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1.
J Parasitol ; 98(4): 894-6, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22360588

ABSTRACT

Among acanthocephalans, eggs are typically dispersed in the feces of definitive hosts. A recent laboratory-based study provided support for the hypothesis that some female acanthocephalans (Acanthocephalus dirus) carry eggs into the environment prior to dispersal. Here, we examined the potential occurrence of this relationship under natural conditions. Using 6 field surveys, we searched the sediment of a local stream to determine whether the bodies of A. dirus females could be located. We recovered the bodies of 24 intact A. dirus individuals from the stream sediment, of which 5 were mature females. All 5 of the mature females contained mature eggs, with 1 female carrying approximately 10,000. These results are consistent with the interpretation that eggs can be dispersed from the bodies of female A. dirus in nature. We also found that there was significant variation in the number of mature eggs present in the females, with 4 of the 5 females carrying fewer than 400 mature eggs. In addition, we recovered approximately 20,000 mature eggs from a fecal pellet that had been expelled from a fish. We propose that eggs may be dispersed both in the feces of definitive hosts and from the bodies of expelled female A. dirus under natural conditions.


Subject(s)
Acanthocephala/physiology , Fish Diseases/parasitology , Helminthiasis, Animal/parasitology , Acanthocephala/isolation & purification , Animals , Feces/parasitology , Female , Fish Diseases/transmission , Fishes , Geologic Sediments/parasitology , Helminthiasis, Animal/transmission , Isopoda/parasitology , Male , Ovum/physiology , Parasite Egg Count/veterinary , Rivers/parasitology , Seasons
2.
Oncogene ; 31(45): 4789-97, 2012 Nov 08.
Article in English | MEDLINE | ID: mdl-22266850

ABSTRACT

Mdm2 is the major negative regulator of p53 tumor-suppressor activity. This oncoprotein is overexpressed in many human tumors that retain the wild-type p53 allele. As such, targeted inhibition of Mdm2 is being considered as a therapeutic anticancer strategy. The N-terminal hydrophobic pocket of Mdm2 binds to p53 and thereby inhibits the transcription of p53 target genes. Additionally, the C-terminus of Mdm2 contains a RING domain with intrinsic ubiquitin E3 ligase activity. By recruiting E2 ubiquitin-conjugating enzyme(s), Mdm2 acts as a molecular scaffold to facilitate p53 ubiquitination and proteasome-dependent degradation. Mdmx (Mdm4), an Mdm2 homolog, also has a RING domain and hetero-oligomerizes with Mdm2 to stimulate its E3 ligase activity. Recent studies have shown that C-terminal residues adjacent to the RING domain of both Mdm2 and Mdmx contribute to Mdm2 E3 ligase activity. However, the molecular mechanisms mediating this process remain unclear, and the biological consequences of inhibiting Mdm2/Mdmx co-operation or blocking Mdm2 ligase function are relatively unexplored. This study presents biochemical and cell biological data that further elucidate the mechanisms by which Mdm2 and Mdmx co-operate to regulate p53 level and activity. We use chemical and genetic approaches to demonstrate that functional inhibition of Mdm2 ubiquitin ligase activity is insufficient for p53 activation. This unexpected result suggests that concomitant treatment with Mdm2/Mdmx antagonists may be needed to achieve therapeutic benefit.


Subject(s)
Neoplasms/metabolism , Proto-Oncogene Proteins c-mdm2/metabolism , Cell Cycle Proteins , Cell Line, Tumor , Cell Survival/genetics , Gene Expression , Humans , Imidazoles/pharmacology , Mutation , Neoplasms/genetics , Nuclear Proteins/metabolism , Piperazines/pharmacology , Protein Binding/drug effects , Protein Processing, Post-Translational , Protein Stability , Proto-Oncogene Proteins/metabolism , Proto-Oncogene Proteins c-mdm2/antagonists & inhibitors , Proto-Oncogene Proteins c-mdm2/genetics , Transcriptional Activation , Tumor Suppressor Protein p53/metabolism , Ubiquitination
3.
Cell Death Differ ; 13(6): 973-83, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16575406

