Sex and the single worm: sex determination in the nematode C. elegans.

No abstract is available for this paper.

• Publication year

  1999

• Venue

  Mechanisms of Development

• Publication date

  1999-05-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/S0925-4773(99)00024-6PMID 10507838
• 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.

• The STAR protein, GLD‐1, is a translational regulator of sexual identity in Caenorhabditis elegans

  1999cited by this paper
• Repression by the 3′ UTR of fem‐3, asex‐determining gene, relies on a ubiquitous mog‐dependent control in Caenorhabditis elegans

  1998cited by this paper
• Interactions between SRY and SOX genes in mammalian sex determination.

  1998influential reference
• Germ-line regulation of the Caenorhabditis elegans sex-determining gene tra-2.

  1998cited by this paper
• Sex-related genes, directional sexual selection, and speciation.

  1998cited by this paper
• Evidence for evolutionary conservation of sex-determining genes

  1998influential reference
• The murine fem1 gene family: homologs of the Caenorhabditis elegans sex-determination protein FEM-1.

  1998cited by this paper
• Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans

  1998cited by this paper
• The nuclear hormone receptor SEX-1 is an X-chromosome signal that determines nematode sex

  1998influential reference
• The evolutionary dynamics of sex determination.

  1998cited by this paper
• Molecular evolution of a sex determination protein. FEM-2 (pp2c) in Caenorhabditis.

  1998influential reference
• Dosage compensation in flies and worms: the ups and downs of X-chromosome regulation.

  1998cited by this paper
• Evolution of the Sry Genes

  1998cited by this paper
• Sex Determination and X Chromosome Dosage Compensation

  1997cited by this paper
• SDC-3 coordinates the assembly of a dosage compensation complex on the nematode X chromosome.

  1997cited by this paper
• Rapid evolution of sex-related genes in Chlamydomonas.

  1997cited by this paper
• Soma-germ cell interactions in Caenorhabditis elegans: multiple events of hermaphrodite germline development require the somatic sheath and spermathecal lineages.

  1997cited by this paper
• A conserved RNA-binding protein that regulates sexual fates in the C. elegans hermaphrodite germ line

  1997cited by this paper
• Evolution of the Sry genes.

  1997cited by this paper
• X-chromosome-counting mechanisms that determine nematode sex

  1997influential reference
• A genetic pathway for regulation of tra-2 translation.

  1997cited by this paper
• Conservation of the C.elegans tra‐2 3′UTR translational control

  1997cited by this paper
• A novel regulatory mutation in the C. elegans sex determination gene tra-2 defines a candidate ligand/receptor interaction site.

  1996influential reference
• Interspecies comparison reveals evolution of control regions in the nematode sex-determining gene tra-2.

  1996influential reference
• The tra‐3 sex determination gene of Caenorhabditis elegans encodes a member of the calpain regulatory protease family.

  1996cited by this paper
• Conservation of function and expression of unc-119 from two Caenorhabditis species despite divergence of non-coding DNA.

  1996cited by this paper
• Post-transcriptional regulation of sex determination in Caenorhabditis elegans: widespread expression of the sex-determining gene fem-1 in both sexes.

  1996cited by this paper
• Caenorhabditis elegans sex-determining protein FEM-2 is a protein phosphatase that promotes male development and interacts directly with FEM-3.

  1996influential reference
• Evolution of sex determination in caenorhabditis: unusually high divergence of tra-1 and its functional consequences.

  1996influential reference
• Dominant feminizing mutations implicate protein-protein interactions as the main mode of regulation of the nematode sex-determining gene tra-1.

  1995cited by this paper
• xol-1 acts as an early switch in the C. elegans male/hermaphrodite decision.

  1995cited by this paper
• gld-1, a tumor suppressor gene required for oocyte development in Caenorhabditis elegans.

  1995cited by this paper
• The origin and function of the mammalian Y chromosome and Y‐borne genes – an evolving understanding

  1995cited by this paper
• A predicted membrane protein, TRA-2A, directs hermaphrodite development in Caenorhabditis elegans.

  1995influential reference
• The fog-3 gene and regulation of cell fate in the germ line of Caenorhabditis elegans.

  1995influential reference
• Analysis of the multiple roles of gld-1 in germline development: interactions with the sex determination cascade and the glp-1 signaling pathway.

  1995cited by this paper
• The C. elegans sex-determining gene fem-2 encodes a putative protein phosphatase.

  1995influential reference
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  1994cited by this paper
• Identification of X chromosome regions in Caenorhabditis elegans that contain sex-determination signal elements.

  1994influential reference
• Identification of a candidate primary sex determination locus, fox-1, on the X chromosome of Caenorhabditis elegans.

  1994cited by this paper
• 2.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans

  1994cited by this paper
• Function of the her-1 gene is required for maintenance of male differentiation in adult tissues of C. elegans.

  1994cited by this paper
• Cloning by synteny: identifying C. briggsae homologues of C. elegans genes.

  1994cited by this paper
• Temperature sensitivity of sexual differentiation of gonads in the European pond turtle: Hormonal involvement

  1994cited by this paper
• Rapid sequence evolution of the mammalian sex-determining gene SRY

  1993cited by this paper
• The mog-1 gene is required for the switch from spermatogenesis to oogenesis in Caenorhabditis elegans.

  1993cited by this paper
• More mog genes that influence the switch from spermatogenesis to oogenesis in the hermaphrodite germ line of Caenorhabditis elegans.

  1993influential reference
• Feedback control of sex determination by dosage compensation revealed through Caenorhabditis elegans sdc-3 mutations.

