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1.
Mol Cell Biol ; 21(15): 4875-88, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11438645

ABSTRACT

The CBF1 (centromere binding factor 1) gene of Candida glabrata was cloned by functional complementation of the methionine biosynthesis defect of a Saccharomyces cerevisiae cbf1 deletion mutant. The C. glabrata-coded protein, CgCbf1, contains a basic-helix-loop-helix leucine zipper domain and has features similar to those of other budding yeast Cbf1 proteins. CgCbf1p binds in vitro to the centromere DNA element I (CDEI) sequence GTCACATG with high affinity (0.9 x 10(9) M(-1)). Bandshift experiments revealed a pattern of protein-DNA complexes on CgCEN DNA different from that known for S. cerevisiae. We examined the effect of altering the CDEI binding site on CEN plasmid segregation, using a newly developed colony-sectoring assay. Internal deletion of the CDEI binding site led only to a fivefold increase in rates of plasmid loss, indicating that direct binding of Cbf1p to the centromere DNA is not required for full function. Additional deletion of sequences to the left of CDEI, however, led to a 70-fold increase in plasmid loss rates. Deletion of the CBF1 gene proved to be lethal in C. glabrata. C. glabrata cells containing the CBF1 gene under the influence of a shutdown promoter (tetO-ScHOP) arrested their growth after 5 h of cultivation in the presence of the reactive drug doxycycline. DAPI (4',6'-diamidino-2-phenylindole) staining of the arrested cells revealed a significant increase in the number of large-budded cells with single nuclei, 2C DNA content, and short spindles, indicating a defect in the G(2)/M transition of the cell cycle. Thus, we conclude that Cbf1p is required for chromosome segregation in C. glabrata.


Subject(s)
Candida/genetics , Chromosomes/ultrastructure , DNA-Binding Proteins/physiology , Fungal Proteins/physiology , Saccharomyces cerevisiae Proteins , Amino Acid Sequence , Anti-Bacterial Agents/pharmacology , Basic Helix-Loop-Helix Leucine Zipper Transcription Factors , Binding Sites , Candida/metabolism , Centromere/metabolism , Chromatin/metabolism , Chromosome Segregation , Chromosomes/metabolism , Chromosomes/physiology , Cloning, Molecular , DNA/metabolism , Dose-Response Relationship, Drug , Doxycycline/pharmacology , Epitopes , Fluorescent Dyes/pharmacology , Gene Deletion , Genetic Complementation Test , Indoles/pharmacology , Kinetics , Methionine/metabolism , Models, Genetic , Molecular Sequence Data , Mutagenesis , Mutation , Phenotype , Plasmids/metabolism , Precipitin Tests , Promoter Regions, Genetic , Protein Binding , Protein Structure, Tertiary , Recombinant Proteins/metabolism , Saccharomyces cerevisiae/genetics , Sequence Analysis, DNA , Sequence Homology, Amino Acid , Structure-Activity Relationship , Time Factors
2.
Wound Repair Regen ; 9(6): 522-30, 2001.
Article in English | MEDLINE | ID: mdl-11896995

ABSTRACT

The expression of SPARC (secreted protein acidic and rich in cysteine/osteonectin/BM-40) is elevated in endothelial cells participating in angiogenesis in vitro and in vivo. SPARC acts on endothelial cells to elicit changes in cell shape and to inhibit cell cycle progression. In addition, SPARC binds to and diminishes the mitotic activity of vascular endothelial growth factor. To determine the effect(s) of SPARC on angiogenic responses in vivo, we implanted polyvinyl alcohol sponges subcutaneously into wild-type and SPARC-null mice. On days 12 and 20 following implantation, SPARC-null mice showed increased cellular invasion of the sponges in comparison to wild-type mice. Areas of the sponge with the highest cell density exhibited the highest numbers of vascular profiles in both wild-type and SPARC-null animals. The endothelial component of the vessels was substantiated by immunoreactivity with three different markers specific for endothelial cells. Although sponges from SPARC-null relative to wild-type mice were populated by significantly more cells and blood vessels, an increase in the ratio of vascular to nonvascular cells was not apparent. No differences in the percentage of proliferating cells within the sponge were detected between wild-type and SPARC-null sections. However, elevated levels of vascular endothelial growth factor were associated with sponges from SPARC-null versus wild-type mice. An increase in vascular endothelial growth factor production was also observed in SPARC-null primary dermal fibroblasts relative to those of wild-type cells. In conclusion, we have shown that the fibrovascular invasion of polyvinyl alcohol sponges is enhanced in mice lacking SPARC, and we propose that increased levels of vascular endothelial growth factor account, at least in part, for this response.