ABSTRACT

P53 is a transcription factor that can cause cells to be eliminated by apoptosis or senescent-like arrest upon its activation by irreparable genetic damage, excessively expressed oncogenes, or a broad spectrum of other stresses. As P53 executes life and death decisions, its activity must be stringently regulated, which implies that it is not likely to be controlled by a simple regulatory mechanism involving a binary on-off switch. This brief review will summarize a subset of the new information presented at the 10th P53 workshop in Dunedin, New Zealand in November 2004 as well as very recent publications that provide new insights into the molecular regulators of P53. Data emerging from mouse models provide a fundamentally different view of how P53 is regulated than suggested by more traditional in vitro approaches. The differences between cell culture and mouse models demonstrate the importance of preserving stoichiometric relationships between P53 and its various regulators to obtain an accurate view of the relevant molecular mechanisms that control P53 activity.


Subject(s)
Apoptosis Regulatory Proteins/metabolism , DNA/metabolism , Protein Processing, Post-Translational , Proto-Oncogene Proteins/metabolism , Animals , Antineoplastic Agents/pharmacology , Apoptosis Regulatory Proteins/chemistry , Apoptosis Regulatory Proteins/genetics , Cell Cycle Proteins/genetics , Cell Cycle Proteins/metabolism , Cell Transformation, Neoplastic/genetics , Cell Transformation, Neoplastic/metabolism , DNA/genetics , Mice , Models, Genetic , Mutation , Proline/chemistry , Promoter Regions, Genetic/genetics , Protein Structure, Tertiary , Proto-Oncogene Proteins/chemistry , Proto-Oncogene Proteins/genetics , Proto-Oncogene Proteins c-mdm2/antagonists & inhibitors , Proto-Oncogene Proteins c-mdm2/genetics , Proto-Oncogene Proteins c-mdm2/metabolism , Transcriptional Activation
4.
Curr Top Microbiol Immunol ; 302: 169-203, 2006.
Article in English | MEDLINE | ID: mdl-16620029

ABSTRACT

The c-myc oncogene acts as a pluripotent modulator of transcription during normal cell growth and proliferation. Deregulated c-myc activity in cancer can lead to excessive activation of its downstream pathways, and may also stimulate changes in gene expression and cellular signaling that are not observed under non-pathological conditions. Under certain conditions, aberrant c-myc activity is associated with the appearance of DNA damage-associated markers and karyotypic abnormalities. In this chapter, we discuss mechanisms by which c-myc may be directly or indirectly associated with the induction of genomic instability. The degree to which c-myc-induced genomic instability influences the initiation or progression of cancer is likely to depend on other factors, which are discussed herein.


Subject(s)
Genes, myc , Genomic Instability , Neoplasms/etiology , Neoplasms/genetics , Animals , Cell Cycle , DNA Damage , DNA Repair , Gene Expression Regulation , Humans , Models, Biological , Neoplasms/metabolism , Oncogenes , Oncogenic Viruses/pathogenicity , Reactive Oxygen Species/metabolism
5.
Mol Cell Biol ; 21(10): 3576-88, 2001 May.
Article in English | MEDLINE | ID: mdl-11313483

ABSTRACT

The Epstein-Barr virus (EBV) replicates once per cell cycle and segregates with high efficiency yet does not encode the enzymes needed for DNA replication or the proteins required to contact mitotic spindles. The virus-encoded EBNA-1 (EBV nuclear antigen 1) and latent replication origin (oriP) are required for both replication and segregation. We developed a sensitive and specific fluorescent labeling strategy to analyze the interactions of both EBNA-1 with viral episomes and viral episomes with host chromosomes. This enabled investigation of the hypothesis that replication and chromosome tethering are linked through the EBNA-1 protein. We show that deleting EBNA-1 or oriP disrupts mitotic chromosome tethering but removing the dyad symmetry element of oriP does not. Microscopic and biochemical approaches demonstrated that an EBNA-1 mutant lacking residues 16 to 372 bound to oriP plasmids but did not support their mitotic chromosome association and that the mutant lost the ability of wild-type EBNA-1 to associate with interphase chromatin. Importantly, the transient-replication abilities of various mutant forms of EBV plasmids, including the mutant form with the EBNA-1 internal deletion, correlated directly with their chromosome-tethering abilities. These data lead us to propose that EBNA-1 recruits oriP-containing plasmids into chromatin subdomains in interphase nuclei to both engage the host replication machinery and enable the plasmids to adhere to host chromosomes to increase their segregation efficiency.


