RESUMO
Through a screen designed to isolate novel fission yeast genes required for chromosome segregation, we have identified mal3+. The mal3-1 mutation decreased the transmission fidelity of a nonessential minichromosome and altered sensitivity to microtubule-destabilizing drugs. Sequence analysis revealed that the 35-kD Mal3 is a member of an evolutionary conserved protein family. Its human counterpart EB-1 was identified in an interaction screen with the tumour suppressor protein APC. EB-1 was able to substitute for the complete loss of the mal3+ gene product suggesting that the two proteins might have similar functions. Cells containing a mal3 null allele were viable but showed a variety of phenotypes, including impaired control of cell shape. A fusion protein of Mal3 with the Aequorea victoria green fluorescent protein led to in vivo visualization of both cytoplasmic and mitotic microtubule structures indicating association of Mal3 with microtubules. The absence of Mal3 protein led to abnormally short, often faint cytoplasmic microtubules as seen by indirect antitubulin immunofluorescence. While loss of the mal3+ gene product had no gross effect on mitotic spindle morphology, overexpression of mal3+ compromised spindle formation and function and led to severe growth inhibition and abnormal cell morphology. We propose that Mal3 plays a role in regulating the integrity of microtubules possibly by influencing their stability.
Assuntos
Proteínas do Citoesqueleto , Proteínas Fúngicas/fisiologia , Proteínas Associadas aos Microtúbulos/fisiologia , Microtúbulos/fisiologia , Proteínas de Schizosaccharomyces pombe , Schizosaccharomyces/fisiologia , Polipose Adenomatosa do Colo , Proteína da Polipose Adenomatosa do Colo , Sequência de Aminoácidos , Divisão Celular/genética , Divisão Celular/fisiologia , Tamanho Celular/genética , Tamanho Celular/fisiologia , Clonagem Molecular , Contagem de Colônia Microbiana , Sequência Conservada , Proteínas do Citoesqueleto/genética , Proteínas do Citoesqueleto/fisiologia , Evolução Molecular , Proteínas Fúngicas/biossíntese , Proteínas Fúngicas/genética , Deleção de Genes , Regulação Fúngica da Expressão Gênica , Humanos , Interfase/genética , Proteínas Associadas aos Microtúbulos/biossíntese , Proteínas Associadas aos Microtúbulos/genética , Microtúbulos/genética , Dados de Sequência Molecular , Família Multigênica , Mutação , Fenótipo , Schizosaccharomyces/genética , Schizosaccharomyces/crescimento & desenvolvimento , Homologia de Sequência de Aminoácidos , Fuso Acromático/genética , Fuso Acromático/fisiologiaRESUMO
The functions of many open reading frames (ORFs) identified in genome-sequencing projects are unknown. New, whole-genome approaches are required to systematically determine their function. A total of 6925 Saccharomyces cerevisiae strains were constructed, by a high-throughput strategy, each with a precise deletion of one of 2026 ORFs (more than one-third of the ORFs in the genome). Of the deleted ORFs, 17 percent were essential for viability in rich medium. The phenotypes of more than 500 deletion strains were assayed in parallel. Of the deletion strains, 40 percent showed quantitative growth defects in either rich or minimal medium.
Assuntos
Deleção de Genes , Genes Essenciais , Genoma Fúngico , Fases de Leitura Aberta , Saccharomyces cerevisiae/genética , Meios de Cultura , Regulação Fúngica da Expressão Gênica , Marcação de Genes , Genes Fúngicos , Fenótipo , Reação em Cadeia da Polimerase , Recombinação Genética , Saccharomyces cerevisiae/crescimento & desenvolvimentoRESUMO
The centromere DNA element I (CDEI) is an important component of Saccharomyces cerevisiae centromere DNA and carries the palindromic sequence CACRTG (R = purine) as a characteristic feature. In vivo, CDEI is bound by the helix-loop-helix protein CPF1. This article describes the in vivo analysis of all single-base-pair substitutions in CDEI in the centromere of an artificial chromosome and demonstrates the importance of the palindromic sequence for faithful chromosome segregation, supporting the notion that CPF1 binds as a dimer to this binding site. Mutational analysis of two conserved base pairs on the left and two nonconserved base pairs on the right of the CDEI palindrome revealed that these are also relevant for mitotic CEN function. Symmetrical mutations in either half-site of the palindrome affect centromere activity to a different extent, indicating nonidentical sequence requirements for binding by the CPF1 homodimer. Analysis of double point mutations in CDEI and in CDEIII, an additional centromere element, indicate synergistic effects between the DNA-protein complexes at these sites.
