ABSTRACT
The yeast Sir2 protein, required for transcriptional silencing, has an NAD(+)-dependent histone deacetylase (HDA) activity. Yeast extracts contain a NAD(+)-dependent HDA activity that is eliminated in a yeast strain from which SIR2 and its four homologs have been deleted. This HDA activity is also displayed by purified yeast Sir2p and homologous Archaeal, eubacterial, and human proteins, and depends completely on NAD(+) in all species tested. The yeast NPT1 gene, encoding an important NAD(+) synthesis enzyme, is required for rDNA and telomeric silencing and contributes to silencing of the HM loci. Null mutants in this gene have significantly reduced intracellular NAD(+) concentrations and have phenotypes similar to sir2 null mutants. Surprisingly, yeast from which all five SIR2 homologs have been deleted have relatively normal bulk histone acetylation levels. The evolutionary conservation of this regulated activity suggests that the Sir2 protein family represents a set of effector proteins in an evolutionarily conserved signal transduction pathway that monitors cellular energy and redox states.
Subject(s)
Fungal Proteins/physiology , Histone Deacetylases/physiology , NAD/physiology , Silent Information Regulator Proteins, Saccharomyces cerevisiae , Trans-Activators/physiology , DNA, Ribosomal/genetics , Histones/metabolism , Phylogeny , Poly(ADP-ribose) Polymerases/physiology , Recombination, Genetic , Saccharomyces cerevisiae/enzymology , Sirtuin 1 , Sirtuin 2 , SirtuinsABSTRACT
As with all metazoans, the fly makes extensive use of selective programmed cell death (PCD) to remove excess cells and properly sculpt developing tissues. Several core components of the cell death machinery have been identified in flies, including caspases and an Apaf-1 ortholog [1] [2] [3] [4]. One missing component has been a member of the Bcl-2 family of proteins, which act either pro- or anti-apoptotically as upstream regulatory proteins. Here, we report the identification of Bcl-2 family members in Drosophila - dBorg-1 (Drosophila Bcl-2 ortholog), also identified by Igaki et al. [5], and dBorg-2. Removal of dBorg-1 function during Drosophila embryonic development resulted in excess glial cells, demonstrating its pro-apoptotic function. In cell culture assays, dBorg-1 efficiently induced apoptosis but, remarkably, also demonstrated protective activity when death stimuli were introduced. Finally, ectopic expression of dBorg-1 in the eye led to subtle defects that were strongly potentiated by ultra violet (UV) irradiation, resulting in a dramatic loss of retinal cells.
Subject(s)
Apoptosis , Drosophila Proteins , Insect Proteins/physiology , Membrane Proteins/physiology , Proto-Oncogene Proteins c-bcl-2/physiology , Animals , Apoptosis/radiation effects , Base Sequence , CHO Cells , Cell Line , Cell Survival , Cricetinae , DNA, Complementary , Drosophila , Eye/cytology , Gene Expression Regulation, Developmental , Humans , Insect Proteins/genetics , Membrane Proteins/genetics , Molecular Sequence Data , Neuroglia , Proto-Oncogene Proteins c-bcl-2/genetics , Ultraviolet RaysSubject(s)
Cell Adhesion Molecules, Neuronal/physiology , Drosophila Proteins , Eye Proteins , Insect Proteins/physiology , Membrane Proteins/physiology , Photoreceptor Cells, Invertebrate/cytology , Signal Transduction/physiology , Animals , Cell Differentiation/physiology , Drosophila , Intracellular Signaling Peptides and Proteins , Receptors, NotchABSTRACT
Although silencing is a significant form of transcriptional regulation, the functional and mechanistic limits of its conservation have not yet been established. We have identified the Schizosaccharomyces pombe hst4(+) gene as a member of the SIR2/HST silencing gene family that is defined in organisms ranging from bacteria to humans. hst4Delta mutants grow more slowly than wild-type cells and have abnormal morphology and fragmented DNA. Mutant strains show decreased silencing of reporter genes at both telomeres and centromeres. hst4(+) appears to be important for centromere function as well because mutants have elevated chromosome-loss rates and are sensitive to a microtubule-destabilizing drug. Consistent with a role in chromatin structure, Hst4p localizes to the nucleus and appears concentrated in the nucleolus. hst4Delta mutant phenotypes, including growth and silencing phenotypes, are similar to those of the Saccharomyces cerevisiae HSTs, and at a molecular level, hst4(+) is most similar to HST4. Furthermore, hst4(+) is a functional homologue of S. cerevisiae HST3 and HST4 in that overexpression of hst4(+) rescues the temperature-sensitivity and telomeric silencing defects of an hst3Delta hst4Delta double mutant. These results together demonstrate that a SIR-like silencing mechanism is conserved in the distantly related yeasts and is likely to be found in other organisms from prokaryotes to mammals.
