Los1p, involved in yeast pre-tRNA splicing, positively regulates members of the SOL gene family.

Abstract:

:To understand the role of Los1p in pre-tRNA splicing, we sought los1 multicopy suppressors. We found SOL1 that suppresses both point and null LOS1 mutations. Since, when fused to the Ga14p DNA-binding domain, Los1p activates transcription, we tested whether Los1p regulates SOL1. We found that las1 mutants have depleted levels of SOL1 mRNA and Sol1p. Thus, LOS1 appears to positively regulate SOL1. SOL1 belongs to a multigene family with at least two additional members, SOL2 and SOL3. Sol proteins have extensive similarity to an unusual group of glucose-6-phosphate dehydrogenases. As the similarities are restricted to areas separate from the catalytic domain, these G6PDs may have more than one function. The SOL family appears to be unessential since cells with a triple disruption of all three SOL genes are viable. SOL gene disruptions negatively affect tRNA-mediated nonsense suppression and the severity increases with the number of mutant SOL genes. However, tRNA levels do not vary with either multicopy SOL genes or with SOL disruptions. Therefore, the Sol proteins affect tRNA expression/ function at steps other than transcription or splicing. We propose that LOS1 regulates gene products involved in tRNA expression/function as well as pre-tRNA splicing.

journal_name

Genetics

journal_title

Genetics

authors

Shen WC,Stanford DR,Hopper AK

subject

Has Abstract

pub_date

1996-06-01 00:00:00

pages

699-712

issue

2

eissn

0016-6731

issn

1943-2631

journal_volume

143

pub_type

杂志文章

相关文献

GENETICS文献大全
  • Identification of mutations in three genes that interact with zeste in the control of white gene expression in Drosophila melanogaster.

    abstract::Three previously described genes, enhancer of yellow, 1, 2 and 3, are shown to cooperate with the zeste gene in the control of white gene expression. The mutations e(y)1u1, e(y)3u1, and to a lesser extent e(y)2u1, enhance the effect of the zeste null allele zv77h. Different combinations of e(y)1u1, e(y)2u1 and e(y)3u1...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Georgiev PG

    更新日期:1994-11-01 00:00:00

  • Spatial structure of two-locus genotypes under isolation by distance.

    abstract::Extensive Monte Carlo simulations are conducted of spatial distributions of two-locus genotypes in large, continuous populations under isolation by distance models. The results show that substantial patches of double homozygotes are present in the spatial structures, even when loci are unlinked. The stochastic spread ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Epperson BK

    更新日期:1995-05-01 00:00:00

  • Bipartite structure of the 5S ribosomal gene family in a Drosophila melanogaster strain, and its evolutionary implications.

    abstract::Knowledge of multigenic family organization should provide insight into their mode of evolution. Accordingly, we characterized the 5S ribosomal gene family in the Drosophila melanogaster strain ry506. The 5S genes in this strain display a striking HindIII restriction difference compared to the "standard" D. melanogast...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Samson ML,Wegnez M

    更新日期:1988-04-01 00:00:00

  • Genetic and physical analysis of the M26 recombination hotspot of Schizosaccharomyces pombe.

    abstract::The ade6-M26 mutation of Schizosaccharomyces pombe has previously been reported to stimulate ade6 intragenic meiotic recombination. We report here that the ade6-M26 mutation is a single G----T nucleotide change, that M26 stimulated recombination within ade6 but not at other distinct loci, and that M26 stimulated meiot...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Ponticelli AS,Sena EP,Smith GR

    更新日期:1988-07-01 00:00:00

  • Electrophysiological Alterations of Pyramidal Cells and Interneurons of the CA1 Region of the Hippocampus in a Novel Mouse Model of Dravet Syndrome.

    abstract::Dravet syndrome is a developmental epileptic encephalopathy caused by pathogenic variation in SCN1A To characterize the pathogenic substitution (p.H939R) of a local individual with Dravet syndrome, fibroblast cells from the individual were reprogrammed to pluripotent stem cells and differentiated into neurons. Sodium ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.120.303399

    authors: Dyment DA,Schock SC,Deloughery K,Tran MH,Ure K,Nutter LMJ,Creighton A,Yuan J,Banderali U,Comas T,Baumann E,Jezierski A,Care4Rare Canada Consortium,.,Boycott KM,Mackenzie AE,Martina M