Assuntos
Centrômero/fisiologia , DNA Fúngico/genética , Proteínas de Ligação a DNA/metabolismo , Proteínas Fúngicas/metabolismo , Genes Fúngicos , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/genética , Sequência de Bases , Fatores de Transcrição de Zíper de Leucina e Hélice-Alça-Hélix Básicos , Sítios de Ligação , Centrômero/efeitos dos fármacos , Cicloeximida/farmacologia , DNA Fúngico/metabolismo , Escherichia coli/genética , Dados de Sequência Molecular , Mutagênese Sítio-Dirigida , Sondas de Oligonucleotídeos , PlasmídeosRESUMO
In the yeast Saccharomyces cerevisiae, the complete information needed in cis to specify a fully functional mitotic and meiotic centromere is contained within 120 bp arranged in the three conserved centromeric (CEN) DNA elements CDEI, -II, and -III. The 25-bp CDEIII is most important for faithful chromosome segregation. We have constructed single- and double-base substitutions in all highly conserved residues and one nonconserved residue of this element and analyzed the mitotic in vivo function of the mutated CEN DNAs, using an artificial chromosome. The effects of the mutations on chromosome segregation vary between wild-type-like activity (chromosome loss rate of 4.8 x 10(-4)) and a complete loss of CEN function. Data obtained by saturation mutagenesis of the palindromic core sequence suggest asymmetric involvement of the palindromic half-sites in mitotic CEN function. The poor CEN activity of certain single mutations could be improved by introducing an additional single mutation. These second-site suppressors can be found at conserved and nonconserved positions in CDEIII. Our suppression data are discussed in the context of natural CDEIII sequence variations found in the CEN sequences of different yeast chromosomes.
Assuntos
Centrômero/fisiologia , Cromossomos Fúngicos/fisiologia , DNA Fúngico/genética , Mitose/genética , Saccharomyces cerevisiae/genética , Sequência de Bases , Deleção Cromossômica , Variação Genética/genética , Dados de Sequência Molecular , Mutagênese/genética , Oligonucleotídeos/genética , Sequências Repetitivas de Ácido Nucleico/fisiologia , Saccharomyces cerevisiae/fisiologiaRESUMO
By a screen designed to isolate new fission yeast genes required for chromosome segregation, we have identified mal2+. The conditionally lethal mal2-1 allele gives rise to increased loss of a nonessential minichromosome at the permissive temperature and leads to severe missegregation of the chromosomes at the nonpermissive temperature. Cloning by complementation and subsequent sequence analysis revealed that mal2 is a novel protein with a mass of 34 kDa. Cells containing a mal2 null allele were inviable, indicating that mal2+ is an essential gene. Fusion of mal2 protein to the green fluorescent protein (GFP) showed that mal2 was predominantly localized in the nucleus. Sensitivity to microtubule-destabilizing drugs and strong genetic interactions with alpha1-tubulin suggest an interaction of the mal2 protein with the microtubule system. Spindle formation and elongation were not detectably affected in the mal2-1 mutant as determined by indirect immunofluorescence. However, anomalous chromosome movement on the spindle leading to aberrant distribution of the chromosomal material was observed.
