The Germline-Specific Factor OEF-1 Facilitates Coordinated Progression Through Germ Cell Development in Caenorhabditis elegans

No abstract is available for this paper.

• Publication year

  2017

• Venue

  Genetics

• Publication date

  2017-11-22

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1534/genetics.117.1123PMID 29167199PMCID PMC5788521
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Analysis of the C. elegans Germline Stem Cell Pool.

  2017cited by this paper
• X Chromosome Crossover Formation and Genome Stability in Caenorhabditis elegans Are Independently Regulated by xnd-1

  2016cited by this paper
• Stable Caenorhabditis elegans chromatin domains separate broadly expressed and developmentally regulated genes

  2016cited by this paper
• Zygotic Genome Activation Triggers Chromosome Damage and Checkpoint Signaling in C. elegans Primordial Germ Cells.

  2015cited by this paper
• CSR-1 and P granules suppress sperm-specific transcription in the C. elegans germline

  2015cited by this paper
• Dramatic Enhancement of Genome Editing by CRISPR/Cas9 Through Improved Guide RNA Design

  2015cited by this paper
• Repression of somatic cell fate in the germline

  2015cited by this paper
• Direct Visualization Reveals Kinetics of Meiotic Chromosome Synapsis.

  2015cited by this paper
• A New Dataset of Spermatogenic vs. Oogenic Transcriptomes in the Nematode Caenorhabditis elegans

  2014influential reference
• Scalable and versatile genome editing using linear DNAs with micro-homology to Cas9 sites in C. elegans

  2014cited by this paper
• Translational Control of the Oogenic Program by Components of OMA Ribonucleoprotein Particles in Caenorhabditis elegans

  2014cited by this paper
• Regulatory analysis of the C. elegans genome with spatiotemporal resolution

  2014cited by this paper
• Scalable and Versatile Genome Editing Using Linear DNAs with Microhomology to Cas9 Sites in Caenorhabditis elegans

  2014cited by this paper
• The C. elegans SNAPc component SNPC-4 coats piRNA domains and is globally required for piRNA abundance.

  2014cited by this paper
• Germ cell specification.

  2013cited by this paper
• The Ccr4–Not deadenylase complex constitutes the main poly(A) removal activity in C. elegans

  2013cited by this paper
• RSR-2, the Caenorhabditis elegans Ortholog of Human Spliceosomal Component SRm300/SRRM2, Regulates Development by Influencing the Transcriptional Machinery

  2013cited by this paper
• Resource A Genome-Scale Resource for In Vivo Tag-Based Protein Function Exploration in C . elegans

  2012cited by this paper
• Crossover Distribution and Frequency Are Regulated by him-5 in Caenorhabditis elegans

  2012cited by this paper
• Single molecule fluorescent in situ hybridization (smFISH) of C. elegans worms and embryos.

  2012cited by this paper
• Antagonism between MES-4 and Polycomb repressive complex 2 promotes appropriate gene expression in C. elegans germ cells.

  2012cited by this paper
• Genetics of germ cell development

  2012cited by this paper
• Diverse transcription factor binding features revealed by genome-wide ChIP-seq in C. elegans.

  2011cited by this paper
• The chromodomain protein MRG-1 facilitates SC-independent homologous pairing during meiosis in Caenorhabditis elegans.

  2011cited by this paper
• RSBP-1 Is a Membrane-targeting Subunit Required by the Gαq-specific But Not the Gαo-specific R7 Regulator of G protein Signaling in Caenorhabditis elegans

  2010cited by this paper
• xnd-1 Regulates the Global Recombination Landscape in C. elegans

  2010cited by this paper
• The Histone H3K36 Methyltransferase MES-4 Acts Epigenetically to Transmit the Memory of Germline Gene Expression to Progeny

  2010cited by this paper
• Cytological analysis of meiosis in Caenorhabditis elegans.

  2009cited by this paper
• Germline survival and apoptosis.

  2008cited by this paper
• Analysis of the C. elegans germline stem cell region.