Subject(s)
Herpesvirus 4, Human/physiology , Virus Replication , Chromosomes , Epstein-Barr Virus Nuclear Antigens/genetics , HeLa Cells , Humans , Mutation , Plasmids
6.
J Cell Sci ; 114(Pt 1): 49-58, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11112689

ABSTRACT

Mitotic chromosome segregation is mediated by spindle microtubules attached to centromeres. Recent studies, however, revealed that acentric DNA molecules, such as viral replicons and double minute chromosomes, can efficiently segregate into daughter cells by associating with mitotic chromosomes. Based on this similarity between viral and cellular acentric molecules, we introduced Epstein-Barr virus vectors into cells harboring double minute chromosomes and compared their mitotic behaviors. We added lac operator repeats to an Epstein-Barr virus vector, which enabled us to readily identify the transgene in cells expressing a fusion protein between the lac repressor and green fluorescent protein. Unexpectedly, we found that Epstein-Barr virus vectors integrated into the acentric double minute chromosomes, but not into normal chromosomes, in all of the six stably transfected clones examined. While transiently transfected Epstein-Barr virus vectors randomly associated with wheel-shaped prometaphase chromosome rosettes, the chimeras of double minute chromosomes and Epstein-Barr virus vectors in stably transfected clones always attached to the periphery of chromosome rosettes. These chimeric acentric molecules faithfully represented the behavior of native double minute chromosomes, providing a tool for analyzing their behavior in living cells throughout the cell cycle. Further detailed analyses, including real-time observations, revealed that double minute chromosomes appeared to be repelled from the spindle poles at the same time that they attached to the chromosome periphery, while centromeric regions were pulled poleward by the attached microtubules. Disrupting microtubule organization eliminated such peripheral localization of double minute chromosomes, but it did not affect their association with chromosomes. The results suggest a model in which double minute chromosomes, but not Epstein-Barr virus vectors, are subject to the microtubule-mediated antipolar force, while they both employ chromosome tethering strategies to increase their segregation to daughter cells.


Subject(s)
Chromosome Segregation/physiology , Mitosis/physiology , Centromere/physiology , Genetic Vectors/genetics , Herpesvirus 4, Human/genetics , Humans , Metaphase/physiology , Microtubules/drug effects , Microtubules/metabolism , Tumor Cells, Cultured , Vinblastine/pharmacology , Virus Integration
7.
Nat Cell Biol ; 3(12): E277-86, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11781586

ABSTRACT

The cellular response to ionizing radiation provides a conceptual framework for understanding how a yeast checkpoint system, designed to make binary decisions between arrest and cycling, evolved in a way as to allow reversible arrest, senescence or apoptosis in mammals. We propose that the diversity of responses to ionizing radiation in mammalian cells is possible because of the addition of a new regulatory control module involving the tumour-suppressor gene p53. We review the complex mechanisms controlling p53 activity and discuss how the p53 regulatory module enables cells to grow, arrest or die by integrating DNA damage checkpoint signals with the response to normal mitogenic signalling and the aberrant signalling engendered by oncogene activation.


Subject(s)
DNA Damage/physiology , Evolution, Molecular , Tumor Suppressor Protein p53/physiology , Yeasts/physiology
8.
Nat Genet ; 26(1): 37-43, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10973245

ABSTRACT

The gene Trp53 is among the most frequently mutated and studied genes in human cancer, but the mechanisms by which it suppresses tumour formation remain unclear. We generated mice with an allele encoding changes at Leu25 and Trp26, known to be essential for transcriptional transactivation and Mdm2 binding, to enable analyses of Trp53 structure and function in vivo. The mutant Trp53 was abundant, its level was not affected by DNA damage and it bound DNA constitutively; however, it showed defects in cell-cycle regulation and apoptosis. Both mutant and Trp53-null mouse embryonic fibroblasts (MEFs) were readily transformed by oncogenes, and the corresponding mice were prone to tumours. We conclude that the determining pathway for Trp53 tumour-suppressor function in mice requires the transactivation domain.


