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1.
Nat Commun ; 15(1): 3490, 2024 Apr 25.
Article in English | MEDLINE | ID: mdl-38664429

ABSTRACT

Congenital nucleotide excision repair (NER) deficiency gives rise to several cancer-prone and/or progeroid disorders. It is not understood how defects in the same DNA repair pathway cause different disease features and severity. Here, we show that the absence of functional ERCC1-XPF or XPG endonucleases leads to stable and prolonged binding of the transcription/DNA repair factor TFIIH to DNA damage, which correlates with disease severity and induces senescence features in human cells. In vivo, in C. elegans, this prolonged TFIIH binding to non-excised DNA damage causes developmental arrest and neuronal dysfunction, in a manner dependent on transcription-coupled NER. NER factors XPA and TTDA both promote stable TFIIH DNA binding and their depletion therefore suppresses these severe phenotypical consequences. These results identify stalled NER intermediates as pathogenic to cell functionality and organismal development, which can in part explain why mutations in XPF or XPG cause different disease features than mutations in XPA or TTDA.


Subject(s)
Caenorhabditis elegans , DNA Damage , DNA Repair , DNA-Binding Proteins , Endonucleases , Transcription Factor TFIIH , Caenorhabditis elegans/metabolism , Caenorhabditis elegans/genetics , Humans , Animals , Transcription Factor TFIIH/metabolism , Transcription Factor TFIIH/genetics , DNA-Binding Proteins/metabolism , DNA-Binding Proteins/genetics , Endonucleases/metabolism , Endonucleases/genetics , Caenorhabditis elegans Proteins/metabolism , Caenorhabditis elegans Proteins/genetics , Xeroderma Pigmentosum Group A Protein/metabolism , Xeroderma Pigmentosum Group A Protein/genetics , Protein Binding , Transcription Factors/metabolism , Transcription Factors/genetics , Mutation , Nuclear Proteins/metabolism , Nuclear Proteins/genetics
2.
Nat Cell Biol ; 26(5): 770-783, 2024 May.
Article in English | MEDLINE | ID: mdl-38600236

ABSTRACT

DNA-protein crosslinks (DPCs) arise from enzymatic intermediates, metabolism or chemicals like chemotherapeutics. DPCs are highly cytotoxic as they impede DNA-based processes such as replication, which is counteracted through proteolysis-mediated DPC removal by spartan (SPRTN) or the proteasome. However, whether DPCs affect transcription and how transcription-blocking DPCs are repaired remains largely unknown. Here we show that DPCs severely impede RNA polymerase II-mediated transcription and are preferentially repaired in active genes by transcription-coupled DPC (TC-DPC) repair. TC-DPC repair is initiated by recruiting the transcription-coupled nucleotide excision repair (TC-NER) factors CSB and CSA to DPC-stalled RNA polymerase II. CSA and CSB are indispensable for TC-DPC repair; however, the downstream TC-NER factors UVSSA and XPA are not, a result indicative of a non-canonical TC-NER mechanism. TC-DPC repair functions independently of SPRTN but is mediated by the ubiquitin ligase CRL4CSA and the proteasome. Thus, DPCs in genes are preferentially repaired in a transcription-coupled manner to facilitate unperturbed transcription.


Subject(s)
DNA Helicases , DNA Repair Enzymes , DNA Repair , Poly-ADP-Ribose Binding Proteins , Proteolysis , RNA Polymerase II , Transcription, Genetic , DNA Repair Enzymes/metabolism , DNA Repair Enzymes/genetics , Humans , Poly-ADP-Ribose Binding Proteins/metabolism , Poly-ADP-Ribose Binding Proteins/genetics , DNA Helicases/metabolism , DNA Helicases/genetics , RNA Polymerase II/metabolism , RNA Polymerase II/genetics , Ubiquitin-Protein Ligases/metabolism , Ubiquitin-Protein Ligases/genetics , DNA-Binding Proteins/metabolism , DNA-Binding Proteins/genetics , DNA/metabolism , DNA/genetics , HEK293 Cells , Transcription Factors/metabolism , Transcription Factors/genetics , DNA Damage , Proteasome Endopeptidase Complex/metabolism , Carrier Proteins , Receptors, Interleukin-17
3.
Nucleic Acids Res ; 51(18): e93, 2023 Oct 13.
Article in English | MEDLINE | ID: mdl-37522336