Assuntos
Cromossomos Fúngicos , Genes Fúngicos , Proteínas Nucleares/genética , Proteínas de Schizosaccharomyces pombe , Schizosaccharomyces/genética , Alelos , Sequência de Aminoácidos , Sequência de Bases , Primers do DNA , Metanossulfonato de Etila , Genes Letais , Proteínas de Fluorescência Verde , Proteínas Luminescentes/biossíntese , Dados de Sequência Molecular , Mutagênese , Proteínas Nucleares/biossíntese , Fenótipo , Reação em Cadeia da Polimerase , Proteínas Recombinantes de Fusão/biossíntese , Schizosaccharomyces/citologia , Schizosaccharomyces/crescimento & desenvolvimentoRESUMO
Saccharomyces cerevisiae centromeres have a characteristic 120-base-pair region consisting of three distinct centromere DNA sequence elements (CDEI, CDEII, and CDEIII). We have generated a series of 26 CEN mutations in vitro (including 22 point mutations, 3 insertions, and 1 deletion) and tested their effects on mitotic chromosome segregation by using a new vector system. The yeast transformation vector pYCF5 was constructed to introduce wild-type and mutant CEN DNAs onto large, linear chromosome fragments which are mitotically stable and nonessential. Six point mutations in CDEI show increased rates of chromosome loss events per cell division of 2- to 10-fold. Twenty mutations in CDEIII exhibit chromosome loss rates that vary from wild type (10(-4)) to nonfunctional (greater than 10(-1)). These results directly identify nucleotides within CDEI and CDEIII that are required for the specification of a functional centromere and show that the degree of conservation of an individual base does not necessarily reflect its importance in mitotic CEN function.
Assuntos
Centrômero/análise , Cromossomos/análise , DNA/análise , Mutação , Saccharomyces cerevisiae/genética , Sequência de Bases , Eletroforese em Gel de Ágar , Mitose , PlasmídeosRESUMO
Saccharomyces cerevisiae centromeres contain a conserved region ranging from 111 to 119 base pairs (bp) in length, which is characterized by the three conserved DNA elements CDEI, CDEII, and CDEIII. We isolated a 125-bp CEN6 DNA fragment (named ML CEN6) containing only these conserved elements and assayed it completely separated from its chromosomal context on circular minichromosomes and on a large linear chromosome fragment. The results show that this 125-bp CEN6 DNA fragment is by itself sufficient for complete mitotic and meiotic centromere functions.
Assuntos
Centrômero/fisiologia , Cromossomos/fisiologia , DNA Fúngico/fisiologia , Mitose , Saccharomyces cerevisiae/genética , Sequência de Bases , Clonagem Molecular , Enzimas de Restrição do DNA , Meiose , Dados de Sequência Molecular , Não Disjunção Genética , Plasmídeos , Saccharomyces cerevisiae/citologiaRESUMO
Heterologous markers are important tools required for the molecular dissection of gene function in many organisms, including Saccharomyces cerevisiae. Moreover, the presence of gene families and isoenzymes often makes it necessary to delete more than one gene. We recently introduced a new and efficient gene disruption cassette for repeated use in budding yeast, which combines the heterologous dominant kan(r) resistance marker with a Cre/loxP-mediated marker removal procedure. Here we describe an additional set of four completely heterologous loxP-flanked marker cassettes carrying the genes URA3 and LEU2 from Kluyveromyces lactis, his5(+) from Schizosaccharomyces pombe and the dominant resistance marker ble(r) from the bacterial transposon Tn5, which confers resistance to the antibiotic phleomycin. All five loxP--marker gene--loxP gene disruption cassettes can be generated using the same pair of oligonucleotides and all can be used for gene disruption with high efficiency. For marker rescue we have created three additional Cre expression vectors carrying HIS3, TRP1 or ble(r) as the yeast selection marker. The set of disruption cassettes and Cre expression plasmids described here represents a significant further development of the marker rescue system, which is ideally suited to functional analysis of the yeast genome.
