A strand invasion 3' polymerization intermediate of mammalian homologous recombination.

Abstract:

:Initial events in double-strand break repair by homologous recombination in vivo involve homology searching, 3' strand invasion, and new DNA synthesis. While studies in yeast have contributed much to our knowledge of these processes, in comparison, little is known of the early events in the integrated mammalian system. In this study, a sensitive PCR procedure was developed to detect the new DNA synthesis that accompanies mammalian homologous recombination. The test system exploits a well-characterized gene targeting assay in which the transfected vector bears a gap in the region of homology to the single-copy chromosomal immunoglobulin mu heavy chain gene in mouse hybridoma cells. New DNA synthesis primed by invading 3' vector ends copies chromosomal mu-gene template sequences excluded by the vector-borne double-stranded gap. Following electroporation, specific 3' extension products from each vector end are detected with rapid kinetics: they appear after 0.5 hr, peak at 3-6 hr, and then decline, likely as a result of the combined effects of susceptibility to degradation and cell division. New DNA synthesis from each vector 3' end extends at least approximately 1000 nucleotides into the gapped region, but the efficiency declines markedly within the first approximately 200 nucleotides. Over this short distance, an average frequency of 3' extension for the two invading vector ends is approximately 0.007 events/vector backbone. DNA sequencing reveals precise copying of the cognate chromosomal mu-gene template. In unsynchronized cells, 3' extension is sensitive to aphidicolin supporting involvement of a replicative polymerase. Analysis suggests that the vast majority of 3' extensions reside on linear plasmid molecules.

journal_name

Genetics

journal_title

Genetics

authors

Si W,Mundia MM,Magwood AC,Mark AL,McCulloch RD,Baker MD

doi

10.1534/genetics.110.115196

subject

Has Abstract

pub_date

2010-06-01 00:00:00

pages

443-57

issue

2

eissn

0016-6731

issn

1943-2631

pii

genetics.110.115196

journal_volume

185

pub_type

杂志文章

相关文献

GENETICS文献大全
  • Patterns of selection against transposons inferred from the distribution of Tc1, Tc3 and Tc5 insertions in the mut-7 line of the nematode Caenorhabditis elegans.

    abstract::To identify the factors (selective or mutational) that affect the distribution of transposable elements (TEs) within a genome, it is necessary to compare the pattern of newly arising element insertions to the pattern of element insertions that have been fixed in a population. To do this, we analyzed the distribution o...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Rizzon C,Martin E,Marais G,Duret L,Ségalat L,Biémont C

    更新日期:2003-11-01 00:00:00

  • Induction of mitotic crossing over in Saccharomyces cerevisiae by breakdown products of dimethylnitrosamine, diethylnitrosamine, 1-naphthylamine and 2-naphthylamine formed by an in vitro hydroxylation system.

    abstract::Dimethylnitrosamine and diethylnitrosamine, two potent carcinogens, are nonmutagenic when tested directly in microorganisms. Likewise 1-naphthylamine and 2-naphthylamine are also nonmutagenic but the N-hydroxy derivatives are mutagenic in microorganisms. Apparently these compounds require metabolism to breakdown produ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Mayer VW

    更新日期:1973-07-01 00:00:00

  • Two mutations in a maize bronze-1 allele caused by transposable elements of the Ac-Ds family alter the quantity and quality of the gene product.

    abstract::The Dissociation (Ds) mutant, Bz-wm, of the maize bronze-1 (bz) locus conditions a leaky phenotype. Plants carrying this mutant allele synthesize a low amount of an altered Bz gene product, which leads to reduced anthocyanin pigmentation in the seed. The molecular analysis reported here shows that the Bz-wm mutant has...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Schiefelbein JW,Furtek DB,Dooner HK,Nelson OE Jr

    更新日期:1988-11-01 00:00:00

  • Nuclear mutation increases streptomycin and spectinomycin sensitivity in Chlamydomonas.

    abstract::A spontaneously arising nuclear mutation, ss-1, has been identified in Chlamydomonas reinhardtii that decreases both streptomycin and spectinomycin resistance levels about 10-fold after its introduction into all wild-type, streptomycin-resistant and spectinomycin-resistant strains examined. The mutations for resistanc...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Lee RW,Sapp JA

    更新日期:1978-04-01 00:00:00

  • Evolution of mouse T-box genes by tandem duplication and cluster dispersion.