ABSTRACT

Transcription-coupled nucleotide excision repair (TC-NER) is an important DNA repair mechanism that protects against the negative effects of transcription-blocking DNA lesions. Hereditary TC-NER deficiencies cause pleiotropic and often severe neurodegenerative and progeroid symptoms. While multiple assays have been developed to determine TC-NER activity for clinical and research purposes, monitoring TC-NER is hampered by the low frequency of repair events occurring in transcribed DNA. 'Recovery of RNA Synthesis' is widely used as indirect TC-NER assay based on the notion that lesion-blocked transcription only resumes after successful TC-NER. Here, we show that measuring novel synthesis of a protein after its compound-induced degradation prior to DNA damage induction is an equally effective but more versatile manner to indirectly monitor DNA repair activity in transcribed genes. This 'Recovery of Protein Synthesis' (RPS) assay can be adapted to various degradable proteins and readouts, including imaging and immunoblotting. Moreover, RPS allows real-time monitoring of TC-NER activity in various living cells types and even in differentiated tissues of living organisms. To illustrate its utility, we show that DNA repair in transcribed genes declines in aging muscle tissue of C. elegans. Therefore, the RPS assay constitutes an important novel clinical and research tool to investigate transcription-coupled DNA repair.


Subject(s)
Caenorhabditis elegans , DNA Repair , Protein Biosynthesis , Transcription, Genetic , Animals , Caenorhabditis elegans/physiology , DNA/metabolism , DNA Damage , Aging/metabolism , Muscles/metabolism
4.
Commun Biol ; 4(1): 1336, 2021 11 25.
Article in English | MEDLINE | ID: mdl-34824371

ABSTRACT

The 10-subunit TFIIH complex is vital to transcription and nucleotide excision repair. Hereditary mutations in its smallest subunit, TTDA/GTF2H5, cause a photosensitive form of the rare developmental disorder trichothiodystrophy. Some trichothiodystrophy features are thought to be caused by subtle transcription or gene expression defects. TTDA/GTF2H5 knockout mice are not viable, making it difficult to investigate TTDA/GTF2H5 in vivo function. Here we show that deficiency of C. elegans TTDA ortholog GTF-2H5 is, however, compatible with life, in contrast to depletion of other TFIIH subunits. GTF-2H5 promotes TFIIH stability in multiple tissues and is indispensable for nucleotide excision repair, in which it facilitates recruitment of TFIIH to DNA damage. Strikingly, when transcription is challenged, gtf-2H5 embryos die due to the intrinsic TFIIH fragility in absence of GTF-2H5. These results support the idea that TTDA/GTF2H5 mutations cause transcription impairment underlying trichothiodystrophy and establish C. elegans as model for studying pathogenesis of this disease.


Subject(s)
Caenorhabditis elegans Proteins/genetics , Caenorhabditis elegans/physiology , DNA Repair/genetics , DNA, Helminth/physiology , Transcription Factors/genetics , Animals , Caenorhabditis elegans/genetics , Caenorhabditis elegans Proteins/metabolism , Transcription Factors/metabolism
5.
Front Cell Dev Biol ; 9: 552549, 2021.
Article in English | MEDLINE | ID: mdl-33829010

ABSTRACT

The aggregation of α-synuclein is a hallmark of Parkinson's disease (PD) and a variety of related neurological disorders. A number of mutations in this protein, including A30P and A53T, are associated with familial forms of the disease. Patients carrying the A30P mutation typically exhibit a similar age of onset and symptoms as sporadic PD, while those carrying the A53T mutation generally have an earlier age of onset and an accelerated progression. We report two C. elegans models of PD (PDA30P and PDA53T), which express these mutational variants in the muscle cells, and probed their behavior relative to animals expressing the wild-type protein (PDWT). PDA30P worms showed a reduced speed of movement and an increased paralysis rate, control worms, but no change in the frequency of body bends. By contrast, in PDA53T worms both speed and frequency of body bends were significantly decreased, and paralysis rate was increased. α-Synuclein was also observed to be less well localized into aggregates in PDA30P worms compared to PDA53T and PDWT worms, and amyloid-like features were evident later in the life of the animals, despite comparable levels of expression of α-synuclein. Furthermore, squalamine, a natural product currently in clinical trials for treating symptomatic aspects of PD, was found to reduce significantly the aggregation of α-synuclein and its associated toxicity in PDA53T and PDWT worms, but had less marked effects in PDA30P. In addition, using an antibody that targets the N-terminal region of α-synuclein, we observed a suppression of toxicity in PDA30P, PDA53T and PDWT worms. These results illustrate the use of these two C. elegans models in fundamental and applied PD research.