Subject(s)
Centromere/metabolism , DNA-Binding Proteins/genetics , Fungal Proteins/genetics , Gene Silencing , Histone Deacetylases , Schizosaccharomyces/genetics , Silent Information Regulator Proteins, Saccharomyces cerevisiae , Trans-Activators/genetics , Cloning, Molecular , DNA-Binding Proteins/chemistry , Fluorescent Antibody Technique , Gene Expression Regulation, Fungal , Genes, Fungal , Microscopy, Phase-Contrast , Mutation , Phenotype , Saccharomyces cerevisiae/genetics , Schizosaccharomyces/growth & development , Sequence Alignment , Sirtuin 2 , Sirtuins , Telomere/genetics , Trans-Activators/chemistryABSTRACT
Silencing is a universal form of transcriptional regulation in which regions of the genome are reversibly inactivated by changes in chromatin structure. Sir2 (Silent Information Regulator) protein is unique among the silencing factors in Saccharomyces cerevisiae because it silences the rDNA as well as the silent mating-type loci and telomeres. Discovery of a gene family of Homologues of Sir Two (HSTs) in organisms from bacteria to humans suggests that SIR2's silencing mechanism might be conserved. The Sir2 and Hst proteins share a core domain, which includes two diagnostic sequence motifs of unknown function as well as four cysteines of a putative zinc finger. We demonstrate by mutational analyses that the conserved core and each of its motifs are essential for Sir2p silencing. Chimeras between Sir2p and a human Sir2 homologue (hSir2Ap) indicate that this human protein's core can substitute for that of Sir2p, implicating the core as a silencing domain. Immunofluorescence studies reveal partially disrupted localization, accounting for the yeast-human chimeras' ability to function at only a subset of Sir2p's target loci. Together, these results support a model for the involvement of distinct Sir2p-containing complexes in HM/telomeric and rDNA silencing and that HST family members, including the widely expressed hSir2A, may perform evolutionarily conserved functions.