Assuntos
Aldose-Cetose Isomerases , Proteínas de Bactérias , Deleção de Genes , Integrases/metabolismo , Mutagênese Insercional/métodos , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/genética , Proteínas Virais/metabolismo , 3-Isopropilmalato Desidrogenase , Acetiltransferases/genética , Oxirredutases do Álcool/genética , Sequência de Bases , Proteínas Fúngicas/genética , Marcadores Genéticos , Hidroliases/genética , Resistência a Canamicina , Modelos Genéticos , Dados de Sequência Molecular , Oligonucleotídeos/genética , Organismos Geneticamente Modificados , Plasmídeos , Transformação GenéticaRESUMO
The G1-specific D- and E-type cyclins are among the most crucial factors controlling cell cycle progression in mammalian cells and are therefore thought to play an important role in tumorigenisis. D-type cyclins have indeed been shown to be endowed with an oncogenic potential. Here, we report that the ectopic expression of human cyclin E, but not cyclin D1, deregulates DNA synthesis in both yeast and mammalian cells. In yeast, induction of DNA synthesis by cyclin E occurs even under conditions of cell cycle arrest in G1 or G2/M, indicating an uncoupling of DNA replication from cell cycle progression. In rat embryo fibroblasts, the cooperative action of Ras and cyclin E induces transformation. These cells, in contrast to those transformed by Ras and cyclin D1, show aberrant levels of DNA synthesis. Since cyclin E is commonly overexpressed in a variety of human tumors, these findings may point to a link between the uncontrolled proliferation and the genomic instability typically seen in malignant tumors. Furthermore they reveal significant differences in the functional properties of cyclin E and D1.
Assuntos
Ciclinas/metabolismo , DNA/biossíntese , Fase G1/fisiologia , Fase G2/fisiologia , Animais , Linhagem Celular , Linhagem Celular Transformada , Ciclina D , Replicação do DNA , Fibroblastos/metabolismo , Fibroblastos/fisiologia , Fase G1/genética , Fase G2/genética , Humanos , Ratos , Saccharomyces cerevisiae/genéticaRESUMO
We have employed a system that utilizes homologous pairs of human DNA-derived yeast artificial chromosomes (YACs) as marker chromosomes to assess the specific role(s) of conserved centromere DNA elements (CDEI, CDEII and CDEIII) in meiotic chromosome disjunction fidelity. Thirteen different centromere (CEN) mutations were tested for their effects on meiotic centromere function. YACs containing a wild-type CEN DNA sequence segregate with high fidelity in meiosis I (99% normal segregation) and in meiosis II (96% normal segregation). YACs containing a 31-bp deletion mutation in centromere DNA element II (CDEII delta 31) in either a heterocentric (mutant/wild type), homocentric (mutant/mutant) or monosomic (mutant/--) YAC pair configuration exhibited high levels (16-28%) of precocious sister-chromatid segregation (PSS) and increased levels (1-6%) of nondisjunction meiosis I (NDI). YACs containing this mutation also exhibit high levels (21%) of meiosis II nondisjunction. Interestingly, significant alterations in homolog recombination frequency were observed in the exceptional PSS class of tetrads, suggesting unusual interactions between prematurely separated sister chromatids and their homologous nonsister chromatids. We also have assessed the meiotic segregation effects of rare gene conversion events occurring at sites located immediately adjacent to or distantly from the centromere region. Proximal gene conversion events were associated with extremely high levels (60%) of meiosis I segregation errors (including both PSS and NDI), whereas distal events had no apparent effect. Taken together, our results indicate a critical role for CDEII in meiosis and underscore the importance of maintaining sister-chromatid cohesion for proper recombination in meiotic prophase and for proper disjunction in meiosis I.
Assuntos
Centrômero/genética , Cromátides/fisiologia , Meiose/genética , Recombinação Genética/genética , Saccharomyces cerevisiae/genética , Sequência de Bases , Centrômero/metabolismo , Cromossomos Artificiais de Levedura/genética , Conversão Gênica , Deleção de Genes , Marcadores Genéticos , Humanos , Dados de Sequência Molecular , Ploidias , Mutação Puntual/genéticaRESUMO
The role of Chlamydia pneumoniae in the etiology of acute lower respiratory tract infections in infants and children is little understood. We studied the prevalence of C. pneumoniae infection in hospitalized infants and children with acute lower respiratory tract disease by cell culture, polymerase chain reaction (PCR), enzyme immunoassay and serology. Of 290 patients with a mean age of 3.7 years, only 3 (1%) were identified to be infected with C. pneumoniae. One child was positive in the cell culture as well as the PCR assay. Another infant was PCR-positive only and serologic evidence of infection was observed in a culture- and PCR-negative child. Chlamydia trachomatis was not detected in any patient specimen by either culture or PCR. Results of this study indicate that C. pneumoniae plays a minor role in the etiology of respiratory tract infections in infants and young children.