6.
Cell Rep ; 34(2): 108608, 2021 01 12.
Article in English | MEDLINE | ID: mdl-33440146

ABSTRACT

Hereditary DNA repair defects affect tissues differently, suggesting that in vivo cells respond differently to DNA damage. Knowledge of the DNA damage response, however, is largely based on in vitro and cell culture studies, and it is currently unclear whether DNA repair changes depending on the cell type. Here, we use in vivo imaging of the nucleotide excision repair (NER) endonuclease ERCC-1/XPF-1 in C. elegans to demonstrate tissue-specific NER activity. In oocytes, XPF-1 functions as part of global genome NER (GG-NER) to ensure extremely rapid removal of DNA-helix-distorting lesions throughout the genome. In contrast, in post-mitotic neurons and muscles, XPF-1 participates in NER of transcribed genes only. Strikingly, muscle cells appear more resistant to the effects of DNA damage than neurons. These results suggest a tissue-specific organization of the DNA damage response and may help to better understand pleiotropic and tissue-specific consequences of accumulating DNA damage.


Subject(s)
Caenorhabditis elegans Proteins/metabolism , DNA Helicases/metabolism , DNA Repair , DNA-Binding Proteins/metabolism , Endonucleases/metabolism , Animals , Caenorhabditis elegans , Female , Muscles/metabolism , Muscles/radiation effects , Neurons/metabolism , Neurons/radiation effects , Oocytes/metabolism , Oocytes/radiation effects , Organ Specificity , Ultraviolet Rays
7.
Science ; 370(6519): 921, 2020 Nov 20.
Article in English | MEDLINE | ID: mdl-33214285
8.
EMBO J ; 38(8)2019 04 15.
Article in English | MEDLINE | ID: mdl-30914427

ABSTRACT

DNA-protein crosslinks (DPCs) are highly cytotoxic lesions that obstruct essential DNA transactions and whose resolution is critical for cell and organismal fitness. However, the mechanisms by which cells respond to and overcome DPCs remain incompletely understood. Recent studies unveiled a dedicated DPC repair pathway in higher eukaryotes involving the SprT-type metalloprotease SPRTN/DVC1, which proteolytically processes DPCs during DNA replication in a ubiquitin-regulated manner. Here, we show that chemically induced and defined enzymatic DPCs trigger potent chromatin SUMOylation responses targeting the crosslinked proteins and associated factors. Consequently, inhibiting SUMOylation compromises DPC clearance and cellular fitness. We demonstrate that ACRC/GCNA family SprT proteases interact with SUMO and establish important physiological roles of Caenorhabditis elegans GCNA-1 and SUMOylation in promoting germ cell and embryonic survival upon DPC formation. Our findings provide first global insights into signaling responses to DPCs and reveal an evolutionarily conserved function of SUMOylation in facilitating responses to these lesions in metazoans that may complement replication-coupled DPC resolution processes.


Subject(s)
Caenorhabditis elegans/growth & development , Chromatin/metabolism , Cross-Linking Reagents/metabolism , DNA-Binding Proteins/metabolism , DNA/metabolism , Nuclear Proteins/metabolism , Sumoylation , Animals , Caenorhabditis elegans/genetics , Caenorhabditis elegans/metabolism , Chromatin/genetics , DNA/genetics , DNA (Cytosine-5-)-Methyltransferase 1/genetics , DNA (Cytosine-5-)-Methyltransferase 1/metabolism , DNA Repair , DNA Replication , DNA-Binding Proteins/genetics , HeLa Cells , Humans , Kinetics , Nuclear Proteins/genetics , Proteolysis
9.
Nucleic Acids Res ; 46(18): 9563-9577, 2018 10 12.
Article in English | MEDLINE | ID: mdl-30165384