Subject(s)
Neovascularization, Physiologic/physiology , Osteonectin/physiology , Animals , Endothelial Growth Factors/metabolism , Fibroblasts/metabolism , Immunohistochemistry , Lymphokines/metabolism , Mice , Mice, Inbred C57BL , Mice, Inbred Strains , Polyvinyl Alcohol/administration & dosage , Skin/cytology , Vascular Endothelial Growth Factor A , Vascular Endothelial Growth Factors
3.
Proc Natl Acad Sci U S A ; 96(23): 13208-13, 1999 Nov 09.
Article in English | MEDLINE | ID: mdl-10557299

ABSTRACT

Yeast two-hybrid and genetic interaction screens indicate that Bir1p, a yeast protein containing phylogenetically conserved antiapoptotic repeat domains called baculovirus inhibitor of apoptosis repeats (BIRs), is involved in chromosome segregation events. In the two-hybrid screen, Bir1p specifically interacts with Ndc10p, an essential component of the yeast kinetochore. Although Bir1p carries two BIR motifs in the N-terminal region, the C-terminal third of the protein is sufficient to provide strong interaction with Ndc10p and moderate interaction with Skp1p, another essential component of the yeast kinetochore. In addition, deletion of BIR1 is synthetically lethal with deletion of CBF1 or CTF19, genes specifying two other components of the yeast kinetochore. Yeast cells deleted of BIR1 have a chromosome-loss phenotype, which can be completely rescued by elevating NDC10 dosage. Furthermore, overexpression of either full-length or the C-terminal region of Bir1p can efficiently suppress the chromosome-loss phenotype of both bir1Delta null and skp1-4 mutants. Our data suggest that Bir1p participates in chromosome segregation events, either directly or via interaction with kinetochore proteins, and these effects are apparently not mediated by the BIR domains of Bir1p.


Subject(s)
Apoptosis/physiology , Chromosomes, Fungal , Potassium Channels/physiology , Saccharomyces cerevisiae Proteins , Saccharomyces cerevisiae/genetics , Base Sequence , DNA Primers , DNA-Binding Proteins/metabolism , Fungal Proteins/metabolism , Genes, Fungal , Genes, Lethal , Kinetochores , Phenotype , Potassium Channels/metabolism
4.
Mol Cell Biol ; 19(11): 7461-72, 1999 Nov.
Article in English | MEDLINE | ID: mdl-10523634

ABSTRACT

In budding yeast (Saccharomyces cerevisiae), the majority of box H/ACA small nucleolar RNPs (snoRNPs) have been shown to direct site-specific pseudouridylation of rRNA. Among the known protein components of H/ACA snoRNPs, the essential nucleolar protein Cbf5p is the most likely pseudouridine (Psi) synthase. Cbf5p has considerable sequence similarity to Escherichia coli TruBp, a known Psi synthase, and shares the "KP" and "XLD" conserved sequence motifs found in the catalytic domains of three distinct families of known and putative Psi synthases. To gain additional evidence on the role of Cbf5p in rRNA biosynthesis, we have used in vitro mutagenesis techniques to introduce various alanine substitutions into the putative Psi synthase domain of Cbf5p. Yeast strains expressing these mutated cbf5 genes in a cbf5Delta null background are viable at 25 degrees C but display pronounced cold- and heat-sensitive growth phenotypes. Most of the mutants contain reduced levels of Psi in rRNA at extreme temperatures. Substitution of alanine for an aspartic acid residue in the conserved XLD motif of Cbf5p (mutant cbf5D95A) abolishes in vivo pseudouridylation of rRNA. Some of the mutants are temperature sensitive both for growth and for formation of Psi in the rRNA. In most cases, the impaired growth phenotypes are not relieved by transcription of the rRNA from a polymerase II-driven promoter, indicating the absence of polymerase I-related transcriptional defects. There is little or no abnormal accumulation of pre-rRNAs in these mutants, although preferential inhibition of 18S rRNA synthesis is seen in mutant cbf5D95A, which lacks Psi in rRNA. A subset of mutations in the Psi synthase domain impairs association of the altered Cbf5p proteins with selected box H/ACA snoRNAs, suggesting that the functional catalytic domain is essential for that interaction. Our results provide additional evidence that Cbf5p is the Psi synthase component of box H/ACA snoRNPs and suggest that the pseudouridylation of rRNA, although not absolutely required for cell survival, is essential for the formation of fully functional ribosomes.