Subject(s)
Gene Expression Regulation, Neoplastic , Genes, p53 , Transcriptional Activation , Tumor Suppressor Protein p53 , Alleles , Animals , Apoptosis/genetics , DNA Damage/drug effects , Dactinomycin/pharmacology , Female , Mice , Mice, Transgenic , Models, Animal , Neoplasm Transplantation , Nucleic Acid Synthesis Inhibitors/pharmacology , Tumor Suppressor Protein p14ARF , Tumor Suppressor Protein p53/chemistry , Tumor Suppressor Protein p53/genetics , Tumor Suppressor Protein p53/metabolism
9.
Proc Natl Acad Sci U S A ; 97(7): 3266-71, 2000 Mar 28.
Article in English | MEDLINE | ID: mdl-10716710

ABSTRACT

p19ARF has been implicated as a key regulator of p53 stability and activation. While numerous stresses activate the p53 growth arrest pathway, those requiring p19ARF remain to be elucidated. We used p19ARF knockout mouse embryo fibroblasts to show that DNA damage and microtubule disruption require p19ARF to induce p53 responses, whereas ribonucleotide depletion and inhibition of RNA synthesis by low doses of actinomycin D do not. The data provide evidence that the arrest pathway activated by ribonucleotide depletion involves some different signal transducers than those activated by DNA damage or microtubule disruption. We also present biochemical analyses that provide insights into the mechanism by which p53 and p19ARF cooperate in normal cells to induce cell cycle arrest.


Subject(s)
DNA Damage , Microtubules/drug effects , Proteins/metabolism , Ribonucleotides/metabolism , Tumor Suppressor Protein p53/metabolism , Animals , Blotting, Western , Cells, Cultured , Mice , Mice, Knockout , Nocodazole/pharmacology , Polyploidy , Tumor Suppressor Protein p14ARF
10.
J Cell Biochem Suppl ; Suppl 35: 107-14, 2000.
Article in English | MEDLINE | ID: mdl-11389539

ABSTRACT

Autonomous replicons, such as viral episomes and oncogene containing double minute chromosomes (DMs), lack centromeres and consequently should be lost rapidly when the nuclear membrane breaks down at mitosis. Surprisingly, they are not. This raises the important question of the mechanisms that enable their efficient transmission to daughter cells. We review recent developments in GFP-based chromosome labeling strategies that enable real time analyses using high resolution light microscopy to provide insights into this issue. The results reveal that episomes and DMs both adhere to host chromosomes, a process referred to as "chromosome tethering". Such association enables acentric molecules to use the chromosomal centromere in trans, thereby achieving efficient transmission to daughter cells. This unique mechanism of mitotic segregation also raises the possibility of developing a new class of anti-cancer drugs that work by selectively eliminating growth enhancing genes from cancer cells. J. Cell. Biochem. Suppl. 35:107-114, 2000.


Subject(s)
Centromere/physiology , Chromosomes/metabolism , Luminescent Proteins/metabolism , Microscopy, Fluorescence/methods , Neoplasms/metabolism , Animals , Cell Nucleus/metabolism , Green Fluorescent Proteins , Humans , Mitosis , Models, Biological
11.
Clin Immunol ; 93(3): 198-208, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10600330