ABSTRACT

The structure-specific ERCC1-XPF endonuclease plays a key role in DNA damage excision by nucleotide excision repair (NER) and interstrand crosslink repair. Mutations in this complex can either cause xeroderma pigmentosum (XP) or XP combined with Cockayne syndrome (XPCS-complex) or Fanconi anemia. However, most patients carry compound heterozygous mutations, which confounds the dissection of the phenotypic consequences for each of the identified XPF alleles. Here, we analyzed the functional impact of individual pathogenic XPF alleles on NER. We show that XP-causing mutations diminish XPF recruitment to DNA damage and only mildly affect global genome NER. In contrast, an XPCS-complex-specific mutation causes persistent recruitment of XPF and the upstream core NER machinery to DNA damage and severely impairs both global genome and transcription-coupled NER. Remarkably, persistence of NER factors at DNA damage appears to be a common feature of XPCS-complex cells, suggesting that this could be a determining factor contributing to the development of additional developmental and/or neurodegenerative features in XP patients.


Subject(s)
Cockayne Syndrome/genetics , DNA-Binding Proteins/genetics , Endonucleases/genetics , Xeroderma Pigmentosum/genetics , Alleles , Cell Line , Cockayne Syndrome/pathology , DNA Damage/genetics , DNA Repair/genetics , DNA-Binding Proteins/chemistry , Endonucleases/chemistry , Fanconi Anemia/genetics , Fanconi Anemia/pathology , Genome, Human/genetics , Humans , Multiprotein Complexes/chemistry , Multiprotein Complexes/genetics , Mutation/genetics , Protein Multimerization/genetics
10.
Proc Natl Acad Sci U S A ; 109(37): 14912-7, 2012 Sep 11.
Article in English | MEDLINE | ID: mdl-22927396

ABSTRACT

Toxicity of aggregation-prone proteins is thought to play an important role in aging and age-related neurological diseases like Parkinson and Alzheimer's diseases. Here, we identify tryptophan 2,3-dioxygenase (tdo-2), the first enzyme in the kynurenine pathway of tryptophan degradation, as a metabolic regulator of age-related α-synuclein toxicity in a Caenorhabditis elegans model. Depletion of tdo-2 also suppresses toxicity of other heterologous aggregation-prone proteins, including amyloid-ß and polyglutamine proteins, and endogenous metastable proteins that are sensors of normal protein homeostasis. This finding suggests that tdo-2 functions as a general regulator of protein homeostasis. Analysis of metabolite levels in C. elegans strains with mutations in enzymes that act downstream of tdo-2 indicates that this suppression of toxicity is independent of downstream metabolites in the kynurenine pathway. Depletion of tdo-2 increases tryptophan levels, and feeding worms with extra L-tryptophan also suppresses toxicity, suggesting that tdo-2 regulates proteotoxicity through tryptophan. Depletion of tdo-2 extends lifespan in these worms. Together, these results implicate tdo-2 as a metabolic switch of age-related protein homeostasis and lifespan. With TDO and Indoleamine 2,3-dioxygenase as evolutionarily conserved human orthologs of TDO-2, intervening with tryptophan metabolism may offer avenues to reducing proteotoxicity in aging and age-related diseases.


Subject(s)
Aging/physiology , Homeostasis/physiology , Tryptophan Oxygenase/metabolism , Tryptophan/metabolism , alpha-Synuclein/toxicity , Aging/metabolism , Amyloid beta-Peptides/metabolism , Animals , Animals, Genetically Modified , Caenorhabditis elegans , Chromatography, Liquid , Computational Biology , DNA Primers/genetics , Fertility/genetics , Immunoblotting , Longevity/genetics , Peptides/metabolism , RNA Interference , Reverse Transcriptase Polymerase Chain Reaction , Tandem Mass Spectrometry , Tryptophan/chemistry , Tryptophan Oxygenase/antagonists & inhibitors
11.
PLoS Curr ; 3: RRN1255, 2011 Aug 12.
Article in English | MEDLINE | ID: mdl-21915392