Subject(s)
Microtubule-Associated Proteins/genetics , Point Mutation , RNA Processing, Post-Transcriptional , RNA, Ribosomal/metabolism , RNA-Binding Proteins/genetics , Ribonucleoproteins, Small Nuclear , Saccharomyces cerevisiae Proteins , Uridine Monophosphate/biosynthesis , Amino Acid Sequence , Conserved Sequence , Hydro-Lyases/metabolism , Molecular Sequence Data , RNA Polymerase II/metabolism , RNA Precursors/metabolism , Ribonucleoproteins, Small Nucleolar/metabolism , Ribosomes/metabolism , Saccharomyces cerevisiae , Transcription, Genetic
5.
J Cell Biol ; 146(2): 415-25, 1999 Jul 26.
Article in English | MEDLINE | ID: mdl-10427094

ABSTRACT

We have identified a novel centromere-associated gene product from Saccharomyces cerevisiae that plays a role in spindle assembly and stability. Strains with a deletion of SLK19 (synthetic lethal Kar3p gene) exhibit abnormally short mitotic spindles, increased numbers of astral microtubules, and require the presence of the kinesin motor Kar3p for viability. When cells are deprived of both Slk19p and Kar3p, rapid spindle breakdown and mitotic arrest is observed. A functional fusion of Slk19p to green fluorescent protein (GFP) localizes to kinetochores and, during anaphase, to the spindle midzone, whereas Kar3p-GFP was found at the nuclear side of the spindle pole body. Thus, these proteins seem to play overlapping roles in stabilizing spindle structure while acting from opposite ends of the microtubules.


Subject(s)
Centromere/metabolism , Fungal Proteins/metabolism , Saccharomyces cerevisiae Proteins , Saccharomyces cerevisiae/cytology , Spindle Apparatus/metabolism , Anaphase , Cell Nucleus/metabolism , Cytoplasm/metabolism , Fungal Proteins/genetics , Genes, Lethal , Kinesins , Kinetochores/metabolism , Microscopy, Fluorescence , Microtubule-Associated Proteins/genetics , Microtubule-Associated Proteins/metabolism , Microtubules/metabolism , Mitosis , Mutation , Orotic Acid/analogs & derivatives , Phenotype , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae/metabolism
6.
Proc Natl Acad Sci U S A ; 96(7): 3757-62, 1999 Mar 30.
Article in English | MEDLINE | ID: mdl-10097110

ABSTRACT

Yeast centromeric DNA (CEN DNA) binding factor 3 (CBF3) is a multisubunit protein complex that binds to the essential CDEIII element in CEN DNA. The four CBF3 proteins are required for accurate chromosome segregation and are considered to be core components of the yeast kinetochore. We have examined the structure of the CBF3-CEN DNA complex by atomic force microscopy. Assembly of CBF3-CEN DNA complexes was performed by combining purified CBF3 proteins with a DNA fragment that includes the CEN region from yeast chromosome III. Atomic force microscopy images showed DNA molecules with attached globular bodies. The contour length of the DNA containing the complex is approximately 9% shorter than the DNA alone, suggesting some winding of DNA within the complex. The measured location of the single binding site indicates that the complex is located asymmetrically to the right of CDEIII extending away from CDEI and CDEII, which is consistent with previous data. The CEN DNA is bent approximately 55 degrees at the site of complex formation. A significant fraction of the complexes are linked in pairs, showing three to four DNA arms, with molecular volumes approximately three times the mean volumes of two-armed complexes. These multi-armed complexes indicate that CBF3 can bind two DNA molecules together in vitro and, thus, may be involved in holding together chromatid pairs during mitosis.