  2008cited by this paper
• Sticky fingers: zinc-fingers as protein-recognition motifs.

  2007cited by this paper
• Controls of germline stem cells, entry into meiosis, and the sperm/oocyte decision in Caenorhabditis elegans.

  2007cited by this paper
• A family of zinc-finger proteins is required for chromosome-specific pairing and synapsis during meiosis in C. elegans.

  2006cited by this paper
• C. elegans DAF-18/PTEN mediates nutrient-dependent arrest of cell cycle and growth in the germline.

  2006cited by this paper
• Cellular analyses of the mitotic region in the Caenorhabditis elegans adult germ line.

  2006cited by this paper
• HIM-8 binds to the X chromosome pairing center and mediates chromosome-specific meiotic synapsis.

  2005cited by this paper
• Multiple modes of RNA recognition by zinc finger proteins.

  2005cited by this paper
• A Conserved Checkpoint Monitors Meiotic Chromosome Synapsis in Caenorhabditis elegans

  2005influential reference
• Genome-wide germline-enriched and sex-biased expression profiles in Caenorhabditis elegans

  2003cited by this paper
• [C. elegans: of neurons and genes].

  2003cited by this paper
• Caenorhabditis elegans HUS-1 is a DNA damage checkpoint protein required for genome stability and EGL-1-mediated apoptosis.

  2002cited by this paper
• X-chromosome silencing in the germline of C. elegans.

  2002cited by this paper
• Two zinc finger proteins, OMA-1 and OMA-2, are redundantly required for oocyte maturation in C. elegans.

  2001cited by this paper
• DNA recognition by Cys2His2 zinc finger proteins.

  2000cited by this paper
• DNA RECOGNITION BY Cys 2 His 2 ZINC FINGER PROTEINS

  2000cited by this paper
• Functional genomic analysis of C. elegans chromosome I by systematic RNA interference

  2000cited by this paper
• Receptor-mediated endocytosis in the Caenorhabditis elegans oocyte.

  1999influential reference
• Meiotic recombination in C. elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis.

  1998cited by this paper
• Repression of gene expression in the embryonic germ lineage of C. elegans

  1996cited by this paper
• Three genes of the MAP kinase cascade, mek-2, mpk-1/sur-1 and let-60 ras, are required for meiotic cell cycle progression in Caenorhabditis elegans.

  1995cited by this paper
• Wavelength mutations and posttranslational autoxidation of green fluorescent protein.

  1994cited by this paper
• More is not better: brood size and population growth in a self-fertilizing nematode

  1991cited by this paper
• [Genetics of Caenorhabditis elegans].

  1989cited by this paper
• Gain-of-function mutations of fem-3, a sex-determination gene in Caenorhabditis elegans.

  1987cited by this paper
• Monoclonal antibodies that recognize a polypeptide antigenic determinant shared by multiple Caenorhabditis elegans sperm-specific proteins

  1986influential reference
• Generation of asymmetry and segregation of germ-line granules in early C. elegans embryos.

  1983cited by this paper
• Intersex, a temperature-sensitive mutant of the nematode Caenorhabditis elegans.

  1978cited by this paper
• The genetics of Caenorhabditis elegans.

  1974cited by this paper
• Report 3 0 UTRs Are the Primary Regulators of Gene Expression in the C . elegans Germline

  year unknowncited by this paper

• The zinc-finger transcription factor LSL-1 is a major regulator of the germline transcriptional program in Caenorhabditis elegans

  2022cites this paper
• The zinc-finger protein OEF-1 stabilizes histone modification patterns and promotes efficient splicing in the Caenorhabditis elegans germline

  2021cites this paper
• Running title: Germline transcriptional program in C. elegans

  2021cites this paper
• Isolated C. elegans germ nuclei exhibit distinct genomic profiles of histone modification and gene expression

  2019cites this paper
• A simple and effective method to isolate germ nuclei from C. elegans for genomic assays

  2018cites this paper