ABSTRACT

Protein aggregation is a common hallmark of a number of age-related neurodegenerative diseases, including Alzheimer's, Parkinson's, and polyglutamine-expansion disorders such as Huntington's disease, but how aggregation-prone proteins lead to pathology is not known. Using a genome-wide RNAi screen in a C. elegans-model for polyglutamine aggregation, we previously identified 186 genes that suppress aggregation. Using an RNAi screen for human orthologs of these genes, we here present 26 human genes that suppress aggregation of mutant huntingtin in a human cell line. Among these are genes that have not been previously linked to mutant huntingtin aggregation. They include those encoding eukaryotic translation initiation, elongation and translation factors, and genes that have been previously associated with other neurodegenerative diseases, like the ATP-ase family gene 3-like 2 (AFG3L2) and ubiquitin-like modifier activating enzyme 1 (UBA1). Unravelling the role of these genes will broaden our understanding of the pathogenesis of Huntington's disease.

12.
Cell ; 142(4): 601-12, 2010 Aug 20.
Article in English | MEDLINE | ID: mdl-20723760

ABSTRACT

Fibrillar protein aggregates are the major pathological hallmark of several incurable, age-related, neurodegenerative disorders. These aggregates typically contain aggregation-prone pathogenic proteins, such as amyloid-beta in Alzheimer's disease and alpha-synuclein in Parkinson's disease. It is, however, poorly understood how these aggregates are formed during cellular aging. Here we identify an evolutionarily highly conserved modifier of aggregation, MOAG-4, as a positive regulator of aggregate formation in C. elegans models for polyglutamine diseases. Inactivation of MOAG-4 suppresses the formation of compact polyglutamine aggregation intermediates that are required for aggregate formation. The role of MOAG-4 in driving aggregation extends to amyloid-beta and alpha-synuclein and is evolutionarily conserved in its human orthologs SERF1A and SERF2. MOAG-4/SERF appears to act independently from HSF-1-induced molecular chaperones, proteasomal degradation, and autophagy. Our results suggest that MOAG-4/SERF regulates age-related proteotoxicity through a previously unexplored pathway, which will open up new avenues for research on age-related, neurodegenerative diseases.


Subject(s)
Caenorhabditis elegans Proteins/metabolism , Caenorhabditis elegans/metabolism , Cellular Senescence , Nerve Tissue Proteins/metabolism , Neurodegenerative Diseases/metabolism , Proteins/metabolism , Amyloid beta-Peptides/metabolism , Animals , Caenorhabditis elegans Proteins/chemistry , Cell Line , Cell Line, Tumor , Humans , Intracellular Signaling Peptides and Proteins , Mice , Nerve Tissue Proteins/chemistry , Peptides/metabolism , Proteins/chemistry , alpha-Synuclein/metabolism
13.
PLoS Genet ; 4(3): e1000027, 2008 Mar 21.
Article in English | MEDLINE | ID: mdl-18369446

ABSTRACT

Inclusions in the brain containing alpha-synuclein are the pathological hallmark of Parkinson's disease, but how these inclusions are formed and how this links to disease is poorly understood. We have developed a C. elegans model that makes it possible to monitor, in living animals, the formation of alpha-synuclein inclusions. In worms of old age, inclusions contain aggregated alpha- synuclein, resembling a critical pathological feature. We used genome-wide RNA interference to identify processes involved in inclusion formation, and identified 80 genes that, when knocked down, resulted in a premature increase in the number of inclusions. Quality control and vesicle-trafficking genes expressed in the ER/Golgi complex and vesicular compartments were overrepresented, indicating a specific role for these processes in alpha-synuclein inclusion formation. Suppressors include aging-associated genes, such as sir-2.1/SIRT1 and lagr-1/LASS2. Altogether, our data suggest a link between alpha-synuclein inclusion formation and cellular aging, likely through an endomembrane-related mechanism. The processes and genes identified here present a framework for further study of the disease mechanism and provide candidate susceptibility genes and drug targets for Parkinson's disease and other alpha-synuclein related disorders.


