis (Tsc2) gene of the Eker rat modelT Kobayashi
Department of Experimental Pathology, Cancer Institute, Tokyo, Japan
Nucleic Acids Res 23:2608-13. 1995....
Small Maf proteins heterodimerize with Fos and may act as competitive repressors of the NF-E2 transcription factorK Kataoka
Department of Viral Oncology, Cancer Institute, Tokyo, Japan
Mol Cell Biol 15:2180-90. 1995..These results raise the possibility that tissue-specific gene expression and differentiation of erythroid cells are regulated by competition among Fos, NF-E2 p45, and Ech for small Maf proteins and for binding sites...
MafB, a new Maf family transcription activator that can associate with Maf and Fos but not with JunK Kataoka
Department of Viral Oncology, Cancer Institute, Tokyo, Japan
Mol Cell Biol 14:7581-91. 1994..Through formation of numerous bZip dimers, the Maf family proteins along with the AP-1 components should provide great diversity in transcriptional regulation for a wide variety of genes...
Molecular cloning of the aminopeptidase Y gene of Saccharomyces cerevisiae. Sequence analysis and gene disruption of a new aminopeptidaseM Nishizawa
Meiji Institute of Health Science, Odawara, Japan
J Biol Chem 269:13651-5. 1994..2 and 2.8%, respectively. Mutant cells showed no ability to hydrolyze Lys-Ala-MCA to Lys and Ala-MCA, although vacuolar carboxypeptidase Y activity was similar to that in wild-type cells...
Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferaseO Koiwai
Laboratories of Biochemistry, Aichi Cancer Center Research Institute, Nagoya, Japan
Hum Mol Genet 4:1183-6. 1995..However, the UGT activity of the patient with Gilbert's syndrome was unexpectedly < 50% of the normal, perhaps as the result of the dominant negative nature of the mutation...
A novel two-base mutation in the Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis in JapanM Morita
Department of Neurology, Tohoku University School of Medicine, Japan
Neurosci Lett 205:79-82. 1996..These findings suggest that clinical courses are variable with each mutation, even in the same exon...
Small Maf proteins interact with the human transcription factor TCF11/Nrf1/LCR-F1O Johnsen
Biotechnology Centre of Oslo, University of Oslo, Norway
Nucleic Acids Res 24:4289-97. 1996..These findings place TCF11 as a good candidate for the proposed widely expressed factor(s) known to interact with small Maf proteins and bind NF-E2 sites in a sequence-specific manner resembling NF-E2...
Single sperm analysis of the CAG repeats in the gene for dentatorubral-pallidoluysian atrophy (DRPLA): the instability of the CAG repeats in the DRPLA gene is prominent among the CAG repeat diseasesY Takiyama
Department of Neurology, Jichi Medical School, 3311 1 Minamikawachi, Kawachi, Tochigi 329 0498, Japan
Hum Mol Genet 8:453-7. 1999..161) from the expected 1:1 segregation ratio, and thus segregation distortion of expanded alleles in meiosis in male patients with DRPLA was not demonstrated...
Total deletion and a missense mutation of ITPR1 in Japanese SCA15 familiesK Hara
Department of Molecular Neuroscience, Center for Bioresource based Researches, Brain Research Institute, Niigata University, 1 757, Asahi machi dori, Niigata City 951 8585, Japan
Neurology 71:547-51. 2008..Recently, partial deletions involving both the type 1 inositol 1,4,5-triphosphate receptor (ITPR1) and sulfatase modifying factor 1 (SUMF1) genes have been identified in Australian and British families with SCA15...
