Genetic requirements for spontaneous and transcription-stimulated mitotic recombination in Saccharomyces cerevisiae.

Abstract:

:The genetic requirements for spontaneous and transcription-stimulated mitotic recombination were determined using a recombination system that employs heterochromosomal lys2 substrates that can recombine only by crossover or only by gene conversion. The substrates were fused either to a constitutive low-level promoter (pLYS) or to a highly inducible promoter (pGAL). In the case of the "conversion-only" substrates the use of heterologous promoters allowed either the donor or the recipient allele to be highly transcribed. Transcription of the donor allele stimulated gene conversions in rad50, rad51, rad54, and rad59 mutants, but not in rad52, rad55, and rad57 mutants. In contrast, transcription of the recipient allele stimulated gene conversions in rad50, rad51, rad54, rad55, rad57, and rad59 mutants, but not in rad52 mutants. Finally, transcription stimulated crossovers in rad50, rad54, and rad59 mutants, but not in rad51, rad52, rad55, and rad57 mutants. These data are considered in relation to previously proposed molecular mechanisms of transcription-stimulated recombination and in relation to the roles of the recombination proteins.

journal_name

Genetics

journal_title

Genetics

authors

Freedman JA,Jinks-Robertson S

keywords:

subject

Has Abstract

pub_date

2002-09-01 00:00:00

pages

15-27

issue

1

eissn

0016-6731

issn

1943-2631

journal_volume

162

pub_type

杂志文章

相关文献

GENETICS文献大全
  • Genetic modifiers of Drosophila palmitoyl-protein thioesterase 1-induced degeneration.

    abstract::Infantile neuronal ceroid lipofuscinosis (INCL) is a pediatric neurodegenerative disease caused by mutations in the human CLN1 gene. CLN1 encodes palmitoyl-protein thioesterase 1 (PPT1), suggesting an important role for the regulation of palmitoylation in normal neuronal function. To further elucidate Ppt1 function, w...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.106.067983

    authors: Buff H,Smith AC,Korey CA

    更新日期:2007-05-01 00:00:00

  • The maize NCS2 abnormal growth mutant has a chimeric nad4-nad7 mitochondrial gene and is associated with reduced complex I function.

    abstract::The molecular basis of the maternally inherited, heteroplasmic NCS2 mutant of maize was investigated. Analysis of the NCS2 mtDNA showed that it closely resembles the progenitor cmsT mitochondrial genome, except that the mutant genome contains a fused nad4-nad7 gene and is deleted for the small fourth exon of nad4. The...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Marienfeld JR,Newton KJ

    更新日期:1994-11-01 00:00:00

  • The isolation and characterization of Saccharomyces cerevisiae mutants that constitutively express purine biosynthetic genes.

    abstract::In response to an external source of adenine, yeast cells repress the expression of purine biosynthesis pathway genes. To identify necessary components of this signalling mechanism, we have isolated mutants that are constitutively active for expression. These mutants were named bra (for bypass of repression by adenine...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Guetsova ML,Lecoq K,Daignan-Fornier B

    更新日期:1997-10-01 00:00:00

  • Focused genetic recombination of bacteriophage t4 initiated by double-strand breaks.

    abstract::A model system for studying double-strand-break (DSB)-induced genetic recombination in vivo based on the ets1 segCDelta strain of bacteriophage T4 was developed. The ets1, a 66-bp DNA fragment of phage T2L containing the cleavage site for the T4 SegC site-specific endonuclease, was inserted into the proximal part of t...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Shcherbakov V,Granovsky I,Plugina L,Shcherbakova T,Sizova S,Pyatkov K,Shlyapnikov M,Shubina O

    更新日期:2002-10-01 00:00:00

  • Mapping quantitative trait loci for longitudinal traits in line crosses.

    abstract::Quantitative traits whose phenotypic values change over time are called longitudinal traits. Genetic analyses of longitudinal traits can be conducted using any of the following approaches: (1) treating the phenotypic values at different time points as repeated measurements of the same trait and analyzing the trait und...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.054775

    authors: Yang R,Tian Q,Xu S

    更新日期:2006-08-01 00:00:00

  • A sex chromosomal restriction-fragment-length marker linked to melanoma-determining Tu loci in Xiphophorus.