Subject(s)
Centromere/ultrastructure , DNA, Fungal/metabolism , DNA, Fungal/ultrastructure , DNA-Binding Proteins/metabolism , DNA-Binding Proteins/ultrastructure , Fungal Proteins/metabolism , Fungal Proteins/ultrastructure , Nuclear Proteins , Saccharomyces cerevisiae Proteins , Saccharomyces cerevisiae/genetics , Saccharomyces cerevisiae/ultrastructure , Chromosome Mapping , Chromosomes, Fungal/ultrastructure , DNA, Fungal/chemistry , DNA-Binding Proteins/chemistry , Fungal Proteins/chemistry , Kinetochores , Microscopy, Atomic Force
7.
Mol Gen Genet ; 260(1): 20-9, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9829824

ABSTRACT

The Cbf5 protein of Saccharomyces cerevisiae was originally identified as a low-affinity centromeric DNA-binding protein, and chf5 mutants have a defect in rRNA synthesis. A closely related protein from mammals, NAP57, is a nucleolar protein that coimmunoprecipitates with the nucleolar phosphoprotein Nopp140. To study the function of this protein family in a higher eukaryote that is amenable to genetic approaches, the gene encoding a Drosophila melanogaster homolog, Nop60B, was identified. The predicted Drosophila protein shares a high degree of sequence identity over a 380-residue region with both the mammalian and yeast proteins, and shares several conserved motifs with the prokaryotic tRNA pseudouridine 55 synthases. Nop60B RNA is found at high levels in nurse cells and in the oocyte, and is present throughout development. Nop60B protein is localized primarily to the nucleolus of interphase cells, and is absent from the chromosomes during mitosis. Nop60B mutants were generated and shown to be homozygous lethal. The Drosophila gene can rescue the lethal phenotype of yeast chf5 mutations, showing that the function of this protein has been conserved from yeast to Drosophila.


Subject(s)
Cell Nucleolus/chemistry , Drosophila Proteins , Drosophila/genetics , Genes, Essential , Genes, Insect , Hydro-Lyases , Nuclear Proteins/genetics , Ribonucleoproteins, Small Nuclear , Saccharomyces cerevisiae Proteins , Amino Acid Sequence , Animals , Cell Compartmentation , Gene Expression , Genetic Complementation Test , Intramolecular Lyases/genetics , Intramolecular Transferases , Microtubule-Associated Proteins/genetics , Molecular Sequence Data , Multigene Family , RNA-Binding Proteins/genetics , Sequence Homology, Amino Acid , Tissue Distribution , Yeasts/genetics
8.
Mol Cell Biol ; 18(9): 5465-77, 1998 Sep.
Article in English | MEDLINE | ID: mdl-9710630

ABSTRACT

DNA from the centromere region of linkage group (LG) VII of Neurospora crassa was cloned previously from a yeast artificial chromosome library and was found to be atypical of Neurospora DNA in both composition (AT rich) and complexity (repetitive). We have determined the DNA sequence of a small portion (approximately 16.1 kb) of this region and have identified a cluster of three new retrotransposon-like elements as well as degenerate fragments from the 3' end of Tad, a previously identified LINE-like retrotransposon. This region contains a novel full-length but nonmobile copia-like element, designated Tcen, that is only associated with centromere regions. Adjacent DNA contains portions of a gypsy-like element designated Tgl1. A third new element, Tgl2, shows similarity to the Ty3 transposon of Saccharomyces cerevisiae. All three of these elements appear to be degenerate, containing predominantly transition mutations suggestive of the repeat-induced point mutation (RIP) process. Three new simple DNA repeats have also been identified in the LG VII centromere region. While Tcen elements map exclusively to centromere regions by restriction fragment length polymorphism analysis, the defective Tad elements appear to occur most frequently within centromeres but are also found at other loci including telomeres. The characteristics and arrangement of these elements are similar to those seen in the Drosophila centromere, but the relative abundance of each class of repeats, as well as the sequence degeneracy of the transposon-like elements, is unique to Neurospora. These results suggest that the Neurospora centromere is heterochromatic and regional in character, more similar to centromeres of Drosophila than to those of most single-cell yeasts.