  1993influential reference
• Independent domains of the Sdc-3 protein control sex determination and dosage compensation in C. elegans.

  1993cited by this paper
• Translational regulation of tra-2 by its 3' untranslated region controls sexual identity in C. elegans.

  1993cited by this paper
• Novel ubiquitin-like ribosomal protein fusion genes from the nematodes Caenorhabditis elegans and Caenorhabditis briggsae.

  1993cited by this paper
• Molecular characterization of the her-1 gene suggests a direct role in cell signaling during Caenorhabditis elegans sex determination.

  1993cited by this paper
• Rapid evolution of the sex determining locus in Old World mice and rats

  1993cited by this paper
• Zinc fingers in sex determination: only one of the two C. elegans Tra-1 proteins binds DNA in vitro.

  1993cited by this paper
• tra-2 encodes a membrane protein and may mediate cell communication in the Caenorhabditis elegans sex determination pathway.

  1992cited by this paper
• Interspecific comparison of the transformer gene of Drosophila reveals an unusually high degree of evolutionary divergence.

  1992cited by this paper
• Molecular genetics of sex determination in C. elegans.

  1992influential reference
• Molecular analysis of the C. elegans sex-determining gene tra-1: a gene encoding two zinc finger proteins.

  1992cited by this paper
• The Caenorhabditis elegans sex determining gene fem‐3 is regulated post‐transcriptionally.

  1992cited by this paper
• Early aspects of Caenorhabditis elegans sex determination and dosage compensation are regulated by a zinc-finger protein

  1991cited by this paper
• Molecular analysis of tra‐2, a sex determining gene in C.elegans.

  1991influential reference
• Sex-specific transcriptional regulation of the C. elegans sex-determining gene her-1.

  1991cited by this paper
• Control of the sperm–oocyte switch in Caenorhabditis elegans hermaphrodites by the fem-3 3′ untranslated region

  1991influential reference
• More is not better: brood size and population growth in a self-fertilizing nematode

  1991influential reference
• GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity

  1990cited by this paper
• Cloning and characterization of the segment polarity gene cubitus interruptus Dominant of Drosophila.

  1990influential reference
• The product of fem-1, a nematode sex-determining gene, contains a motif found in cell cycle control proteins and receptors for cell-cell interactions.

  1990cited by this paper
• The role of sdc-1 in the sex determination and dosage compensation decisions in Caenorhabditis elegans.

  1990cited by this paper
• Early C. elegans embryos are transcriptionally active.

  1990cited by this paper
• Observation of three new Sicuophoridae (Ciliophora, Clevellandellina) parasites of amphibians of Cameroon.

  1990cited by this paper
• fog-1, a regulatory gene required for specification of spermatogenesis in the germ line of Caenorhabditis elegans.

  1990influential reference
• Analysis of the role of tra-1 in germline sex determination in the nematode Caenorhabditis elegans.

  1989cited by this paper
• Drosophila doublesex gene controls somatic sexual differentiation by producing alternatively spliced mRNAs encoding related sex-specific polypeptides.

  1989cited by this paper
• The Caenorhabditis elegans gene sdc-2 controls sex determination and dosage compensation in XX animals.

  1989cited by this paper
• mab-3, a gene required for sex-specific yolk protein expression and a male-specific lineage in C. elegans.

  1988cited by this paper
• The GLI gene is a member of the Kruppel family of zinc finger proteins

  1988cited by this paper
• xol-1: a gene that controls the male modes of both sex determination and X chromosome dosage compensation in C. elegans.

  1988cited by this paper
• fog-2, a germ-line-specific sex determination gene required for hermaphrodite spermatogenesis in Caenorhabditis elegans.

  1988influential reference
• Molecular analysis of X chromosome dosage compensation in Caenorhabditis elegans.

  1987cited by this paper
• Primary sex determination in the nematode C. elegans.

  1987influential reference
• A genetic analysis of the sex-determining gene, tra-1, in the nematode Caenorhabditis elegans.

  1987influential reference
• Caenorhabditis elegans compensates for the difference in X chromosome dosage between the sexes by regulating transcript levels.

  1986cited by this paper
• Sex determination in the nematode C. elegans: analysis of tra-3 suppressors and characterization of fem genes.

  1986influential reference
• Activity of the sex-determining gene tra-2 is modulated to allow spermatogenesis in the C. elegans hermaphrodite.

  1986influential reference
• A sex-determining gene, fem-1, required for both male and hermaphrodite development in Caenorhabditis elegans.

  1984influential reference
• Specification of male development in Caenorhabditis elegans: the fem genes.

  1984influential reference
• More sex-determination mutants of Caenorhabditis elegans.

  1980influential reference
• Nondisjunction Mutants of the Nematode CAENORHABDITIS ELEGANS.

  1979influential reference
• Polyploids and sex determination in Caenorhabditis elegans.

  1979influential reference
• Fertilization and sperm competition in the nematode Caenorhabditis elegans.

  1979cited by this paper
• NONDISJUNCTION MUTANTS OF THE NEMATODE

  1979influential reference
• Intersex, a temperature-sensitive mutant of the nematode Caenorhabditis elegans.

  1978cited by this paper
• Post-embryonic cell lineages of the nematode, Caenorhabditis elegans.

  1977cited by this paper
• Mutations causing transformation of sexual phenotype in the nematode Caenorhabditis elegans.

  1977cited by this paper
• Synthesis of Ribonucleic Acid by the X-Chromosomes of Drosophila melanogaster and the Problem of Dosage Compensation

  1965cited by this paper
• Molecular Analysis

  1963cited by this paper

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