ABSTRACT

Leflunomide (Arava) has recently been approved by the Food and Drug Administration for the treatment of rheumatoid arthritis (RA). This approval was based on data from a double-blind, multicenter trials in the United States (leflunomide versus methotrexate versus placebo) in which leflunomide was superior to placebo and similar to methotrexate (Strand et al., Arch. Intern. Med., in press, 1999). In a multicenter European trial, leflunomide was similar to sulfasalazine in efficacy and side effects (Smolen et al., Lancet 353, 259-266, 1999). Both methotrexate and leflunomide retarded the rate of radiolographic progression, entitling them to qualify as disease-modifying agents (Strand et al., Arch. Intern. Med., in press, 1999). Leflunomide is an immunomodulatory drug that may exert its effects by inhibiting the mitochondrial enzyme dihydroorotate dehydrogenase (DHODH), which plays a key role in the de novo synthesis of the pyrimidine ribonucleotide uridine monophosphate (rUMP). The inhibition of human DHODH by A77 1726, the active metabolite of leflunomide, occurs at levels (approximately 600 nM) that are achieved during treatment of RA. We propose that leflunomide prevents the expansion of activated and autoimmune lymphocytes by interfering with the cell cycle progression due to inadequate production of rUMP and utilizing mechanisms involving p53. The relative lack of toxicity of A77 1726 on nonlymphoid cells may be due to the ability of these cells to fulfill their ribonucleotide requirements by use of salvage pyrimidine pathway, which makes them less dependent on de novo synthesis.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Arthritis, Rheumatoid/drug therapy , Isoxazoles/therapeutic use , Animals , Enzyme Inhibitors/therapeutic use , Humans , Leflunomide
12.
Nature ; 400(6739): 81-3, 1999 Jul 01.
Article in English | MEDLINE | ID: mdl-10403253

ABSTRACT

Damage to DNA in the cell activates the tumour-suppressor protein p53, and failure of this activation leads to genetic instability and a predisposition to cancer. It is therefore crucial to understand the signal transduction mechanisms that connect DNA damage with p53 activation. The enzyme known as DNA-dependent protein kinase (DNA-PK) has been proposed to be an essential activator of p53, but the evidence for its involvement in this pathway is controversial. We now show that the p53 response is fully functional in primary mouse embryonic fibroblasts lacking DNA-PK: irradiation-induced DNA damage in these defective fibroblasts induces a normal response of p53 accumulation, phosphorylation of a p53 serine residue at position 15, nuclear localization and binding to DNA of p53. The upregulation of p53-target genes and cell-cycle arrest also occur normally. The DNA-PK-deficient cell line SCGR11 contains a homozygous mutation in the DNA-binding domain of p53, which may explain the defective response by p53 reported in this line. Our results indicate that DNA-PK activity is not required for cells to mount a p53-dependent response to DNA damage.


Subject(s)
DNA Damage , DNA-Binding Proteins , Protein Serine-Threonine Kinases/metabolism , Tumor Suppressor Protein p53/metabolism , Animals , Cell Line , Cell Nucleus/metabolism , Cricetinae , DNA/metabolism , DNA Repair , DNA-Activated Protein Kinase , Mice , Molecular Sequence Data , Mutation , Phosphorylation , Protein Binding , Protein Serine-Threonine Kinases/genetics , Signal Transduction , Tumor Suppressor Protein p53/genetics
13.
EMBO J ; 18(6): 1660-72, 1999 Mar 15.
Article in English | MEDLINE | ID: mdl-10075936

ABSTRACT

Appropriate subcellular localization is crucial for regulating p53 function. We show that p53 export is mediated by a highly conserved leucine-rich nuclear export signal (NES) located in its tetramerization domain. Mutation of NES residues prevented p53 export and hampered tetramer formation. Although the p53-binding protein MDM2 has an NES and has been proposed to mediate p53 export, we show that the intrinsic p53 NES is both necessary and sufficient for export. This report also demonstrates that the cytoplasmic localization of p53 in neuroblastoma cells is due to its hyperactive nuclear export: p53 in these cells can be trapped in the nucleus by the export-inhibiting drug leptomycin B or by binding a p53-tetramerization domain peptide that masks the NES. We propose a model in which regulated p53 tetramerization occludes its NES, thereby ensuring nuclear retention of the DNA-binding form. We suggest that attenuation of p53 function involves the conversion of tetramers into monomers or dimers, in which the NES is exposed to the proteins which mediate their export to the cytoplasm.