Assuntos
Infecções por Chlamydia/epidemiologia , Chlamydophila pneumoniae , Infecções Respiratórias/microbiologia , Doença Aguda , Adolescente , Distribuição por Idade , Criança , Pré-Escolar , Infecções por Chlamydia/diagnóstico , Infecções por Chlamydia/etiologia , Chlamydophila pneumoniae/isolamento & purificação , Feminino , Alemanha , Hospitalização , Humanos , Técnicas Imunoenzimáticas , Lactente , Recém-Nascido , Masculino , Reação em Cadeia da Polimerase , Prevalência , Infecções Respiratórias/diagnóstico , Infecções Respiratórias/epidemiologia , Testes SorológicosRESUMO
Stable maintenance of genetic information during meiosis and mitosis is dependent on accurate chromosome transmission. The centromere is a key component of the segregational machinery that couples chromosomes with the spindle apparatus. Most of what is known about the structure and function of the centromeres has been derived from studies on yeast cells. In Saccharomyces cerevisiae, the centromere DNA requirements for mitotic centromere function have been defined and some of the proteins required for an active complex have been identified. Centromere DNA and the centromere proteins form a complex that has been studied extensively at the chromatin level. Finally, recent findings suggest that assembly and activation of the centromere are integrated in the cell cycle.
Assuntos
Centrômero , Cromossomos Fúngicos/ultraestrutura , Kluyveromyces/citologia , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/citologia , Sequência de Bases , Fatores de Transcrição de Zíper de Leucina e Hélice-Alça-Hélix Básicos , Ciclo Celular , Sequência Consenso , DNA Fúngico/genética , Proteínas de Ligação a DNA/metabolismo , Proteínas Fúngicas/metabolismo , Cinetocoros , Kluyveromyces/genética , Kluyveromyces/fisiologia , Meiose , Mitose , Dados de Sequência Molecular , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/fisiologia , Homologia de Sequência do Ácido NucleicoRESUMO
We have analysed the centromeric chromatin from chromosome XIV of Saccharomyces cerevisiae at different stages of mitosis with the help of mutants of the cell division cycle. The pattern of centromeric chromatin in cells arrested using cdc20-1, tub2-401 and cdc15-1 alleles was indistinguishable from that of vegetatively growing cells, indicating that the centromeric complex is constitutively present during mitosis and possibly throughout the entire cell cycle. In contrast chromatin isolated from G0 cells and spores exhibited distinct differences in centromeric chromatin probably due to structural rearrangements of the centromeric complex. In particular the alterations found in spores are indicative of an inactive centromeric complex. The differences in centromeric chromatin in spores do not reflect a general reorganisation of the chromatin in this cell type, as the chromatin structure of the PHO3/PHO5 locus in spores was found to be identical to that in vegetative cells under repressed conditions. Thus the structural analysis of the centromere in different cell types provides evidence about the requirement of CEN DNA/protein complexes in different cell types and in different stages of the cell cycle.
