Molecular characterization of tol, a mediator of mating-type-associated vegetative incompatibility in Neurospora crassa.

Abstract:

:The mating-type locus in the haploid filamentous fungus, Neurospora crassa, controls mating and sexual development. The fusion of reproductive structures of opposite mating type, A and a, is required to initiate sexual reproduction. However, the fusion of hyphae of opposite mating type during vegetative growth results in growth inhibition and cell death, a process that is mediated by the tol locus. Mutations in tol are recessive and suppress mating-type-associated heterokaryon incompatibility. In this study, we describe the cloning and characterization of tol. The tol gene encodes a putative 1011-amino-acid polypeptide with a coiled-coil domain and a leucine-rich repeat. Both regions are required for tol activity. Repeat-induced point mutations in tol result in mutants that are wild type during vegetative growth and sexual reproduction, but that allow opposite mating-type individuals to form a vigorous heterokaryon. Transcript analyses show that tol mRNA is present during vegetative growth but absent during a cross. These data suggest that tol transcription is repressed to allow the coexistence of opposite mating-type nuclei during the sexual reproductive phase. tol is expressed in a mat A, mat a, A/a partial diploid and in a mating-type deletion strain, indicating that MAT A-1 and MAT a-1 are not absolutely required for transcription or repression of tol. These data suggest that TOL may rather interact with MAT A-1 and/or MAT a-1 (or downstream products) to form a death-triggering complex.

journal_name

Genetics

journal_title

Genetics

authors

Shiu PK,Glass NL

subject

Has Abstract

pub_date

1999-02-01 00:00:00

pages

545-55

issue

2

eissn

0016-6731

issn

1943-2631

journal_volume

151

pub_type

杂志文章

相关文献

GENETICS文献大全
  • Genetic Change in Mutations at the T/t-Locus in the Mouse.

    abstract::Recessive lethal or semilethal alleles at the T/t locus in the mouse generate new t-variants, with characteristics different from the parent allele at a rate of about 10(-3). Almost invariably the variant chromosome carries marker genes derived from the opposite parental chromosome. New t-mutations obtained in this wa...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Bennett D,Dunn LC,Artzt K

    更新日期:1976-06-01 00:00:00

  • A genome-wide departure from the standard neutral model in natural populations of Drosophila.

    abstract::We analyze nucleotide polymorphism data for a large number of loci in areas of normal to high recombination in Drosophila melanogaster and D. simulans (24 and 16 loci, respectively). We find a genome-wide, systematic departure from the neutral expectation for a panmictic population at equilibrium in natural population...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Andolfatto P,Przeworski M

    更新日期:2000-09-01 00:00:00

  • Repeated Duplication of Argonaute2 Is Associated with Strong Selection and Testis Specialization in Drosophila.

    abstract::Argonaute2 (Ago2) is a rapidly evolving nuclease in the Drosophila melanogaster RNA interference (RNAi) pathway that targets viruses and transposable elements in somatic tissues. Here we reconstruct the history of Ago2 duplications across the D. obscura group and use patterns of gene expression to infer new functional...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.116.192336

    authors: Lewis SH,Webster CL,Salmela H,Obbard DJ

    更新日期:2016-10-01 00:00:00

  • The maize unstable factor for orange1 is a dominant epigenetic modifier of a tissue specifically silent allele of pericarp color1.

    abstract::We have characterized Unstable factor for orange1 (Ufo1), a dominant, allele-specific modifier of expression of the maize pericarp color1 (p1) gene. The p1 gene encodes an Myb-homologous transcriptional activator of genes required for biosynthesis of red phlobaphene pigments. The P1-wr allele specifies colorless kerne...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Chopra S,Cocciolone SM,Bushman S,Sangar V,McMullen MD,Peterson T

    更新日期:2003-03-01 00:00:00

  • Genetic linkage maps of the red flour beetle, Tribolium castaneum, based on bacterial artificial chromosomes and expressed sequence tags.

    abstract::A genetic linkage map was constructed in a backcross family of the red flour beetle, Tribolium castaneum, based largely on sequences from bacterial artificial chromosome (BAC) ends and untranslated regions from random cDNA's. In most cases, dimorphisms were detected using heteroduplex or single-strand conformational p...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.104.032227

    authors: Lorenzen MD,Doyungan Z,Savard J,Snow K,Crumly LR,Shippy TD,Stuart JJ,Brown SJ,Beeman RW