Subject(s)
Tumor Suppressor Protein p53/chemistry , Tumor Suppressor Protein p53/metabolism , 3T3 Cells , Amino Acid Sequence , Animals , Cattle , Conserved Sequence , HeLa Cells , Humans , Leucine , Macromolecular Substances , Mice , Models, Molecular , Mutagenesis, Site-Directed , Neuroblastoma , Osteosarcoma , Protein Structure, Secondary , Rabbits , Recombinant Proteins/biosynthesis , Recombinant Proteins/chemistry , Sequence Alignment , Signal Transduction , Subcellular Fractions/metabolism , Transfection , Tumor Cells, Cultured , Tumor Suppressor Protein p53/genetics , Xenopus , Zebrafish
14.
Nat Genet ; 21(1): 111-4, 1999 Jan.
Article in English | MEDLINE | ID: mdl-9916802

ABSTRACT

Expression of the human telomerase catalytic component, hTERT, in normal human somatic cells can reconstitute telomerase activity and extend their replicative lifespan. We report here that at twice the normal number of population doublings, telomerase-expressing human skin fibroblasts (BJ-hTERT) and retinal pigment epithelial cells (RPE-hTERT) retain normal growth control in response to serum deprivation, high cell density, G1 or G2 phase blockers and spindle inhibitors. In addition, we observed no cell growth in soft agar and detected no tumour formation in vivo. Thus, we find that telomerase expression in normal cells does not appear to induce changes associated with a malignant phenotype.


Subject(s)
Cell Transformation, Neoplastic , Protein Biosynthesis , RNA , Telomerase/biosynthesis , Aspartic Acid/analogs & derivatives , Aspartic Acid/pharmacology , Cell Line , Cell Line, Transformed , Cyclin-Dependent Kinase Inhibitor p16/metabolism , DNA-Binding Proteins , Enzyme Inhibitors/pharmacology , Humans , Hydroxyurea/pharmacology , Nucleic Acid Synthesis Inhibitors/pharmacology , Phenotype , Phosphonoacetic Acid/analogs & derivatives , Phosphonoacetic Acid/pharmacology , Phosphorylation , Proteins/genetics , Retinoblastoma Protein/metabolism , Telomerase/genetics , Tumor Cells, Cultured
15.
Oncogene ; 18(53): 7656-65, 1999 Dec 13.
Article in English | MEDLINE | ID: mdl-10618705

ABSTRACT

p53 activation by diverse stresses involves post-translational modifications that alter its structure and result in its nuclear accumulation. We will discuss several unresolved topics regarding p53 regulation which are currently under investigation. DNA damage is perhaps the best-studied stress which activates p53, and recent data implicate phosphorylation at N-terminal serine residues as critical in this process. We discuss recent data regarding the potential kinases which modify p53 and the possible role of the resulting phosphorylation events. By contrast, much less is understood about agents which disrupt the mitotic spindle. The cell cycle phase, induction signal, and biochemical mechanism of the reversible arrest induced by microtubule disruption are currently under investigation. Finally, a key event in response to any genotoxic stress is the accumulation of p53 in the nucleus. The factors which determine the steady state level of p53 are starting to be elucidated, but the mechanisms responsible for nuclear accumulation and nuclear export remain controversial. We discuss new studies revealing a mechanism for nuclear retention of p53, and the potential contributions of MDM2 to this process.


Subject(s)
Cell Nucleus/metabolism , DNA Damage/physiology , Protein Processing, Post-Translational , Tumor Suppressor Protein p53/metabolism , Animals , DNA Damage/genetics , G1 Phase , Humans , Microtubules/metabolism , Phosphorylation
16.
BioDrugs ; 12(4): 301-15, 1999 Oct.
Article in English | MEDLINE | ID: mdl-18031184