Subject(s)
Centromere/genetics , Chromosomes, Fungal , DNA Transposable Elements , Neurospora crassa/genetics , Repetitive Sequences, Nucleic Acid , Algorithms , Amino Acid Sequence , Animals , Base Sequence , Blotting, Southern , Centromere/chemistry , Chromosome Mapping , DNA, Fungal/chemistry , DNA, Fungal/genetics , Drosophila/genetics , Endopeptidases/chemistry , Endopeptidases/genetics , Genetic Linkage , Molecular Sequence Data , Moloney murine leukemia virus/genetics , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Protein Biosynthesis , RNA-Directed DNA Polymerase/chemistry , RNA-Directed DNA Polymerase/genetics , Retroelements , Sequence Alignment , Sequence Homology, Amino Acid , Sequence Homology, Nucleic Acid , Telomere/chemistry , Telomere/genetics
9.
Mol Cell Biol ; 17(10): 6175-83, 1997 Oct.
Article in English | MEDLINE | ID: mdl-9315678

ABSTRACT

Yeast Cbf5p was originally isolated as a low-affinity centromeric DNA binding protein (W. Jiang, K. Middleton, H.-J. Yoon, C. Fouquet, and J. Carbon, Mol. Cell. Biol. 13:4884-4893, 1993). Cbf5p also binds microtubules in vitro and interacts genetically with two known centromere-related protein genes (NDC10/CBF2 and MCK1). However, Cbf5p was found to be nucleolar and is highly homologous to the rat nucleolar protein NAP57, which coimmunoprecipitates with Nopp140 and which is postulated to be involved in nucleolar-cytoplasmic shuttling (U. T. Meier, and G. Blobel, J. Cell Biol. 127:1505-1514, 1994). The temperature-sensitive cbf5-1 mutant demonstrates a pronounced defect in rRNA biosynthesis at restrictive temperatures, while tRNA transcription and pre-rRNA and pre-tRNA cleavage processing appear normal. The cbf5-1 mutant cells are deficient in cytoplasmic ribosomal subunits at both permissive and restrictive temperatures. A high-copy-number yeast genomic library was screened for genes that suppress the cbf5-1 temperature-sensitive growth phenotype. SYC1 (suppressor of yeast cbf5-1) was identified as a multicopy suppressor of cbf5-1 and subsequently was found to be identical to RRN3, an RNA polymerase I transcription factor. A cbf5delta null mutant is not rescued by plasmid pNOY103 containing a yeast 35S rRNA gene under the control of a Pol II promoter, indicating that Cbf5p has one or more essential functions in addition to its role in rRNA transcription.


Subject(s)
Fungal Proteins/physiology , Hydro-Lyases , Microtubule-Associated Proteins/physiology , Pol1 Transcription Initiation Complex Proteins , RNA, Fungal/biosynthesis , RNA, Ribosomal/biosynthesis , Ribonucleoproteins, Small Nuclear , Saccharomyces cerevisiae Proteins , Saccharomyces cerevisiae/genetics , Transcription Factors/physiology , Cytoplasm/chemistry , Fungal Proteins/genetics , Genes, Fungal/genetics , Genes, Suppressor/genetics , Microtubule-Associated Proteins/genetics , Mutation , RNA Polymerase I , RNA Processing, Post-Transcriptional , RNA, Ribosomal/metabolism , RNA, Transfer/biosynthesis , Restriction Mapping , Ribosomes/chemistry , Saccharomyces cerevisiae/enzymology , Temperature , Transcription Factors/genetics , Transcription, Genetic/physiology
10.
J Cell Biol ; 136(3): 487-500, 1997 Feb 10.
Article in English | MEDLINE | ID: mdl-9024682

ABSTRACT

Genetic and biochemical strategies have been used to identify Schizosaccharomyces pombe proteins with roles in centromere function. One protein, identified by both approaches, shows significant homology to the human centromere DNA-binding protein, CENP-B, and is identical to Abp1p (autonomously replicating sequence-binding protein 1) (Murakami, Y., J.A. Huberman, and J. Hurwitz. 1996. Proc. Natl. Acad. Sci. USA. 93:502-507). Abp1p binds in vitro specifically to at least three sites in centromeric central core DNA of S. pombe chromosome II (cc2). Overexpression of abp1 affects mitotic chromosome stability in S. pombe. Although inactivation of the abp1 gene is not lethal, the abp1 null strain displays marked mitotic chromosome instability and a pronounced meiotic defect. The identification of a CENP-B-related centromere DNA-binding protein in S. pombe strongly supports the hypothesis that fission yeast centromeres are structurally and functionally related to the centromeres of higher eukaryotes.