    abstract::In Xiphophorus, the causative genetic information for melanoma formation has been assigned by classical genetics to chromosomal loci, which are located on the sex chromosomes. In our attempts to molecularly clone these melanoma-determining loci, named Tu, we have looked for restriction-fragment-length markers (RFLMs) ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Schartl M

    更新日期:1988-07-01 00:00:00

  • Genetic effects of acute spermatogonial X-irradiation of the laboratory rat.

    abstract::The genetic effects of one generation of spermatogonial X-irradiation in rats, by a single dose of 600r in one experiment and by a fractionated dose of 450r in another, were measured in three generations of their descendants. Estimates of dominant lethal mutation rates--(2 to 3) X 10-4/gamete/r--from litter size diffe...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Chambers JR,Chapman AB

    更新日期:1977-02-01 00:00:00

  • Linkage relationships reflecting ancestral tetraploidy in salmonid fish.

    abstract::Fifteen classical linkage groups were identified in two salmonid species (Salmo trutta and Salmo gairdneri) and three fertile, interspecific hybrids (S. gairdneri X Salmo clarki, Salvelinus fontinalis X Salvelinus namaycush and S. fontinalis X Salvelinus alpinus) by backcrossing multiply heterozygous individuals. Thes...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Johnson KR,Wright JE Jr,May B

    更新日期:1987-08-01 00:00:00

  • On the identification of the rosy locus DNA in Drosophila melanogaster: intragenic recombination mapping of mutations associated with insertions and deletions.

    abstract::DNA extracts of several rosy-mutation-bearing strains were associated with large insertions and deletions in a defined region of the molecular map believed to include the rosy locus DNA. Large-scale, intragenic mapping experiments were carried out that localized these mutations within the boundaries of the previously ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Clark SH,McCarron M,Love C,Chovnick A

    更新日期:1986-04-01 00:00:00

  • Assembly of the mitochondrial membrane system: nuclear suppression of a cytochrome b mutation in yeast mitochondrial DNA.

    abstract::In a previous study, a mitochondrial mutant expressing a specific enzymatic deficiency in co-enzyme QH2-cytochrome c reductase was described (TZAGO-LOFF, FOURY and AKAI 1976). Analysis of the mitochondrially translated proteins revealed the absence in the mutant of the mitochondrial product corresponding to cytochrome...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Coruzzi G,Tzagoloff A

    更新日期:1980-08-01 00:00:00

  • Yeast frameshift suppressor mutations in the genes coding for transcription factor Mbf1p and ribosomal protein S3: evidence for autoregulation of S3 synthesis.

    abstract::The SUF13 and SUF14 genes were identified among extragenic suppressors of +1 frameshift mutations. SUF13 is synonymous with MBF1, a single-copy nonessential gene coding for a POLII transcription factor. The suf13-1 mutation is a two-nucleotide deletion in the SUF13/MBF1 coding region. A suf13::TRP1 null mutant suppres...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Hendrick JL,Wilson PG,Edelman II,Sandbaken MG,Ursic D,Culbertson MR

    更新日期:2001-03-01 00:00:00

  • Dynamic Bayesian testing of sets of variants in complex diseases.

    abstract::Rare genetic variants have recently been studied for genome-wide associations with human complex diseases. Existing rare variant methods are based on the hypothesis-testing framework that predefined variant sets need to be tested separately. The power of those methods is contingent upon accurate selection of variants ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.114.167403

    authors: Zhang Y,Ghosh S,Hakonarson H

    更新日期:2014-11-01 00:00:00

  • DAF-16-dependent suppression of immunity during reproduction in Caenorhabditis elegans.

    abstract::To further understand how the nematode Caenorhabditis elegans defends itself against pathogen attack, we analyzed enhanced pathogen resistance (epr) mutants obtained from a forward genetic screen. We also examined several well-characterized sterile mutants that exhibit an Epr phenotype. We found that sterility and pat...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.107.083923

    authors: Miyata S,Begun J,Troemel ER,Ausubel FM

    更新日期:2008-02-01 00:00:00

  • Amylase Variation in the Salt Marsh Amphipod, GAMMARUS PALUSTRIS.

    abstract::There are two common alleles at the Amylase-2 locus in populations of Gammarus palustris, the salt marsh amphipod. Intensive sampling of individuals from two localities at Jamaica Bay revealed a consistent pattern of heterozygote deficiency.-Five possible sources of heterozygote deficiency were examined in this study....