    abstract::The T-box genes comprise an ancient family of putative transcription factors conserved across species as divergent as Mus musculus and Caenorhabditis elegans. All T-box gene products are characterized by a novel 174-186-amino acid DNA binding domain called the T-box that was first discovered in the polypeptide product...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Agulnik SI,Garvey N,Hancock S,Ruvinsky I,Chapman DL,Agulnik I,Bollag R,Papaioannou V,Silver LM

    更新日期:1996-09-01 00:00:00

  • Drug-sensitive DNA polymerase δ reveals a role for mismatch repair in checkpoint activation in yeast.

    abstract::We have used a novel method to activate the DNA damage S-phase checkpoint response in Saccharomyces cerevisiae to slow lagging-strand DNA replication by exposing cells expressing a drug-sensitive DNA polymerase δ (L612M-DNA pol δ) to the inhibitory drug phosphonoacetic acid (PAA). PAA-treated pol3-L612M cells arrest a...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.111.131938

    authors: Reha-Krantz LJ,Siddique MS,Murphy K,Tam A,O'Carroll M,Lou S,Schultz A,Boone C

    更新日期:2011-12-01 00:00:00

  • Phenotypes of mutations in the 5'-UTR of a limiting transcription factor in Aspergillus nidulans can be accounted for by translational inhibition and leaky scanning.

    abstract::The uaY gene encodes the transcriptional activator of purine catabolism genes in Aspergillus nidulans. uaY12 results in strongly defective growth on purines as nitrogen sources and in strongly diminished transcription of UaY-regulated genes. This mutation introduces an ATG codon 64 bp upstream of the uaY ATG, generati...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.108.099515

    authors: Oestreicher N,Scazzocchio C

    更新日期:2009-04-01 00:00:00

  • Repair of a mismatch is influenced by the base composition of the surrounding nucleotide sequence.

    abstract::Heteroduplexes with single base pair mismatches of known sequence were prepared by annealing separated strands of bacteriophage lambda DNA and used to transfect Escherichia coli. A series of transition (G:T and A:C) and transversion (G:A and C:T) mismatches located throughout most of the bacteriophage lambda cI gene h...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Jones M,Wagner R,Radman M

    更新日期:1987-04-01 00:00:00

  • Recombination can evolve in large finite populations given selection on sufficient loci.

    abstract::It is well known that an allele causing increased recombination is expected to proliferate as a result of genetic drift in a finite population undergoing selection, without requiring other mechanisms. This is supported by recent simulations apparently demonstrating that, in small populations, drift is more important t...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Iles MM,Walters K,Cannings C

    更新日期:2003-12-01 00:00:00

  • Homologous recombination between autonomously replicating plasmids in mammalian cells.

    abstract::The ability of autonomously replicating plasmids to recombine in mammalian cells was investigated. Two deletion plasmids of the eukaryotic-prokaryotic shuttle vector pSV2neo were cotransfected into transformed monkey COS cells. Examination of the low molecular weight DNA isolated after 48 hr of incubation revealed tha...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Ayares D,Spencer J,Schwartz F,Morse B,Kucherlapati R

    更新日期:1985-10-01 00:00:00

  • The promotion of gonadal cell divisions by the Caenorhabditis elegans TRPM cation channel GON-2 is antagonized by GEM-4 copine.

    abstract::The initiation of postembryonic cell divisions by the gonadal precursors of C. elegans requires the activity of gon-2. gon-2 encodes a predicted cation channel (GON-2) of the TRPM subfamily of TRP proteins and is likely to mediate the influx of Ca(2+) and/or Mg(2+). We report here that mutations in gem-4 (gon-2 extrag...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Church DL,Lambie EJ

    更新日期:2003-10-01 00:00:00

  • Genome analysis of Chlamydomonas reinhardtii reveals the existence of multiple, compartmentalized iron-sulfur protein assembly machineries of different evolutionary origins.

    abstract::The unicellular green alga Chlamydomonas reinhardtii is used extensively as a model to study eukaryotic photosynthesis, flagellar functions, and more recently the production of hydrogen as biofuel. Two of these processes, photosynthesis and hydrogen production, are highly dependent on iron-sulfur (Fe-S) enzymes. To un...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.107.086033

    authors: Godman J,Balk J

    更新日期:2008-05-01 00:00:00

  • Intragenic Suppression at the b2 Locus in ASCOBOLUS IMMERSUS. II. Characteristics of the Mutations in Groups A and E.