    更新日期:2005-06-01 00:00:00

  • Power evaluations for family-based tests of association with incomplete parental genotypes.

    abstract::While a variety of methods have been developed to deal with incomplete parental genotype information in family-based association tests, sampling design issues with incomplete parental genotype data still have not received much attention. In this article, we present simulation studies with four genetic models and vario...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Yang Q,Xu X,Laird N

    更新日期:2003-05-01 00:00:00

  • Molecular evolution of genes controlling petal and stamen development: duplication and divergence within the APETALA3 and PISTILLATA MADS-box gene lineages.

    abstract::The specification of floral organ identity in the higher dicots depends on the function of a limited set of homeotic genes, many of them members of the MADS-box gene family. Two such genes, APETALA3 (AP3) and PISTILLATA (PI), are required for petal and stamen identity in Arabidopsis; their orthologs in Antirrhinum exh...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Kramer EM,Dorit RL,Irish VF

    更新日期:1998-06-01 00:00:00

  • Spermiogenesis initiation in Caenorhabditis elegans involves a casein kinase 1 encoded by the spe-6 gene.

    abstract::Immature spermatids from Caenorhabditis elegans are stimulated by an external activation signal to reorganize their membranes and cytoskeleton to form crawling spermatozoa. This rapid maturation, termed spermiogenesis, occurs without any new gene expression. To better understand this signal transduction pathway, we is...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Muhlrad PJ,Ward S

    更新日期:2002-05-01 00:00:00

  • The effective size of populations infected with cytoplasmic sex-ratio distorters.

    abstract::Many arthropod species are infected with maternally inherited endosymbionts that induce a shift in the sex ratio of their hosts by feminizing or killing males (cytoplasmic sex-ratio distorters, or SRDs). These endosymbionts can have profound impacts on evolutionary processes of their hosts. Here, I derive analytical e...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.110.120014

    authors: Engelstädter J

    更新日期:2010-09-01 00:00:00

  • Sequencing complex diseases With HapMap.

    abstract::Determining the patterns of DNA sequence variation in the human genome is a useful first step toward identifying the genetic basis of a common disease. A haplotype map (HapMap), aimed at describing these variation patterns across the entire genome, has been recently developed by the International HapMap Consortium. In...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.104.029603

    authors: Liu T,Johnson JA,Casella G,Wu R

    更新日期:2004-09-01 00:00:00

  • Frequency-dependent selection and the maintenance of genetic variation: exploring the parameter space of the multiallelic pairwise interaction model.

    abstract::When individuals' fitnesses depend on the genetic composition of the population in which they are found, selection is then frequency dependent. Frequency-dependent selection (FDS) is often invoked as a heuristic explanation for the maintenance of large numbers of alleles at a locus. The pairwise interaction model is a...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.107.073072

    authors: Trotter MV,Spencer HG

    更新日期:2007-07-01 00:00:00

  • The next generation of molecular markers from massively parallel sequencing of pooled DNA samples.

    abstract::Next generation sequencing (NGS) is about to revolutionize genetic analysis. Currently NGS techniques are mainly used to sequence individual genomes. Due to the high sequence coverage required, the costs for population-scale analyses are still too high to allow an extension to nonmodel organisms. Here, we show that NG...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.110.114397

    authors: Futschik A,Schlötterer C

    更新日期:2010-09-01 00:00:00

  • Genome scans for transmission ratio distortion regions in mice.

    abstract::Transmission ratio distortion (TRD) is the departure from the expected genotypic frequencies under Mendelian inheritance. This departure can be due to multiple physiological mechanisms during gametogenesis, fertilization, fetal and embryonic development, and early neonatal life. Although a few TRD loci have been repor...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.111.135988

    authors: Casellas J,Gularte RJ,Farber CR,Varona L,Mehrabian M,Schadt EE,Lusis AJ,Attie AD,Yandell BS,Medrano JF

    更新日期:2012-05-01 00:00:00

  • The isolation of mms- and histidine-sensitive mutants in Neurospora crassa.