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Borowsky R,Borowsky B,Milani H,Greenberg P

    更新日期:1985-10-01 00:00:00

  • A cladistic measure of gene flow inferred from the phylogenies of alleles.

    abstract::A method for estimating the average level of gene flow among populations is introduced. The method provides an estimate of Nm, where N is the size of each local population in an island model and m is the migration rate. This method depends on knowing the phylogeny of the nonrecombining segments of DNA that are sampled...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Slatkin M,Maddison WP

    更新日期:1989-11-01 00:00:00

  • RNAi of met1 reduces DNA methylation and induces genome-specific changes in gene expression and centromeric small RNA accumulation in Arabidopsis allopolyploids.

    abstract::Changes in genome structure and gene expression have been documented in both resynthesized and natural allopolyploids that contain two or more divergent genomes. The underlying mechanisms for rapid and stochastic changes in gene expression are unknown. Arabidopsis suecica is a natural allotetraploid derived from the e...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.107.086272

    authors: Chen M,Ha M,Lackey E,Wang J,Chen ZJ

    更新日期:2008-04-01 00:00:00

  • The G-protein alpha-subunit GasC plays a major role in germination in the dimorphic fungus Penicillium marneffei.

    abstract::The opportunistic human pathogen Penicillium marneffei exhibits a temperature-dependent dimorphic switch. At 25 degrees, multinucleate, septate hyphae that can undergo differentiation to produce asexual spores (conidia) are produced. At 37 degrees hyphae undergo arthroconidiation to produce uninucleate yeast cells tha...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Zuber S,Hynes MJ,Andrianopoulos A

    更新日期:2003-06-01 00:00:00

  • Spatial autocorrelation of genotypes under directional selection.

    abstract::The spatial distributions of genetic variation under selection-mutation equilibrium within populations that have limited dispersal are investigated. The results show that directional selection with moderate strength rapidly reduces the amount of genetic structure and spatial autocorrelations far below that predicted f...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Epperson BK

    更新日期:1990-03-01 00:00:00

  • A Novel Statistical Model to Estimate Host Genetic Effects Affecting Disease Transmission.

    abstract::There is increasing recognition that genetic diversity can affect the spread of diseases, potentially affecting plant and livestock disease control as well as the emergence of human disease outbreaks. Nevertheless, even though computational tools can guide the control of infectious diseases, few epidemiological models...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.115.179853

    authors: Anacleto O,Garcia-Cortés LA,Lipschutz-Powell D,Woolliams JA,Doeschl-Wilson AB

    更新日期:2015-11-01 00:00:00

  • Genetic analysis of yeast Yip1p function reveals a requirement for Golgi-localized rab proteins and rab-Guanine nucleotide dissociation inhibitor.

    abstract::Yip1p is the first identified Rab-interacting membrane protein and the founder member of the YIP1 family, with both orthologs and paralogs found in all eukaryotic genomes. The exact role of Yip1p is unclear; YIP1 is an essential gene and defective alleles severely disrupt membrane transport and inhibit ER vesicle budd...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.104.032888

    authors: Chen CZ,Calero M,DeRegis CJ,Heidtman M,Barlowe C,Collins RN

    更新日期:2004-12-01 00:00:00

  • Linkage disequilibrium for two X-linked genes in Sardinia and its bearing on the statistical mapping of the human X chromosome.

    abstract::The distribution of four X-linked mutants (G6PD, Deutan, Protan and Xg) among lowland and once highly malarial populations of Sardinia discloses a clear-cut example of linkage disequiligrium between two of them (G6PD and Protan). In the same populations the distribution of G6PD-deficiency versus colorblindness of the ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Filippi G,Rinaldi A,Palmarino R,Seravalli E,Siniscalco M

    更新日期:1977-05-01 00:00:00

  • The Role of the UNC-82 Protein Kinase in Organizing Myosin Filaments in Striated Muscle of Caenorhabditis elegans.

    abstract::We study the mechanisms that guide the formation and maintenance of the highly ordered actin-myosin cytoskeleton in striated muscle. The UNC-82 kinase of Caenorhabditis elegans is orthologous to mammalian kinases ARK5/NUAK1 and SNARK/NUAK2. UNC-82 localizes to the M-line, and is required for proper organization of thi...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.116.193029

    authors: Schiller NR,Duchesneau CD,Lane LS,Reedy AR,Manzon ER,Hoppe PE

    更新日期:2017-03-01 00:00:00

  • Multi-trait Genome-Wide Analyses of the Brain Imaging Phenotypes in UK Biobank.