Subject(s)
Conserved Sequence/physiology , DNA-Binding Proteins/metabolism , Gene Expression Regulation , Histone Deacetylases , Repressor Proteins/metabolism , Saccharomyces cerevisiae/genetics , Silent Information Regulator Proteins, Saccharomyces cerevisiae , Trans-Activators/metabolism , Amino Acid Sequence , Cell Nucleus/metabolism , Chromosomes, Fungal/genetics , Conserved Sequence/genetics , Cysteine/genetics , Cysteine/metabolism , DNA, Ribosomal/genetics , DNA-Binding Proteins/chemistry , DNA-Binding Proteins/genetics , Evolution, Molecular , Genes, Dominant/genetics , Genes, Dominant/physiology , Genes, Fungal/genetics , Genes, Mating Type, Fungal , Genetic Complementation Test , Humans , Molecular Sequence Data , Mutation , RNA, Messenger/analysis , RNA, Messenger/genetics , Recombinant Fusion Proteins/chemistry , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Repressor Proteins/chemistry , Repressor Proteins/genetics , Saccharomyces cerevisiae/cytology , Saccharomyces cerevisiae/metabolism , Saccharomyces cerevisiae/physiology , Sirtuin 1 , Sirtuin 2 , Sirtuins , Structure-Activity Relationship , Telomere/genetics , Trans-Activators/chemistry , Trans-Activators/geneticsABSTRACT
Transcriptional silencing in Saccharomyces cerevisiae occurs at the silent mating-type loci HML and HMR, at telomeres, and at the ribosomal DNA (rDNA) locus RDN1. Silencing in the rDNA occurs by a novel mechanism that depends on a single Silent Information Regulator (SIR) gene, SIR2. SIR4, essential for other silenced loci, paradoxically inhibits rDNA silencing. In this study, we elucidate a regulatory mechanism for rDNA silencing based on the finding that rDNA silencing strength directly correlates with cellular Sir2 protein levels. The endogenous level of Sir2p was shown to be limiting for rDNA silencing. Furthermore, small changes in Sir2p levels altered rDNA silencing strength. In rDNA silencing phenotypes, sir2 mutations were shown to be epistatic to sir4 mutations, indicating that SIR4 inhibition of rDNA silencing is mediated through SIR2. Furthermore, rDNA silencing is insensitive to SIR3 overexpression, but is severely reduced by overexpression of full-length Sir4p or a fragment of Sir4p that interacts with Sir2p. This negative effect of SIR4 overexpression was overridden by co-overexpression of SIR2, suggesting that SIR4 directly inhibits the rDNA silencing function of SIR2. Finally, genetic manipulations of SIR4 previously shown to promote extended life span also resulted in enhanced rDNA silencing. We propose a simple model in which telomeres act as regulators of rDNA silencing by competing for limiting amounts of Sir2 protein.
Subject(s)
DNA, Ribosomal/metabolism , DNA-Binding Proteins/metabolism , Fungal Proteins/metabolism , Gene Expression Regulation, Fungal , Genes, Regulator , Histone Deacetylases , Saccharomyces cerevisiae/genetics , Silent Information Regulator Proteins, Saccharomyces cerevisiae , Trans-Activators/metabolism , Transcription, Genetic , Fungal Proteins/biosynthesis , Genes, Fungal , Genes, Mating Type, Fungal , Genotype , Models, Genetic , Phenotype , Sirtuin 2 , Sirtuins , TelomereABSTRACT
A set of yeast strains based on Saccharomyces cerevisiae S288C in which commonly used selectable marker genes are deleted by design based on the yeast genome sequence has been constructed and analysed. These strains minimize or eliminate the homology to the corresponding marker genes in commonly used vectors without significantly affecting adjacent gene expression. Because the homology between commonly used auxotrophic marker gene segments and genomic sequences has been largely or completely abolished, these strains will also reduce plasmid integration events which can interfere with a wide variety of molecular genetic applications. We also report the construction of new members of the pRS400 series of vectors, containing the kanMX, ADE2 and MET15 genes.
Subject(s)
Gene Deletion , Genetic Markers/physiology , Mutation/physiology , Plasmids/chemistry , Saccharomyces cerevisiae/genetics , Alleles , Blotting, Northern , Blotting, Southern , DNA Primers/chemistry , Gene Expression , Genome, Fungal , Plasmids/genetics , Plasmids/physiology , Polymerase Chain Reaction , Saccharomyces cerevisiae/physiologyABSTRACT
Retrotransposon Ty1 faces a formidable cell barrier during transposition--the yeast nuclear membrane which remains intact throughout the cell cycle. We investigated the mechanism by which transposition intermediates are transported from the cytoplasm (the presumed site of Ty1 DNA synthesis) to the nucleus, where they are integrated into the genome. Ty1 integrase has a nuclear localization signal (NLS) at its C terminus. Both full-length integrase and a C-terminal fragment localize to the nucleus. C-terminal deletion mutants in Ty1 integrase were used to map the putative NLS to the last 74 amino acid residues of integrase. Mutations in basic segments within this region decreased retrotransposition at least 50-fold in vivo. Furthermore, these mutant integrase proteins failed to localize to the nucleus. Production of virus-like particles, reverse transcriptase activity, and complete in vitro Ty1 integration resembled wild-type levels, consistent with failure of the mutant integrases to enter the nucleus.