Subject(s)
Autoantigens , DNA-Binding Proteins/genetics , Fungal Proteins/genetics , Microfilament Proteins , Saccharomyces cerevisiae Proteins , Schizosaccharomyces/metabolism , Amino Acid Sequence , Base Sequence , Binding Sites , Centromere , Centromere Protein B , Chromosomal Proteins, Non-Histone/chemistry , Chromosomes , DNA, Fungal , DNA-Binding Proteins/chemistry , DNA-Binding Proteins/metabolism , Fungal Proteins/chemistry , Fungal Proteins/metabolism , Genes, Fungal , Humans , Meiosis , Mitosis , Molecular Sequence Data , Schizosaccharomyces/genetics , Sequence Homology, Amino Acid
11.
Mol Cell Biol ; 15(9): 4835-42, 1995 Sep.
Article in English | MEDLINE | ID: mdl-7651401

ABSTRACT

CBF2/NDC10/CTF14 encodes the 110-kDa subunit of CBF3, a key component of the yeast centromere/kinetochore. Overexpression of yeast CDC34 specifically suppresses the temperature-sensitive growth phenotype of the ndc10-1 mutation. Mutations in CDC34, which specifies a ubiquitin-conjugating enzyme, arrest yeast cells in the G1 phase of the cell cycle, with no intact spindles formed (M. G. Goebl, J. Yochem, S. Jentsch, J. P. McGrath, A. Varshavsky, and B. Byers, Science 241:1331-1335, 1988). The cdc34-2 mutation drastically alters the pattern of Cbf2p modification. Results of experiments using antibodies against Cbf2p and ubiquitin indicate that Cbf2p is ubiquitinated in vivo. Purified Cdc34p catalyzes the formation of Cbf2p-monoubiquitin conjugate in vitro. These data suggest that Cbf2p is an endogenous substrate of the CDC34 ubiquitin-conjugating enzyme and imply that ubiquitination of a kinetochore protein plays a regulatory role in kinetochore function.


Subject(s)
DNA-Binding Proteins/metabolism , Fungal Proteins/metabolism , Kinetochores/metabolism , Ligases/metabolism , Saccharomyces cerevisiae Proteins , Saccharomyces cerevisiae/genetics , Ubiquitin-Protein Ligase Complexes , Anaphase-Promoting Complex-Cyclosome , DNA-Binding Proteins/genetics , Fungal Proteins/genetics , Gene Dosage , Ligases/genetics , Mutation , Protein Processing, Post-Translational , Recombinant Proteins/metabolism , Saccharomyces cerevisiae/metabolism , Suppression, Genetic , Ubiquitin-Conjugating Enzymes , Ubiquitin-Protein Ligases , Ubiquitins/metabolism
12.
Mol Gen Genet ; 246(3): 360-6, 1995 Feb 06.
Article in English | MEDLINE | ID: mdl-7854321

ABSTRACT

We find that overexpression in yeast of the yeast MCK1 gene, which encodes a meiosis and centromere regulatory kinase, suppresses the temperature-sensitive phenotype of certain mutations in essential centromere binding protein genes CBF2 and CBF5. Since Mck1p is a known serine/threonine protein kinase, this suppression is postulated to be due to Mck1p-catalyzed in vivo phosphorylation of centromere binding proteins. Evidence in support of this model was provided by the finding that purified Mck1p phosphorylates in vitro the 110 kDa subunit (Cbf2p) of the multimeric centromere binding factor CBF3. This phosphorylation occurs on both serine and threonine residues in Cbf2p.


Subject(s)
Fungal Proteins/genetics , Hydro-Lyases , Microtubule-Associated Proteins/genetics , Protein-Tyrosine Kinases/biosynthesis , Ribonucleoproteins, Small Nuclear , Ribonucleoproteins , Saccharomyces cerevisiae Proteins , Suppression, Genetic/genetics , Fungal Proteins/metabolism , Gene Dosage , Gene Expression Regulation, Fungal , Genes, Fungal/genetics , Glycogen Synthase Kinase 3 , Phosphorylation , Protein-Tyrosine Kinases/genetics , Protein-Tyrosine Kinases/metabolism , Saccharomyces cerevisiae/enzymology , Saccharomyces cerevisiae/genetics , Serine/metabolism , Temperature , Threonine/metabolism
13.
Proc Natl Acad Sci U S A ; 91(15): 7212-6, 1994 Jul 19.
Article in English | MEDLINE | ID: mdl-8041770

ABSTRACT

We have used in vitro motility assays to investigate the mechanism of kinetochore function in the budding yeast Saccharomyces cerevisiae. Functional centromeric DNA plus a tripartite centromere binding protein complex, CBF3, was found to be necessary but not sufficient for in vitro kinetochore activity. A fourth required component was identified as the motor protein Kar3p, a previously reported yeast kinesin known to be involved in karyogamy and mitosis. Our data support genetic evidence suggesting that Kar3p is a kinetochore-associated motor and imply that CBF3 plays a regulatory role in kinetochore function.