    abstract::Many genetic variants identified in genome-wide association studies (GWAS) are associated with multiple, sometimes seemingly unrelated, traits. This motivates multi-trait association analyses, which have successfully identified novel associated loci for many complex diseases. While appealing, most existing methods foc...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.120.303242

    authors: Wu C

    更新日期:2020-08-01 00:00:00

  • Temperature-sensitive pleiotropic revertants from a mutant in the arom gene cluster of Neurospora crassa.

    abstract::Genetical and biochemical studies have been performed with revertants induced in a polyaromatic mutant (No. 58) in the arom gene cluster of Neurospora crassa. In addition to complete and partial revertants able to grow on minimal at both 25 degrees and 35 degrees , temperature-sensitive revertants capable of growth on...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Case ME,Giles NH

    更新日期:1974-04-01 00:00:00

  • The phenotype of mes-2, mes-3, mes-4 and mes-6, maternal-effect genes required for survival of the germline in Caenorhabditis elegans, is sensitive to chromosome dosage.

    abstract::Mutations in mes-2, mes-3, mes-4, and mes-6 result in maternal-effect sterility: hermaphrodite offspring of mes/mes mothers are sterile because of underproliferation and death of the germ cells, as well as an absence of gametes. Mutant germ cells do not undergo programmed cell death, but instead undergo a necrotic-typ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Garvin C,Holdeman R,Strome S

    更新日期:1998-01-01 00:00:00

  • The centenary of Janssens's chiasmatype theory.

    abstract::The segregation and random assortment of characters observed by Mendel have their basis in the behavior of chromosomes in meiosis. But showing this actually to be the case requires a correct understanding of the meiotic behavior of chromosomes. This was achieved only gradually, over several decades, with much dispute ...

    journal_title:Genetics

    pub_type: 传,历史文章,杂志文章

    doi:10.1534/genetics.112.139733

    authors: Koszul R,Meselson M,Van Doninck K,Vandenhaute J,Zickler D

    更新日期:2012-06-01 00:00:00

  • Testing heterozygote excess and deficiency.

    abstract::Currently used tests of Hardy-Weinberg proportions do not take into account the nature of the alternative hypothesis, which is generally a heterozygote deficiency. Different exact tests, appropriate for small sample size and large number of alleles, are proposed in this perspective, and their properties are evaluated ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Rousset F,Raymond M

    更新日期:1995-08-01 00:00:00

  • Bayesian mapping of genomewide interacting quantitative trait loci for ordinal traits.

    abstract::Development of statistical methods and software for mapping interacting QTL has been the focus of much recent research. We previously developed a Bayesian model selection framework, based on the composite model space approach, for mapping multiple epistatic QTL affecting continuous traits. In this study we extend the ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.107.071142

    authors: Yi N,Banerjee S,Pomp D,Yandell BS

    更新日期:2007-07-01 00:00:00

  • Functional redundancy within roX1, a noncoding RNA involved in dosage compensation in Drosophila melanogaster.

    abstract::Drosophila melanogaster males dosage compensate by twofold upregulation of the expression of genes on their single X chromosome. This process requires at least five proteins and two noncoding RNAs, roX1 and roX2, which paint the male X chromosome. We used a deletion analysis to search for functional RNA domains within...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Stuckenholz C,Meller VH,Kuroda MI

    更新日期:2003-07-01 00:00:00

  • Nearly identical paralogs: implications for maize (Zea mays L.) genome evolution.

    abstract::As an ancient segmental tetraploid, the maize (Zea mays L.) genome contains large numbers of paralogs that are expected to have diverged by a minimum of 10% over time. Nearly identical paralogs (NIPs) are defined as paralogous genes that exhibit > or = 98% identity. Sequence analyses of the "gene space" of the maize i...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.106.064006

    authors: Emrich SJ,Li L,Wen TJ,Yandeau-Nelson MD,Fu Y,Guo L,Chou HH,Aluru S,Ashlock DA,Schnable PS

    更新日期:2007-01-01 00:00:00