ArticleNucleic acids research2002
Improved detection of small deletions in complex pools of DNA.
Article in Nucleic acids research, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.
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Who cites it
32 citing papers in PubMed.
- RAG1/2 induces genomic insertions by mobilizing DNA into RAG1/2-independent breaks.The Journal of experimental medicine · 2017Article
- Genomic Scars Generated by Polymerase Theta Reveal the Versatile Mechanism of Alternative End-Joining.PLoS genetics · 2016Article
- The application of CRISPR-Cas9 genome editing in Caenorhabditis elegans.Journal of genetics and genomics = Yi chuan xue bao · 2015Review
- Dual sgRNA-directed gene knockout using CRISPR/Cas9 technology in Caenorhabditis elegans.Scientific reports · 2014Article
- UNC-6 (netrin) stabilizes oscillatory clustering of the UNC-40 (DCC) receptor to orient polarity.The Journal of cell biology · 2014Article
- Forward and reverse mutagenesis in C. elegans.WormBook : the online review of C. elegans biology · 2014Review
- Article
- large-scale screening for targeted knockouts in the Caenorhabditis elegans genome.G3 (Bethesda, Md.) · 2012Article
- A regulatory module controlling pharyngeal development and function in Caenorhabditis elegans.Genetics · 2012Article
- Context-dependent function of a conserved translational regulatory module.Development (Cambridge, England) · 2012Article
- The thioredoxin TRX-1 modulates the function of the insulin-like neuropeptide DAF-28 during dauer formation in Caenorhabditis elegans.PloS one · 2011Article
- New tools for investigating the comparative biology of Caenorhabditis briggsae and C. elegans.Genetics · 2010Article
- Characterization of the astacin family of metalloproteases in C. elegans.BMC developmental biology · 2010Article
- Deletion-based reverse genetics in Medicago truncatula.Plant physiology · 2009Article
- An ER-resident membrane protein complex regulates nicotinic acetylcholine receptor subunit composition at the synapse.The EMBO journal · 2009Article
- Isolation of deletion alleles by G4 DNA-induced mutagenesis.Nature methods · 2009Article
- IgCAMs redundantly control axon navigation in Caenorhabditis elegans.Neural development · 2009Article
- The FLYWCH transcription factors FLH-1, FLH-2, and FLH-3 repress embryonic expression of microRNA genes in C. elegans.Genes & development · 2008Article
- A comparative metabolomic study of NHR-49 in Caenorhabditis elegans and PPAR-alpha in the mouse.FEBS letters · 2008Article
- Article
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8 authors.
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Abstract
About 40% of the genes in the nematode Caenorhabditis elegans have homologs in humans. Based on the history of this model system, it is clear that the application of genetic methods to the study of this set of genes would provide important clues to their function in humans. To facilitate such genetic studies, we are engaged in a project to derive deletion alleles in every gene in this set. Our standard methods make use of nested PCR to hunt for animals in mutagenized populations that carry deletions at a given locus. The deletion bearing animals exist initially in mixed populations where the majority of the animals are wild type at the target. Therefore, the production of the PCR fragment representing the deletion allele competes with the production of the wild type fragment. The size of the deletion fragment relative to wild type determines whether it can compete to a level where it can be detected above the background. Using our standard conditions, we have found that when the deletion is <600 bp, the deletion fragment does not compete effectively with the production of the wild type fragment in PCR. Therefore, although our standard methods work well to detect mutants with deletions >600 bp, they do not work well to detect mutants with smaller deletions. Here we report a new strategy to detect small deletion alleles in complex DNA pools. Our new strategy is a modification of our standard PCR based screens. In the first round of the nested PCR, we include a third PCR primer between the two external primers. The presence of this third primer leads to the production of three fragments from wild type DNA. We configure the system so that two of these three fragments cannot serve as a template in the second round of the nested PCR. The addition of this third primer, therefore, handicaps the amplification from wild type template. On the other hand, the amplification of mutant fragments where the binding site for the third primer is deleted is unabated. Overall, we see at least a 500-fold increase in the sensitivity for small deletion fragments using our new method. Using this new method, we report the recovery of new deletion alleles within 12 C.elegans genes.
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