Subject(s)
Centromere/physiology , DNA-Binding Proteins/physiology , Fungal Proteins/physiology , Kinesins/physiology , Microtubule-Associated Proteins , Nuclear Proteins , Saccharomyces cerevisiae Proteins , Saccharomyces cerevisiae/physiology , Chromosomes, Fungal , Kinetochores
14.
Mol Cell Biol ; 14(2): 1510-9, 1994 Feb.
Article in English | MEDLINE | ID: mdl-7904723

ABSTRACT

The centromere locus from linkage group VII of Neurospora crassa has been cloned, characterized, and physically mapped. The centromeric DNA is contained within a 450-kb region that is recombination deficient, A+T-rich, and contains repetitive sequences. Repetitive sequences from within this region hybridize to a family of repeats located at or near centromeres in all seven linkage groups of N. crassa. Genomic Southern blots and sequence analysis of these repeats revealed a unique centromere structure containing a divergent family of centromere-specific repeats. The predominantly transitional differences between copies of the centromere-specific sequence repeats and their high A+T content suggest that their divergence was mediated by repeat-induced point (RIP) mutations.


Subject(s)
Centromere/physiology , DNA, Fungal/genetics , Neurospora crassa/genetics , Base Composition , Base Sequence , Blotting, Southern , Centromere/chemistry , Chromosome Walking , Chromosomes, Artificial, Yeast , Chromosomes, Fungal , Cloning, Molecular/methods , DNA, Fungal/chemistry , Deoxyribonucleases, Type II Site-Specific , Escherichia coli , Genetic Linkage , Molecular Sequence Data , Polymorphism, Restriction Fragment Length , Repetitive Sequences, Nucleic Acid , Restriction Mapping , Sequence Homology, Nucleic Acid
15.
Mol Cell Biol ; 13(8): 4884-93, 1993 Aug.
Article in English | MEDLINE | ID: mdl-8336724

ABSTRACT

Yeast centromere DNA (CEN) affinity column chromatography has been used to purify several putative centromere and kinetochore proteins from yeast chromatin extracts. The single yeast gene (CBF5) specifying one of the major low-affinity centromere-binding proteins (p64'/CBF5p) has been cloned and shown to be essential for viability of Saccharomyces cerevisiae. CBF5 specifies a 55-kDa highly charged protein that contains a repeating KKD/E sequence domain near the C terminus, similar to known microtubule-binding domains in microtubule-associated proteins 1A and 1B, CBF5p, obtained by overexpression in bacterial cells, binds microtubules in vitro, whereas C-terminal deleted proteins lacking the (KKD/E)n domain do not. Dividing yeast cells containing a C-terminal truncated CBF5 gene, producing CBF5p containing only three copies of the KKD/E repeat, delay with replicated genomes at the G2/M phase of the cell cycle, while depletion of CBF5p arrests most cells in G1/S. Overproduction of CBF5p in S. cerevisiae complements a temperature sensitivity mutation in the gene (CBF2) specifying the 110-kDa subunit of the high-affinity CEN DNA-binding factor CBF3, suggesting in vivo interaction of CBF5p and CBF3. A second low-affinity centromere-binding factor has been identified as topoisomerase II.


Subject(s)
Centromere/metabolism , DNA-Binding Proteins/metabolism , Fungal Proteins/metabolism , Genes, Fungal , Hydro-Lyases , Microtubule-Associated Proteins/metabolism , Microtubules/metabolism , Ribonucleoproteins, Small Nuclear , Saccharomyces cerevisiae Proteins , Base Sequence , Cell Cycle , Cell Division , Chromosome Mapping , Cloning, Molecular , Fungal Proteins/genetics , Macromolecular Substances , Microtubule-Associated Proteins/genetics , Molecular Sequence Data , Oligonucleotides/chemistry , Sequence Homology, Amino Acid , Structure-Activity Relationship
16.
J Cell Biol ; 121(3): 513-9, 1993 May.
Article in English | MEDLINE | ID: mdl-8486733

ABSTRACT

We have cloned and determined the nucleotide sequence of the gene (CBF2) specifying the large (110 kD) subunit of the 240-kD multisubunit yeast centromere binding factor CBF3, which binds selectively in vitro to yeast centromere DNA and contains a minus end-directed microtubule motor activity. The deduced amino acid sequence of CBF2p shows no sequence homologies with known molecular motors, although a consensus nucleotide binding site is present. The CBF2 gene is essential for viability of yeast and is identical to NDC10, in which a conditional mutation leads to a defect in chromosome segregation (Goh, P.-Y., and J. V. Kilmartin, in this issue of The Journal of Cell Biology). The combined in vitro and in vivo evidence indicate that CBF2p is a key component of the budding yeast kinetochore.