Assuntos
Centrômero/química , Cromatina/química , Cromossomos Fúngicos/química , Proteínas de Transporte de Fosfato , Proteínas de Saccharomyces cerevisiae , Saccharomyces cerevisiae/química , Fosfatase Ácida , Proteínas de Transporte/genética , Ciclo Celular/genética , DNA Fúngico/genética , Proteínas Fúngicas/genética , Proteínas de Membrana Transportadoras/genética , Microtúbulos/metabolismo , Mitose , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/crescimento & desenvolvimento , Esporos FúngicosRESUMO
Isolated nuclei of Saccharomyces cerevisiae were incubated with five restriction nucleases. Out of the twenty-one recognition sequences for these nucleases in the centromere region of chromosome XIV, only five are accessible to cleavage. These sites map 11 bp and 74 bp to the left and 27 bp, 41 bp and 290 bp to the right, respectively, of the boundaries of the 118 bp functional CEN14 DNA sequence. The distance between the sites accessible to cleavage and closest to CEN14 is 156 bp, suggesting this is the maximal size of DNA protected in CEN14 chromatin. The DNA in CEN14 chromatin protected against cleavage with DNase I and micrococcal nuclease overlaps almost completely with this region. Hypersensitive regions flanking both sides are approximately 60 bp long. Analyses of other S. cerevisiae centromeres with footprinting techniques in intact cells or nucleolytic cleavages in isolated nuclei are discussed in relation to our results. We conclude that structural data of chromatin obtained with restriction nucleases are reliable and that the structure of CEN14 chromatin is representative for S. cerevisiae centromeres.
Assuntos
Centrômero/análise , Cromatina/análise , Cromossomos Fúngicos/análise , Cromossomos/análise , DNA Fúngico/análise , Saccharomyces cerevisiae/genética , Southern Blotting , Cromatina/metabolismo , DNA Fúngico/genética , Desoxirribonuclease I/metabolismo , Nuclease do Micrococo/metabolismo , Mapeamento por RestriçãoRESUMO
We have developed a system that utilizes human DNA-derived yeast artificial chromosomes (YACs) as marker chromosomes to study factors that contribute to the fidelity of meiotic chromosome transmission. Since aneuploidy for the YACs does not affect spore viability, different classes of meiotic missegregation can be scored accurately in four-viable-spore tetrads including precocious sister separation, meiosis I nondisjunction, meiotic chromatid loss, and meiosis II nondisjunction. Segregation of the homologous pair of 360-kilobase marker YACs was shown to occur with high fidelity in the first meiotic division and was associated with a high frequency of recombination within the human DNA segment. By using this experimental system, a series of YAC deletion derivatives ranging in size from 50 to 225 kilobases was analyzed to directly assess the relationship between meiotic recombination and meiosis I disjunction in a genotypically wild-type background. The relationship between physical distance and recombination frequency within the human DNA segment was measured to be comparable to that of endogenous yeast chromosomal DNA--ranging from less than 2.0 to 7.7 kilobases/centimorgan. Physical analysis of recombinant chromosomes detected no unequal crossing-over at dispersed repetitive elements distributed along the YACs. Recombination between YACs containing unrelated DNA segments was not observed. Furthermore, the segregational data indicated that meioses in which YAC pairs failed to recombine exhibited dramatically increased levels of meiosis I missegregation, including both precocious sister chromatid separation and nondisjunction.
Assuntos
Cromossomos Fúngicos/fisiologia , Cromossomos Humanos/fisiologia , Recombinação Genética , Saccharomyces cerevisiae/genética , Animais , DNA/genética , DNA/isolamento & purificação , Humanos , Meiose , Camundongos , Modelos GenéticosRESUMO
Chlamydia pneumoniae is an important human intracellular pathogen; however, the pathogenesis of C. pneumoniae infection is poorly understood, and the bacterial adherence mechanism to host cells is unknown. This study examined the role of glycosaminoglycans (GAGs) in the adhesion of C. pneumoniae to eukaryotic cells. Heparin and heparan sulfate were found to inhibit the attachment of C. pneumoniae to human epithelial cells. Reduction in infectivity resulted from the binding of heparin to the organism. Enzymatic removal of heparan sulfate moieties from the host cell surface led to a marked decrease in C. pneumoniae infectivity. Mutant CHO cell lines that were defective in heparan sulfate biosynthesis were less susceptible to C. pneumoniae infection than was the wild-type cell line. However, preincubation of the GAG-deficient CHO cells with exogenous heparin greatly increased infectivity.