    abstract::The present report is a study of 60 intragenic suppressors located in the A or E group of the b2 spore-color locus of Ascobolus immersus. The frameshift nature of the suppressors was shown by 19 combinations of plus and minus suppressor mutations. The location of the mutation sites on the genetic map of group A was de...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Leblon G

    更新日期:1979-08-01 00:00:00

  • Genetic analysis of X-chromosome dosage compensation in Caenorhabditis elegans.

    abstract::We have shown that the phenotypes resulting from hypomorphic mutations (causing reduction but not complete loss of function) in two X-linked genes can be used as a genetic assay for X-chromosome dosage compensation in Caenorhabditis elegans between males (XO) and hermaphrodites (XX). In addition we show that recessive...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Meneely PM,Wood WB

    更新日期:1987-09-01 00:00:00

  • A modifier gene alleviates hypothyroidism-induced hearing impairment in Pou1f1dw dwarf mice.

    abstract::Thyroid hormone has pleiotropic effects on cochlear development, and genomic variation influences the severity of associated hearing deficits. DW/J-Pou1f1dw/dw mutant mice lack pituitary thyrotropin, which causes severe thyroid hormone deficiency and profound hearing impairment. To assess the genetic complexity of pro...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.111.130633

    authors: Fang Q,Longo-Guess C,Gagnon LH,Mortensen AH,Dolan DF,Camper SA,Johnson KR

    更新日期:2011-10-01 00:00:00

  • Regulation of epithelial stem cell replacement and follicle formation in the Drosophila ovary.

    abstract::Though much has been learned about the process of ovarian follicle maturation through studies of oogenesis in both vertebrate and invertebrate systems, less is known about how follicles form initially. In Drosophila, two somatic follicle stem cells (FSCs) in each ovariole give rise to all polar cells, stalk cells, and...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.109.109538

    authors: Nystul T,Spradling A

    更新日期:2010-02-01 00:00:00

  • A pseudohitchhiking model of X vs. autosomal diversity.

    abstract::We study levels of X-linked vs. autosomal diversity using a model developed to analyze the hitchhiking effect. Repeated bouts of hitchhiking are thought to lower X-linked diversity for two reasons: first, because sojourn times of beneficial mutations are shorter on the X, and second, because adaptive substitutions may...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.104.030999

    authors: Betancourt AJ,Kim Y,Orr HA

    更新日期:2004-12-01 00:00:00

  • Action of repeat-induced point mutation on both strands of a duplex and on tandem duplications of various sizes in Neurospora.

    abstract::In Neurospora crassa, DNA sequence duplications are detected and altered efficiently during the sexual cycle by a process known as RIP (repeat-induced point mutation). Affected sequences are subjected to multiple GC-to-AT mutations. To explore the pattern in which base changes are laid down by RIP we examined two sets...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Watters MK,Randall TA,Margolin BS,Selker EU,Stadler DR

    更新日期:1999-10-01 00:00:00

  • Partial selfing and linkage: the effect of a heterotic locus on a neutral locus.

    abstract::Equilibria are determined for the two-locus model in a partially selfing population when one locus is neutral and the other locus is heterotic. At an equilibrium point, the frequency of heterozygotes at the neutral locus is greater than that expected from one-locus theory, even if the heterotic locus is on a different...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Strobeck C

    更新日期:1979-05-01 00:00:00

  • Fold recognition of the human immunodeficiency virus type 1 V3 loop and flexibility of its crown structure during the course of adaptation to a host.

    abstract::The third hypervariable (V3) region of the HIV-1 gp120 protein is responsible for many aspects of viral infectivity. The tertiary structure of the V3 loop seems to influence the coreceptor usage of the virus, which is an important determinant of HIV pathogenesis. Hence, the information about preferred conformations of...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.051508

    authors: Watabe T,Kishino H,Okuhara Y,Kitazoe Y

    更新日期:2006-03-01 00:00:00

  • Prediction of rates of inbreeding in populations selected on best linear unbiased prediction of breeding value

    abstract::Predictions for the rate of inbreeding (DeltaF) in populations with discrete generations undergoing selection on best linear unbiased prediction (BLUP) of breeding value were developed. Predictions were based on the concept of long-term genetic contributions using a recently established relationship between expected c...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Bijma P,Woolliams JA

    更新日期:2000-09-01 00:00:00

  • Cloning of a mutable bz2 allele of maize by transposon tagging and differential hybridization.