ABSTRACT

Leflunomide has recently been approved by the US Food and Drug Administration for the treatment of rheumatoid arthritis. This approval was based on data from double-blind multicentre trials in the US (US 301; leflunomide versus methotrexate versus placebo) and multicentre European trials (leflunomide versus sulfasalazine versus placebo, and leflunomide versus methotrexate versus placebo). In these trials, leflunomide was superior to placebo and similar to methotrexate or sulfasalazine in efficacy and adverse effects. Both methotrexate and leflunomide retarded the rate of radiological progression, entitling them to qualify as disease-modifying agents (DMARDs). Leflunomide is an immunomodulatory drug that may exert its effects by inhibiting the mitochondrial enzyme dihydro-orotate dehydrogenase (DHO-DH), which plays a key role in the de novo synthesis of the pyrimidine ribonucleotide uridine monophosphate (rUMP). The inhibition of human DHO-DH by A77-1726, the active metabolite of leflunomide, occurs at concentrations (approximately 600 nmol/L) that are achieved during treatment of rheumatoid arthritis. We propose that leflunomide prevents the expansion of activated and autoimmune lymphocytes by interfering with cell cycle progression. This is mediated by inadequate production of rUMP and utilises mechanisms involving the sensor protein p53. The relative lack of toxicity of A77-1726 on nonlymphoid cells may be due to the ability of these cells to fulfil their ribonucleotide requirements by use of the salvage pyrimidine pathway, which makes them less dependent on de novo synthesis.

17.
Science ; 281(5379): 1005-9, 1998 Aug 14.
Article in English | MEDLINE | ID: mdl-9703500

ABSTRACT

The timing and localization of DNA replication initiation in mammalian cells are heritable traits, but it is not known whether initiation requires specific DNA sequences. A site-specific recombination strategy was used to show that DNA sequences previously identified as replication initiation sites could initiate replication when transferred to new chromosomal locations. An 8-kilobase DNA sequence encompassing the origin of DNA replication in the human beta-globin locus initiated replication in the simian genome. Specific deletions within the globin origin did not initiate replication in these chromosomal sites. These data suggest that initiation of DNA replication in mammalian cells requires specific sequence information and extend the replicon hypothesis to higher eukaryotes.


Subject(s)
DNA Replication , Globins/genetics , Replication Origin , Viral Proteins , Animals , Cell Line , Chlorocebus aethiops , DNA/genetics , DNA Nucleotidyltransferases/metabolism , Gene Targeting , Humans , Integrases/metabolism , Polymerase Chain Reaction , S Phase , Sequence Deletion
18.
Curr Biol ; 8(7): 377-85, 1998 Mar 26.
Article in English | MEDLINE | ID: mdl-9545195

ABSTRACT

BACKGROUND: The amplification of oncogenes in cancer cells is often mediated by paired acentric chromatin bodies called double minute chromosomes (DMs), which can accumulate to a high copy number because of their autonomous replication during the DNA synthesis phase of the cell cycle and their subsequent uneven distribution to daughter cells during mitosis. The mechanisms that control DM segregation have been difficult to investigate, however, as the direct visualization of DMs in living cells has been precluded because they are far smaller than normal chromosomes. We have visualized DMs by developing a highly sensitive method for observing chromosome dynamics in living cells. RESULTS: The human histone H2B gene was fused to the gene encoding the green fluorescent protein (GFP) of Aequorea victoria and transfected into human HeLa cells to generate a stable line constitutively expressing H2B-GFP. The H2B-GFP fusion protein was incorporated into nucleosomes without affecting cell cycle progression. Using confocal microscopy, H2B-GFP allowed high-resolution imaging of both mitotic chromosomes and interphase chromatin, and the latter revealed various chromatin condensation states in live cells. Using H2B-GFP, we could directly observe DMs in living cancer cells; DMs often clustered during anaphase, and could form chromosomal 'bridges' between segregating daughter chromosomes. Cytokinesis severed DM bridges, resulting in the uneven distribution of DMs to daughter cells. CONCLUSIONS: The H2B-GFP system allows the high-resolution imaging of chromosomes, including DMs, without compromising nuclear and chromosomal structures and has revealed the distinctive clustering behavior of DMs in mitotic cells which contributes to their asymmetric distribution to daughter cells.