    更新日期:2020-08-01 00:00:00

  • Identification and characterization of Schizosaccharomyces pombe asp1(+), a gene that interacts with mutations in the Arp2/3 complex and actin.

    abstract::The Arp2/3 complex is an essential component of the actin cytoskeleton in yeast and is required for the movement of actin patches. In an attempt to identify proteins that interact with this complex in the fission yeast Schizosaccharomyces pombe, we sought high-copy suppressors of the S. pombe arp3-c1 mutant, and have ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Feoktistova A,McCollum D,Ohi R,Gould KL

    更新日期:1999-07-01 00:00:00

  • Arabidopsis SHORT INTEGUMENTS 2 is a mitochondrial DAR GTPase.

    abstract::The Arabidopsis short integuments 2-1 (sin2-1) mutant produces ovules with short integuments due to early cessation of cell division in these structures. SIN2 was isolated and encodes a putative GTPase sharing features found in the novel DAR GTPase family. DAR proteins share a signature DAR motif and a unique arrangem...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.106.060657

    authors: Hill TA,Broadhvest J,Kuzoff RK,Gasser CS

    更新日期:2006-10-01 00:00:00

  • Toward a marker-dense meiotic map of the potato genome: lessons from linkage group I.

    abstract::Segregation data were obtained for 1260 potato linkage group I-specific AFLP loci from a heterozygous diploid potato population. Analytical tools that identified potential typing errors and/or inconsistencies in the data and that assembled cosegregating markers into bins were applied. Bins contain multiple-marker data...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Isidore E,van Os H,Andrzejewski S,Bakker J,Barrena I,Bryan GJ,Caromel B,van Eck H,Ghareeb B,de Jong W,van Koert P,Lefebvre V,Milbourne D,Ritter E,van der Voort JR,Rousselle-Bourgeois F,van Vliet J,Waugh R

    更新日期:2003-12-01 00:00:00

  • Cytogenetic analysis of segregation distortion in Drosophila melanogaster: the cytological organization of the Responder (Rsp) locus.

    abstract::The segregation distortion phenomenon occurs in Drosophila melanogaster males carrying an SD second chromosome and an SD+ homolog. In such males the SD chromosome is transmitted to the progeny more frequently than the expected 50% because of an abnormal differentiation of the SD+-bearing sperms. Three major loci are i...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Pimpinelli S,Dimitri P

    更新日期:1989-04-01 00:00:00

  • Essential, overlapping and redundant roles of the Drosophila protein phosphatase 1 alpha and 1 beta genes.

    abstract::Protein serine/threonine phosphatase type 1 (PP1) has been found in all eukaryotes examined to date and is involved in the regulation of many cellular functions, including glycogen metabolism, muscle contraction, and mitosis. In Drosophila, four genes code for the catalytic subunit of PP1 (PP1c), three of which belong...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.106.069914

    authors: Kirchner J,Gross S,Bennett D,Alphey L

    更新日期:2007-05-01 00:00:00

  • P element-mediated in vivo deletion analysis of white-apricot: deletions between direct repeats are strongly favored.

    abstract::We have isolated and characterized deletions arising within a P transposon, P[hswa], in the presence of P transposase. P[hswa] carries white-apricot (wa) sequences, including a complete copia element, under the control of an hsp70 promoter, and resembles the original wa allele in eye color phenotype. In the presence o...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Kurkulos M,Weinberg JM,Roy D,Mount SM

    更新日期:1994-03-01 00:00:00

  • Multiple Transcriptional and Post-transcriptional Pathways Collaborate to Control Sense and Antisense RNAs of Tf2 Retroelements in Fission Yeast.

    abstract::Retrotransposons are mobile genetic elements that colonize eukaryotic genomes by replicating through an RNA intermediate. As retrotransposons can move within the host genome, defense mechanisms have evolved to repress their potential mutagenic activities. In the fission yeast Schizosaccharomyces pombe, the mRNA of Tf2...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.116.193870

    authors: Mallet PL,Larochelle M,Bachand F

    更新日期:2017-02-01 00:00:00

  • A random mutagenesis approach to isolate dominant-negative yeast sec1 mutants reveals a functional role for domain 3a in yeast and mammalian Sec1/Munc18 proteins.