Assuntos
Chlamydophila pneumoniae/patogenicidade , Células Epiteliais/efeitos dos fármacos , Heparina/metabolismo , Heparitina Sulfato/biossíntese , Receptores de Superfície Celular/metabolismo , Animais , Células CHO/efeitos dos fármacos , Adesão Celular/efeitos dos fármacos , Linhagem Celular/efeitos dos fármacos , Chlamydophila pneumoniae/isolamento & purificação , Chlamydophila pneumoniae/metabolismo , Cricetinae , Suscetibilidade a Doenças/metabolismo , Citometria de Fluxo , Fluorescência , Heparitina Sulfato/deficiência , HumanosRESUMO
Centromeres are essential components of eucaryotic chromosomes. In budding yeast, up to now, 15 of the 16 centromere DNAs have been isolated. Here we report the functional isolation and characterization of CEN8, the last of the yeast centromeres missing. The centromere consensus sequence for the 16 chromosomes in this organism is presented.
Assuntos
Centrômero/genética , Cromossomos Fúngicos , Saccharomyces cerevisiae/genética , Sequência de Bases , Clonagem Molecular , Sequência Consenso/genética , DNA Fúngico , Dados de Sequência Molecular , Análise de Sequência de DNARESUMO
Centromeres most likely consist of DNA (CEN DNA) interacting with specific proteins. In Saccharomyces cerevisiae a clear picture has emerged of a 120 bp sequence that is characteristic of CEN DNA. We have investigated the 25 bp centromere DNA element (CDEIII) that represents the right part of a CEN DNA. We showed using a series of mutants generated in vitro that the right most triple A of the consensus sequence TGT.T.TG.. TTCCGAA.....AAA participates in the assembly of a functional centromere and that no further sequences to the right are needed. Distance changes between the centre dyad TTCCGAA and the triple A have two effects: Addition of one base pair leads to a reduction, and addition of two or four base pairs to a loss of centromere function implying a participation of the centre dyad and the triple A region in protein binding. Indeed, a synthetic oligonucleotide of 39 bp containing CDEIII shows specific protein binding.
Assuntos
Centrômero/fisiologia , Cromossomos/fisiologia , Mutação , Saccharomyces cerevisiae/genética , Sequência de Bases , Enzimas de Restrição do DNA , Escherichia coli/genética , Plasmídeos , Saccharomyces cerevisiae/ultraestruturaRESUMO
A direct selection procedure has been used to isolate 11 distinct yeast genomic DNA fragments that eliminate the extreme segregation bias characteristic of autonomously replicating yeast plasmids. The selection scheme takes advantage of the fact that the cloned ochre suppressing tRNA gene, SUP11, is lethal at high copy number and therefore causes cell death when present on an ARS plasmid that lacks a cis-acting partition function. Each of the cloned DNA sequences was mapped to specific yeast chromosomes by hybridization to chromosome-sized DNA molecules separated by alternating field electrophoresis. Ten of the cloned fragments correspond to chromosomal centromeres; one fragment corresponds to the cis-acting locus required for endogenous 2 mu plasmid stability. Nucleotide sequence comparison of the ten centromere DNAs gives a new picture of conserved centromere DNA elements.
Assuntos
Centrômero/ultraestrutura , Cromossomos/ultraestrutura , Clonagem Molecular , DNA Fúngico/isolamento & purificação , Genes Fúngicos , Saccharomyces cerevisiae/ultraestrutura , Sequência de Bases , Enzimas de Restrição do DNA , Vetores Genéticos , PlasmídeosRESUMO
The centromere complex is a multicomponent structure essential for faithful chromosome transmission. Here we show that the S. cerevisiae centromere protein Cpf1 bends centromere DNA element I (CDEI) with the bend angle ranging from 66 degrees to 71 degrees. CDEI DNA sequences that carry point mutations which lead to reduced Cpf1 binding affinity and in vivo centromere activity are still able to show bending. The Cpf1 induced bend is directed towards the major groove with the bend centre located in CDEI. An intrinsic bend cannot replace the Cpf1 induced DNA bend for in vivo centromere function. An in vivo phasing experiment suggests that both the distance and the correct spatial arrangement of the CDEI/Cpf1 complex to CDEII and CDEIII are important for optimal centromere function.