    abstract::A simple method of replica plating has been used to isolate mutants of Neurospora crassa that have increased sensitivity to methyl methanesulfonate (MMS) and/or to histidine. Twelve mutants with increased sensitivity to MMS and one mutant with increased sensitivity to histidine showed Mendelian segregation of the muta...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Delange AM,Mishra NC

    更新日期:1981-02-01 00:00:00

  • Intragenic suppression at the b2 locus in Ascobolus immersus. I. Identification of three distinct groups of suppression.

    abstract::A reversion study of EMS- or ICR170-induced ascospore color mutants in Ascobolus immersus is reported. Twenty-three new intragenic suppressors were isolated within the b2 locus. These are localized within three distinct groups on a genetic fine-structure map containing 21 identifiable sites. The pattern of reversion i...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Leblon G,Paquette N

    更新日期:1978-11-01 00:00:00

  • An implanted recombination hot spot stimulates recombination and enhances sister chromatid cohesion of heterologous YACs during yeast meiosis.

    abstract::Heterologous yeast artificial chromosomes (YACs) do not recombine with each other and missegregate in 25% of meiosis I events. Recombination hot spots in the yeast Saccharomyces cerevisiae have previously been shown to be associated with sites of meiosis-induced double-strand breaks (DSBs). A 6-kb fragment containing ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Sears DD,Hieter P,Simchen G

    更新日期:1994-12-01 00:00:00

  • Deep haplotype divergence and long-range linkage disequilibrium at xp21.1 provide evidence that humans descend from a structured ancestral population.

    abstract::Fossil evidence links human ancestry with populations that evolved from modern gracile morphology in Africa 130,000-160,000 years ago. Yet fossils alone do not provide clear answers to the question of whether the ancestors of all modern Homo sapiens comprised a single African population or an amalgamation of distinct ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.041095

    authors: Garrigan D,Mobasher Z,Kingan SB,Wilder JA,Hammer MF

    更新日期:2005-08-01 00:00:00

  • Imputing Genotypes in Biallelic Populations from Low-Coverage Sequence Data.

    abstract::Low-coverage next-generation sequencing methodologies are routinely employed to genotype large populations. Missing data in these populations manifest both as missing markers and markers with incomplete allele recovery. False homozygous calls at heterozygous sites resulting from incomplete allele recovery confound man...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.115.182071

    authors: Fragoso CA,Heffelfinger C,Zhao H,Dellaporta SL

    更新日期:2016-02-01 00:00:00

  • Robust forward simulations of recurrent hitchhiking.

    abstract::Evolutionary forces shape patterns of genetic diversity within populations and contribute to phenotypic variation. In particular, recurrent positive selection has attracted significant interest in both theoretical and empirical studies. However, most existing theoretical models of recurrent positive selection cannot e...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.113.156935

    authors: Uricchio LH,Hernandez RD

    更新日期:2014-05-01 00:00:00

  • Clonal mosaic analysis of EMPTY PERICARP2 reveals nonredundant functions of the duplicated HEAT SHOCK FACTOR BINDING PROTEINs during maize shoot development.

    abstract::The paralogous maize proteins EMPTY PERICARP2 (EMP2) and HEAT SHOCK FACTOR BINDING PROTEIN2 (HSBP2) each contain a single recognizable motif: the coiled-coil domain. EMP2 and HSBP2 accumulate differentially during maize development and heat stress. Previous analyses revealed that EMP2 is required for regulation of hea...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.104.026575

    authors: Fu S,Scanlon MJ

    更新日期:2004-07-01 00:00:00

  • Multiple mechanisms for degradation of bacteriophage T4 soc mRNA.

    abstract::The dmd gene of bacteriophage T4 is required for regulation of mRNA stability in a stage-dependent manner during infection. When this gene is mutated, late genes are globally silenced because of rapid degradation of mRNAs. To investigate the mechanism of such mRNA degradation, we analyzed the late gene soc transcripts...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Kai T,Yonesaki T

    更新日期:2002-01-01 00:00:00

  • fumble encodes a pantothenate kinase homolog required for proper mitosis and meiosis in Drosophila melanogaster.