    abstract::SNAP receptor (SNARE) and Sec1/Munc18 (SM) proteins are required for all intracellular membrane fusion events. SNAREs are widely believed to drive the fusion process, but the function of SM proteins remains unclear. To shed light on this, we screened for dominant-negative mutants of yeast Sec1 by random mutagenesis of...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.108.090423

    authors: Boyd A,Ciufo LF,Barclay JW,Graham ME,Haynes LP,Doherty MK,Riesen M,Burgoyne RD,Morgan A

    更新日期:2008-09-01 00:00:00

  • Nitrogen starvation and TorC1 inhibition differentially affect nuclear localization of the Gln3 and Gat1 transcription factors through the rare glutamine tRNACUG in Saccharomyces cerevisiae.

    abstract::A leucine, leucyl-tRNA synthetase-dependent pathway activates TorC1 kinase and its downstream stimulation of protein synthesis, a major nitrogen consumer. We previously demonstrated, however, that control of Gln3, a transcription activator of catabolic genes whose products generate the nitrogenous precursors for prote...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.114.173831

    authors: Tate JJ,Rai R,Cooper TG

    更新日期:2015-02-01 00:00:00

  • Organization of the Rudimentary Wing Locus in DROSOPHILA MELANOGASTER. I. the Isolation and Partial Characterization of Mutants Induced with Ethyl Methanesulfonate, Icr-170 and X Rays.

    abstract::New rudimentary (r) mutants have been isolated following mutagenesis with ethyl methanesulfonate (r(LE)), ICR-170 (r(LI)) and X rays (r(LX)). From wing phenotype measurements on homoallelic females, it has been shown that the r(LE) mutant series includes several leaky alleles, as well as alleles that produce moderate ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Rawls JM,Porter LA

    更新日期:1979-09-01 00:00:00

  • Induction of Ty recombination in yeast by cDNA and transcription: role of the RAD1 and RAD52 genes.

    abstract::In the yeast Saccharomyces cerevisiae ectopic recombination has been shown to occur at high frequencies for artificially created repeats, but at relatively low frequencies for a natural family of repeated sequences, the Ty family. Little is known about the mechanism(s) that prevent recombination between repeated seque...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Nevo-Caspi Y,Kupiec M

    更新日期:1996-11-01 00:00:00

  • Repair replication and photorepair of DNA in larvae of Drosophila melanogaster.

    abstract::Repair replication of DNA has been studied in first instar larvae of Drosophila melanogaster with isopycnic centrifugation techniques. Larvae were fed BUdR, FUdR, streptomycin, penicillin, and Fungazone for two to four hours prior to exposure to UV, X-rays, MMS, or EMS. Feeding was continued for four hours in the pres...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Boyd JB,Presley JM

    更新日期:1974-08-01 00:00:00

  • Diverse domains of THREAD/DIAP1 are required to inhibit apoptosis induced by REAPER and HID in Drosophila.

    abstract::Significant amounts of apoptosis take place during Drosophila development. The proapoptotic genes reaper (rpr), grim, and head involution defective (hid) are required for virtually all embryonic apoptosis. The proteins encoded by these genes share a short region of homology at their amino termini. The Drosophila IAP h...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Lisi S,Mazzon I,White K

    更新日期:2000-02-01 00:00:00

  • Mutations in the extra sex combs and Enhancer of Polycomb genes increase homologous recombination in somatic cells of Drosophila melanogaster.

    abstract::We found that heterozygous mutant alleles of E(Pc) and esc increased homologous recombination from an allelic template in somatic cells in a P-element-induced double-strand break repair assay. Flies heterozygous for mutant alleles of these genes showed increased genome stability and decreased levels of apoptosis in im...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.042473

    authors: Holmes AM,Weedmark KA,Gloor GB

    更新日期:2006-04-01 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

  • A deficiency screen for dominant suppressors of telomeric silencing in Drosophila.

    abstract::Heterochromatin is a specialized chromatin structure in chromosomal regions associated with repeated DNA sequences and low concentrations of genes. Formation of heterochromatin is determined in large part by enzymes that modify histones and structural proteins that bind to these modified histones in a cooperative fash...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.104.030676

    authors: Mason JM,Ransom J,Konev AY

    更新日期:2004-11-01 00:00:00

  • Switching of a mating-type a mutant allele in budding yeast Saccharomyces cerevisiae.