Subject(s)
Integrases/physiology , Nuclear Localization Signals/physiology , Retroelements/physiology , Amino Acid Sequence , Cell Nucleus/metabolism , Molecular Sequence Data , Mutagenesis, Site-Directed , Nuclear Localization Signals/genetics , Saccharomyces cerevisiaeABSTRACT
The two-hybrid system was used to define regions of the Ty1 Gag protein responsible for multimerization. Gag truncations lacking the first 146 or the last 97 amino acids (Gag is 440 amino acids in length) interact. A severely C-terminally truncated molecule (lacking the last 207 amino acids) was the smallest truncation to interact, suggesting that some protein-protein interactions between Gag molecules are mediated through the first 233 amino acids. However, an internal deletion of amino acids 147 to 233 does not abolish Gag-Gag interaction, indicating that more than one region can mediate Gag interaction. Surprisingly, we found that a truncation lacking the last 97 amino acids interacts with itself but not with full-length Gag. This is apparently due to an artifact of the two-hybrid assay, since these same molecules coassemble with wild-type Gag into Ty1 virus-like particles.
Subject(s)
Chromosome Mapping , Gene Products, gag/genetics , Retroelements , Saccharomyces cerevisiae/genetics , Nucleic Acid Hybridization , Viral Fusion Proteins/metabolism , Virion/metabolism , Virus AssemblyABSTRACT
Cleavage of the Gag and Gag-Pol polyprotein precursors is a critical step in proliferation of retroviruses and retroelements. The Ty1 retroelement of Saccharomyces cerevisiae forms virus-like particles (VLPs) made of the Gag protein. Ty1 Gag is not obviously homologous to the Gag proteins of retroviruses. The apparent molecular mass of Gag is reduced from 58 to 54 kDa during particle maturation. Antibodies raised against the C-terminal peptide of Gag react with the 58-kDa polypeptide but not with the 54-kDa one, indicating that Gag is proteolytically processed at the C terminus. A protease cleavage site between positions 401 and 402 of the Gag precursor was defined by carboxy-terminal sequencing of the processed form of Gag. Certain deletion and substitution mutations in the C terminus of the Gag precursor result in particles that are two-thirds the diameter of the wild-type VLPs. While the Ty1 protease is active in these mutants, their transposition rates are decreased 20-fold compared with that of wild-type Ty1. Thus, the Gag C-terminal portion, released in the course of particle maturation, probably plays a significant role in VLP morphogenesis and Ty1 transposition.
Subject(s)
DNA Transposable Elements/genetics , Gene Products, gag/genetics , Saccharomyces cerevisiae/genetics , Antibodies , Base Sequence , Gene Products, gag/immunology , Gene Products, gag/metabolism , Molecular Sequence Data , Mutation , Plasmids/metabolism , Saccharomyces cerevisiae/metabolism , Virus Assembly/geneticsABSTRACT
Genomic silencing is a fundamental mechanism of transcriptional regulation, yet little is known about conserved mechanisms of silencing. We report here the discovery of four Saccharomyces cerevisiae homologs of the SIR2 silencing gene (HSTs), as well as conservation of this gene family from bacteria to mammals. At least three HST genes can function in silencing; HST1 overexpression restores transcriptional silencing to a sir2 mutant and hst3 hst4 double mutants are defective in telomeric silencing. In addition, HST3 and HST4 together contribute to proper cell cycle progression, radiation resistance, and genomic stability, establishing new connections between silencing and these fundamental cellular processes.