    abstract::Sequences of Bronze2 (Bz2), a maize gene which is required for the synthesis of the purple pigment anthocyanin, have been cloned by combining the techniques of transposon tagging and differential hybridization. First, a mutable bz2 allele (bz2-mu1) was recovered from a Mutator line. The mutation was assumed to result ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: McLaughlin M,Walbot V

    更新日期:1987-12-01 00:00:00

  • Two alternative transcripts coding for alcohol dehydrogenase accumulate with different developmental specificities in different species of picture-winged Drosophila.

    abstract::Two alternate transcripts of the single copy Alcohol dehydrogenase (Adh) gene accumulate with developmental specificity in all of 12 species of Hawaiian picture-winged Drosophila which have been examined. Relative to the paradigm species D. affinidisjuncta, the Adh transcript normally restricted to larvae is found to ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Rowan RG,Dickinson WJ

    更新日期:1986-10-01 00:00:00

  • Molecular proxies for climate maladaptation in a long-lived tree (Pinus pinaster Aiton, Pinaceae).

    abstract::Understanding adaptive genetic responses to climate change is a main challenge for preserving biological diversity. Successful predictive models for climate-driven range shifts of species depend on the integration of information on adaptation, including that derived from genomic studies. Long-lived forest trees can ex...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.114.173252

    authors: Jaramillo-Correa JP,Rodríguez-Quilón I,Grivet D,Lepoittevin C,Sebastiani F,Heuertz M,Garnier-Géré PH,Alía R,Plomion C,Vendramin GG,González-Martínez SC

    更新日期:2015-03-01 00:00:00

  • Geographical distribution of twelve transferrin alleles in black rats of Asia and Oceania.

    abstract::About 450 black rats (Rattus rattus) were collected from 25 localities in Asia and Oceania. Their serum transferrins were analyzed by a newly developed thin layer acrylamide gel electrophoresis accompanied with acrinol pretreatment, exhibiting 12 transferrin bands. Generally, Asian type rats (2N=42) had fast-moving tr...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Moriwaki K,Kato H,ImalH,Tsuchiya K,Yosida T

    更新日期:1975-02-01 00:00:00

  • Probabilistic prediction of unknown metabolic and signal-transduction networks.

    abstract::Regulatory networks provide control over complex cell behavior in all kingdoms of life. Here we describe a statistical model, based on representing proteins as collections of domains or motifs, which predicts unknown molecular interactions within these biological networks. Using known protein-protein interactions of S...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Gomez SM,Lo SH,Rzhetsky A

    更新日期:2001-11-01 00:00:00

  • Quantitative trait loci mapping and the genetic basis of heterosis in maize and rice.

    abstract::Despite its importance to agriculture, the genetic basis of heterosis is still not well understood. The main competing hypotheses include dominance, overdominance, and epistasis. NC design III is an experimental design that has been used for estimating the average degree of dominance of quantitative trait loci (QTL) a...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.107.082867

    authors: Garcia AA,Wang S,Melchinger AE,Zeng ZB

    更新日期:2008-11-01 00:00:00

  • On the structure of gene control regions.

    abstract::A model emphasizing the possible genetic role of tandem duplications of reverse repeats has been developed as an extension of Crick's (1971) general model for the chromosomes of higher organisms. Although developed initially (1) to explain why random differences in the control regions of individual gene loci might con...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Wallace B,Kass TL

    更新日期:1974-07-01 00:00:00

  • Genotyping Polyploids from Messy Sequencing Data.

    abstract::Detecting and quantifying the differences in individual genomes (i.e., genotyping), plays a fundamental role in most modern bioinformatics pipelines. Many scientists now use reduced representation next-generation sequencing (NGS) approaches for genotyping. Genotyping diploid individuals using NGS is a well-studied fie...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.118.301468

    authors: Gerard D,Ferrão LFV,Garcia AAF,Stephens M

    更新日期:2018-11-01 00:00:00

  • Immunogenetic polymorphism of lipoproteins in swine: genetic, immunological and physiochemical characterization of the two allotypes Lpr1 and Lpr2.

    abstract::Results of immunogenetic, immunochemical and physicochemical investigations on two serum allotypes of swine are reported. The allotypes, designated Lpr1 and Lpr2, have been identified by specific alloprecipitins in agar gel. Genetic studies indicate that the allotypes are specified by two codominant autosomal allelic ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Rapacz J,Hasler-Rapacz J,Kuo WH

    更新日期:1986-08-01 00:00:00