    abstract::Aimed at investigating the recovery of a specific mutant allele of the mating type locus (MAT) by switching a defective MAT allele, these experiments provide information bearing on several models proposed for MAT interconversion in bakers yeast, Saccharomyces cerevisiae. Hybrids between heterothallic (ho) cells carryi...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Klar AJ,Fogel S,Radin DN

    更新日期:1979-07-01 00:00:00

  • Analysis of conditional genetic effects and variance components in developmental genetics.

    abstract::A genetic model with additive-dominance effects and genotype x environment interactions is presented for quantitative traits with time-dependent measures. The genetic model for phenotypic means at time t conditional on phenotypic means measured at previous time (t-1) is defined. Statistical methods are proposed for an...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Zhu J

    更新日期:1995-12-01 00:00:00

  • Selection on X-linked genes during speciation in the Drosophila athabasca complex.

    abstract::We present the results of a restriction site survey of variation at five loci in Drosophila athabasca, complimenting a previous study of the period locus. There is considerably greater differentiation between the three semispecies of D. athabasca at the period locus and two other X-linked genes (no-on-transient-A and ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Ford MJ,Aquadro CF

    更新日期:1996-10-01 00:00:00

  • An Allosteric Network for Spliceosome Activation Revealed by High-Throughput Suppressor Analysis in Saccharomyces cerevisiae.

    abstract::Selection of suppressor mutations that correct growth defects caused by substitutions in an RNA or protein can reveal functionally important molecular structures and interactions in living cells. This approach is particularly useful for the study of complex biological pathways involving many macromolecules, such as pr...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.119.301922

    authors: Brow DA

    更新日期:2019-05-01 00:00:00

  • The Saccharomyces cerevisiae PRM1 homolog in Neurospora crassa is involved in vegetative and sexual cell fusion events but also has postfertilization functions.

    abstract::Cell-cell fusion is essential for a variety of developmental steps in many eukaryotic organisms, during both fertilization and vegetative cell growth. Although the molecular mechanisms associated with intracellular membrane fusion are well characterized, the molecular mechanisms of plasma membrane merger between cells...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.108.096149

    authors: Fleissner A,Diamond S,Glass NL

    更新日期:2009-02-01 00:00:00

  • Weakener of white (Wow), a gene that modifies the expression of the white eye color locus and that suppresses position effect variegation in Drosophila melanogaster.

    abstract::A locus is described in Drosophila melanogaster that modifies the expression of the white eye color gene. This trans-acting modifier reduces the expression of the white gene in the eye, but elevates the expression in other adult tissues. Because of the eye phenotype in which the expression of white is lessened but not...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Birchler JA,Bhadra U,Rabinow L,Linsk R,Nguyen-Huynh AT

    更新日期:1994-08-01 00:00:00

  • Phenotypic plasticity and genotype by environment interaction for olfactory behavior in Drosophila melanogaster.

    abstract::Genotype by environment interactions (GEI) play a major part in shaping the genetic architecture of quantitative traits and are confounding factors in genetic studies, for example, in attempts to associate genetic variation with disease susceptibility. It is generally not known what proportion of phenotypic variation ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.108.086769

    authors: Sambandan D,Carbone MA,Anholt RR,Mackay TF

    更新日期:2008-06-01 00:00:00

  • UV- and gamma-radiation sensitive mutants of Arabidopsis thaliana.

    abstract::Arabidopsis seedlings repair UV-induced DNA damage via light-dependent and independent pathways. The mechanism of the "dark repair" pathway is still unknown. To determine the number of genes required for dark repair and to investigate the substrate-specificity of this process we isolated mutants with enhanced sensitiv...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Jiang CZ,Yen CN,Cronin K,Mitchell D,Britt AB

    更新日期:1997-11-01 00:00:00

  • Molecular determinants of sporulation in Ashbya gossypii.

    abstract::Regulation of development and entry into sporulation is critical for fungi to ensure survival of unfavorable environmental conditions. Here we present an analysis of gene sets regulating sporulation in the homothallic ascomycete Ashbya gossypii. Deletion of components of the conserved pheromone/starvation MAP kinase c...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.113.151019

    authors: Wasserstrom L,Lengeler KB,Walther A,Wendland J

    更新日期:2013-09-01 00:00:00