Subject(s)
Chromosomes, Human/metabolism , Chromosomes, Human/ultrastructure , Histones , Luminescent Proteins , Animals , Base Sequence , Cell Cycle , DNA Primers/genetics , Gene Expression , Genetic Vectors , Green Fluorescent Proteins , HeLa Cells , Histones/genetics , Histones/metabolism , Humans , Luminescent Proteins/genetics , Luminescent Proteins/metabolism , Microscopy, Confocal , Nucleosomes/metabolism , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Transfection
19.
Mol Cell Biol ; 18(5): 3089-100, 1998 May.
Article in English | MEDLINE | ID: mdl-9566927

ABSTRACT

Amplification of genes involved in signal transduction and cell cycle control occurs in a significant fraction of human cancers. Loss of p53 function has been proposed to enable cells with gene amplification to arise spontaneously during growth in vitro. However, this conclusion derives from studies employing the UMP synthesis inhibitor N-phosphonacetyl-L-aspartate (PALA), which, in addition to selecting for cells containing extra copies of the CAD locus, enables p53-deficient cells to enter S phase and acquire the DNA breaks that initiate the amplification process. Thus, it has not been possible to determine if gene amplification occurs spontaneously or results from the inductive effects of the selective agent. The studies reported here assess whether p53 deficiency leads to spontaneous genetic instability by comparing cell cycle responses and amplification frequencies of the human fibrosarcoma cell line HT1080 when treated with PALA or with methotrexate, an antifolate that, under the conditions used, should not generate DNA breaks. p53-deficient HT1080 cells generated PALA-resistant variants containing amplified CAD genes at a frequency of >10(-5). By contrast, methotrexate selection did not result in resistant cells at a detectable frequency (<10(-9)). However, growth of HT1080 cells under conditions that induced DNA breakage prior to selection generated methotrexate-resistant clones containing amplified dihydrofolate reductase sequences at a high frequency. These data demonstrate that, under standard growth conditions, p53 loss is not sufficient to enable cells to produce the DNA breaks that initiate amplification. We propose that p53-deficient cells must proceed through S phase under conditions that induce DNA breakage for genetic instability to occur.


Subject(s)
DNA Damage , Fibrosarcoma/pathology , Gene Amplification , Tetrahydrofolate Dehydrogenase/genetics , Tumor Suppressor Protein p53/deficiency , Aspartic Acid/analogs & derivatives , Aspartic Acid/pharmacology , Cell Cycle , Cell Cycle Proteins/metabolism , Drug Resistance , Humans , Methotrexate/pharmacology , Models, Genetic , Nucleotides/deficiency , Phosphonoacetic Acid/analogs & derivatives , Phosphonoacetic Acid/pharmacology , Selection, Genetic , Skin Neoplasms/pathology , Tumor Cells, Cultured
20.
J Cell Biol ; 140(6): 1307-20, 1998 Mar 23.
Article in English | MEDLINE | ID: mdl-9508765

ABSTRACT

Acentric, autonomously replicating extrachromosomal structures called double-minute chromosomes (DMs) frequently mediate oncogene amplification in human tumors. We show that DMs can be removed from the nucleus by a novel micronucleation mechanism that is initiated by budding of the nuclear membrane during S phase. DMs containing c-myc oncogenes in a colon cancer cell line localized to and replicated at the nuclear periphery. Replication inhibitors increased micronucleation; cell synchronization and bromodeoxyuridine-pulse labeling demonstrated de novo formation of buds and micronuclei during S phase. The frequencies of S-phase nuclear budding and micronucleation were increased dramatically in normal human cells by inactivating p53, suggesting that an S-phase function of p53 minimizes the probability of producing the broken chromosome fragments that induce budding and micronucleation. These data have implications for understanding the behavior of acentric DNA in interphase nuclei and for developing chemotherapeutic strategies based on this new mechanism for DM elimination.


Subject(s)
Cell Nucleus/genetics , DNA, Neoplasm/metabolism , Extrachromosomal Inheritance/physiology , S Phase/genetics , Antimetabolites , Bromodeoxyuridine , Cell Nucleus/pathology , Humans , In Situ Hybridization, Fluorescence , Neuroendocrine Tumors , Replicon/physiology , Tumor Cells, Cultured/cytology , Tumor Cells, Cultured/physiology , Tumor Suppressor Protein p53/physiology
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