Subject(s)
Centromere/metabolism , DNA-Binding Proteins/genetics , Fungal Proteins/genetics , Genes, Fungal , Saccharomyces cerevisiae Proteins , Saccharomyces cerevisiae/genetics , Amino Acid Sequence , Base Sequence , Consensus Sequence , GTP-Binding Proteins/genetics , Kinetochores , Microtubules/metabolism , Molecular Sequence Data , Molecular Weight
18.
Nature ; 359(6395): 533-6, 1992 Oct 08.
Article in English | MEDLINE | ID: mdl-1406970

ABSTRACT

During cell division, sister chromosomes segregate from each other on a microtubule-based structure called the mitotic spindle. Proteins bind to the centromere, a region of chromosomal DNA, to form the kinetochore, which mediates chromosome attachment to the mitotic spindle microtubules. In the budding yeast Saccharomyces cerevisiae, genetic analysis has shown that the 28-basepair (bp) CDEIII region of the 125-bp centromere DNA sequence (CEN sequence) is the main region controlling chromosome segregation in vivo. Therefore it is likely that proteins binding to the CDEIII region link the centromeres to the microtubules during mitosis. A complex of proteins (CBF3) that binds specifically to the CDEIII DNA sequence has been isolated by affinity chromatography. Here we describe kinetochore function in vitro. The CBF3 complex can link DNA to microtubules, and the complex contains a minus-end-directed microtubule-based motor. We suggest that microtubule-based motors form the fundamental link between microtubules and chromosomes at mitosis.


Subject(s)
DNA-Binding Proteins/metabolism , Fungal Proteins/metabolism , Microtubules/physiology , Saccharomyces cerevisiae/ultrastructure , Adenosine Triphosphate/metabolism , Binding, Competitive , Centromere/metabolism , Chromosomes, Fungal/physiology , DNA, Fungal/metabolism , DNA-Binding Proteins/isolation & purification , Fungal Proteins/isolation & purification , Movement
19.
Genetics ; 132(1): 39-51, 1992 Sep.
Article in English | MEDLINE | ID: mdl-1398062

ABSTRACT

We have designed a colony color assay for monitoring centromere DNA-protein interactions in yeast (Saccharomyces cerevisiae). The assay is based on the ability of centromere DNA sequences to block (in cis) transcription initiated from a hybrid CEN-GAL1 promoter. Using a IacZ reporter gene under control of the CEN-GAL1 promoter, we screened colonies derived from mutagenized cells for a blue color phenotype indicative of derepression of the hybrid construct. A limited screen in which a 61-bp CEN11 DNA fragment containing an intact CDEIII subregion plus flanking sequences was used as the "pseudo-operator" led to the identification of mutations (blu) in three complementation groups. The blu1 mutants exhibited a decrease in activity of the major CEN DNA-binding proteins in vitro. The BLU1 gene was shown to be identical to the previously isolated SPT3 gene, known to be involved in the transcriptional regulation of a subset of yeast genes. Our results indicate that the BLU1/SPT3 gene product may also be required to maintain optimal levels of functional centromere DNA-binding proteins.


Subject(s)
Centromere , DNA, Fungal/metabolism , DNA-Binding Proteins/genetics , Fungal Proteins/genetics , Mutation , Saccharomyces cerevisiae Proteins , Saccharomyces cerevisiae/genetics , Acriflavine , Base Sequence , Colorimetry , DNA-Binding Proteins/metabolism , Flow Cytometry , Fungal Proteins/metabolism , Genes, Dominant , Genes, Fungal , Genes, Recessive , Genetic Complementation Test , Molecular Sequence Data , Plasmids , Saccharomyces cerevisiae/ultrastructure , Transcription Factors , beta-Galactosidase/genetics
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