    abstract::A number of fundamental processes comprise the cell division cycle, including spindle formation, chromosome segregation, and cytokinesis. Our current understanding of these processes has benefited from the isolation and analysis of mutants, with the meiotic divisions in the male germline of Drosophila being particular...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Afshar K,Gönczy P,DiNardo S,Wasserman SA

    更新日期:2001-03-01 00:00:00

  • Analysis of the albino-locus region of the mouse: IV. Characterization of 34 deficiencies.

    abstract::Thirty-four independent nonviable c-locus mutations (types cal, albino lethal and cas, albino subvital), derived from radiation experiments, were tested for involvement of nearby markers tp, Mod-2, sh-1, and Hbb: 10, 22, and 2 involved, respectively, none of these markers, Mod-2 alone, and Mod-2 plus sh-1. When classi...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Russell LB,Montgomery CS,Raymer GD

    更新日期:1982-03-01 00:00:00

  • Evidence for local regulatory control of escape from imprinted X chromosome inactivation.

    abstract::X chromosome inactivation (XCI) is an epigenetic process that almost completely inactivates one of two X chromosomes in somatic cells of mammalian females. A few genes are known to escape XCI and the mechanism for this escape remains unclear. Here, using mouse trophoblast stem (TS) cells, we address whether particular...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.114.162800

    authors: Mugford JW,Starmer J,Williams RL Jr,Calabrese JM,Mieczkowski P,Yee D,Magnuson T

    更新日期:2014-06-01 00:00:00

  • Narrowing the critical regions for mouse t complex transmission ratio distortion factors by use of deletions.

    abstract::Previously a deletion in mouse chromosome 17, T(22H), was shown to behave like a t allele of the t complex distorter gene Tcd1, and this was attributed to deletion of this locus. Seven further deletions are studied here, with the aim of narrowing the critical region in which Tcd1 must lie. One deletion, T(30H), togeth...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Lyon MF,Schimenti JC,Evans EP

    更新日期:2000-06-01 00:00:00

  • Preferential mating in symmetric multilocus systems: stability conditions of the central equilibrium.

    abstract::Several multilocus models that incorporate both preferential mating and viability selection are studied. Specifically, a class of symmetric heterozygosity models are considered that assign individuals to phenotypic classes according to which loci are in heterozygous state regardless of the actual allelic content. Othe...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Karlin S,Raper J

    更新日期:1982-01-01 00:00:00

  • Regulation of ribosome biogenesis by nucleostemin 3 promotes local and systemic growth in Drosophila.

    abstract::Nucleostemin 3 (NS3) is an evolutionarily conserved protein with profound roles in cell growth and viability. Here we analyze cell-autonomous and non-cell-autonomous growth control roles of NS3 in Drosophila and demonstrate its GTPase activity using genetic and biochemical assays. Two null alleles of ns3, and RNAi, de...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.112.149104

    authors: Hartl TA,Ni J,Cao J,Suyama KL,Patchett S,Bussiere C,Gui DY,Tang S,Kaplan DD,Fish M,Johnson AW,Scott MP

    更新日期:2013-05-01 00:00:00

  • A key transcription cofactor on the nascent sex chromosomes of European tree frogs (Hyla arborea).

    abstract::We show that MED15, a key component of the transcription complex Mediator, lies within the nonrecombining segment of nascent sex chromosomes in the male-heterogametic Hyla arborea. Both X and Y alleles are expressed during embryonic development and differ by three frame-preserving indels (eight amino acids in total) w...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.108.090746

    authors: Niculita-Hirzel H,Stöck M,Perrin N

    更新日期:2008-07-01 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

  • Conserved WCPL and CX4C domains mediate several mating adhesin interactions in Saccharomyces cerevisiae.

    abstract::Several adhesins are induced by pheromones during mating in Saccharomyces cerevisiae, including Aga1p, Aga2p, Sag1p (Agalpha1p), and Fig2p. These four proteins all participate in or influence a well-studied agglutinin interaction mediated by Aga1p-Aga2p complexes and Sag1p; however, they also play redundant and essent...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.108.100073

    authors: Huang G,Dougherty SD,Erdman SE

    更新日期:2009-05-01 00:00:00