Subject(s)
Aging/genetics , Aging/metabolism , Caenorhabditis elegans/genetics , Caenorhabditis elegans/metabolism , Inclusion Bodies/metabolism , alpha-Synuclein/genetics , alpha-Synuclein/metabolism , Animals , Animals, Genetically Modified , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Base Sequence , Brain/metabolism , DNA Primers/genetics , Fluorescence Recovery After Photobleaching , G-Protein-Coupled Receptor Kinases/antagonists & inhibitors , G-Protein-Coupled Receptor Kinases/genetics , G-Protein-Coupled Receptor Kinases/metabolism , Gene Deletion , Genes, Helminth , Humans , Luminescent Proteins/genetics , Luminescent Proteins/metabolism , Models, Genetic , Parkinson Disease/etiology , Parkinson Disease/genetics , Parkinson Disease/metabolism , RNA Interference , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , alpha-Synuclein/antagonists & inhibitors
14.
Nat Struct Mol Biol ; 14(10): 927-33, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17891148

ABSTRACT

In C. elegans, DCR-1 is required for the maturation of both short interfering RNAs (siRNAs) and microRNAs (miRNAs), which are subsequently loaded into different Argonaute proteins to mediate silencing via distinct mechanisms. We used in vivo analyses to show that precursors of small RNAs contain structural features that direct the small RNAs into the RNA interference (RNAi) pathway or the miRNA-processing pathway. Nucleotide changes in the pre-let-7 miRNA precursor that make its stem fully complementary cause the resulting small RNA to be recognized as siRNA and induce binding to RDE-1, which leads to RNAi. Mismatches of 1 to 3 nucleotides at various positions in the stem of the precursor restore direction into the miRNA pathway, as the largest portion of such small RNA variants is associated with ALG-1. The Argonaute proteins to which the small RNAs are bound determine the silencing mode, and no functional overlap between RDE-1 and ALG-1 was detected.


Subject(s)
Caenorhabditis elegans Proteins/chemistry , Caenorhabditis elegans Proteins/metabolism , Caenorhabditis elegans , Nucleic Acid Conformation , RNA Interference , RNA Precursors/chemistry , RNA Precursors/metabolism , Animals , Animals, Genetically Modified , Base Sequence , Caenorhabditis elegans/genetics , Caenorhabditis elegans/metabolism , Caenorhabditis elegans Proteins/genetics , Endoribonucleases/genetics , Endoribonucleases/metabolism , Gene Silencing , MicroRNAs/genetics , MicroRNAs/metabolism , Molecular Sequence Data , RNA Precursors/genetics , RNA, Small Interfering/genetics , RNA, Small Interfering/metabolism , Ribonuclease III
15.
Science ; 315(5809): 244-7, 2007 01 12.
Article in English | MEDLINE | ID: mdl-17158288

ABSTRACT

In Caenorhabditis elegans, an effective RNA interference (RNAi) response requires the production of secondary short interfering RNAs (siRNAs) by RNA-directed RNA polymerases (RdRPs). We cloned secondary siRNAs from transgenic C. elegans lines expressing a single 22-nucleotide primary siRNA. Several secondary siRNAs start a few nucleotides downstream of the primary siRNA, indicating that non-RISC (RNA-induced silencing complex)-cleaved mRNAs are substrates for secondary siRNA production. In lines expressing primary siRNAs with single-nucleotide mismatches, secondary siRNAs do not carry the mismatch but contain the nucleotide complementary to the mRNA. We infer that RdRPs perform unprimed RNA synthesis. Secondary siRNAs are only of antisense polarity, carry 5' di- or triphosphates, and are only in the minority associated with RDE-1, the RNAi-specific Argonaute protein. Therefore, secondary siRNAs represent a distinct class of small RNAs. Their biogenesis depends on RdRPs, and we propose that each secondary siRNA is an individual RdRP product.


Subject(s)
Caenorhabditis elegans/genetics , RNA Interference , RNA, Antisense/biosynthesis , RNA, Helminth/biosynthesis , RNA, Small Interfering/biosynthesis , Animals , Animals, Genetically Modified , Base Pairing , Caenorhabditis elegans/metabolism , Caenorhabditis elegans Proteins/metabolism , Cloning, Molecular , Phosphates/analysis , RNA, Antisense/chemistry , RNA, Antisense/metabolism , RNA, Complementary/biosynthesis , RNA, Helminth/genetics , RNA, Helminth/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , RNA, Small Interfering/chemistry , RNA, Small Interfering/metabolism , RNA-Dependent RNA Polymerase/metabolism , Ribonuclease III/metabolism
16.
Curr Biol ; 13(15): 1311-6, 2003 Aug 05.
Article in English | MEDLINE | ID: mdl-12906791

ABSTRACT

Transposon jumps are a major cause of genome instability. In the C. elegans strain Bristol N2, transposons are active in somatic cells, but they are silenced in the germline, presumably to protect the germline from mutations. Interestingly, the transposon-silencing mechanism shares factors with the RNAi machinery. To better understand the mechanism of transposon silencing, we performed a genome-wide RNAi screen for genes that, when silenced, cause transposition of Tc1 in the C. elegans germline. We identified 27 such genes, among which are mut-16, a mutator that was previously found but not identified at the molecular level, ppw-2, a member of the argonaute family, and several factors that indicate a role for chromatin structure in the regulation of transposition. Some of the newly identified genes are also required for cosuppression and therefore represent the shared components of the two pathways. Since most of the newly identified genes have clear homologs in other species, and since transposons are found from protozoa to human, it seems likely that they also protect other genomes against transposon activity in the germline.


Subject(s)
Caenorhabditis elegans/genetics , DNA Transposable Elements/genetics , Genome , Genomic Instability/genetics , RNA Interference , Suppression, Genetic/genetics , Animals , Chromosome Mapping , Gene Expression Profiling
17.
Genes Dev ; 17(4): 443-8, 2003 Feb 15.
Article in English | MEDLINE | ID: mdl-12600937

ABSTRACT

An RNA interference (RNAi)-based genome-wide screen was performed to detect genes that contribute to genome stability in somatic cells of Caenorhabditis elegans. We identified 61 such genes; these also affect spontaneous mutagenesis in the germ line. Their sequence suggests a role in DNA repair and/or replication, in chromatin remodeling, or in cell cycle control; there are also many novel genes that are highly conserved from yeast to human. Because known mutator genes are causally involved in many hereditary and sporadic human cancers, it is likely that some of these new mutators are equally relevant in cancer etiology.


Subject(s)
Caenorhabditis elegans/genetics , Genes, Helminth , Membrane Proteins , Mutation , RNA Interference , Animals , Animals, Genetically Modified , Caenorhabditis elegans Proteins/classification , Caenorhabditis elegans Proteins/genetics , Cell Cycle/genetics , Chromatin/genetics , Chromatin/metabolism , DNA Repair/genetics , DNA Replication/genetics , Genome , Helminth Proteins/genetics , Muscle Proteins/genetics , RNA, Helminth , Sequence Homology, Nucleic Acid
18.
Curr Biol ; 12(17): 1535-40, 2002 Sep 03.
Article in English | MEDLINE | ID: mdl-12225671

ABSTRACT

One of the remarkable aspects about RNA interference (RNAi) in Caenorhabditis elegans is that the trigger molecules, dsRNA, can be administered via the animal's food. We assayed whether this feature is a universal property of the species by testing numerous strains that have been isolated from different parts of the globe. We found that one isolate from Hawaii had a defect in RNAi that was specific to the germline and was a result of multiple mutations in a PAZ/PIWI domain-containing protein, which we named PPW-1. Deleting ppw-1 in the canonical C. elegans strain Bristol N2 makes it resistant to feeding of dsRNA directed against germline-expressed genes. PPW-1 belongs to the Argonaute family of proteins, which act in posttranscriptional gene silencing and development, and is homologous to the RNAi gene rde-1. Our data indicate that at least two members of this family are required for complete and effective RNAi in C. elegans.


Subject(s)
Caenorhabditis elegans Proteins/genetics , Caenorhabditis elegans/genetics , Gene Silencing , RNA Interference , RNA, Small Interfering/genetics , Amino Acid Sequence , Animals , Animals, Genetically Modified , Caenorhabditis elegans Proteins/physiology , Eating , England , Genes, Helminth , Hawaii , Molecular Sequence Data , Multigene Family , Phenotype , Protein Structure, Tertiary , RNA, Double-Stranded/administration & dosage , Species Specificity
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