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PMID: 3557107 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Gain-of-function mutations of fem-3, a sex-determination gene in Caenorhabditis elegans.

Genetics ·Vol. 115 ·No. 1 ·1987-01-00 ·Pages 107-19

Barton MK, Schedl TB, Kimble J

Abstract

We have isolated nine gain-of-function (gf) alleles of the sex-determination gene fem-3 as suppressors of feminizing mutations in fem-1 and fem-2. The wild-type fem-3 gene is needed for spermatogenesis in XX self-fertilizing hermaphrodites and for male development in both soma and germ line of XO animals. Loss-of-function alleles of fem-3 transform XX and XO animals into females (spermless hermaphrodites). In contrast, fem-3(gf) alleles masculinize only one tissue, the hermaphrodite germ line. Thus, XX fem-3(gf) mutant animals have a normal hermaphrodite soma, but the germ line produces a vast excess of sperm and no oocytes. All nine fem-3(gf) alleles are temperature sensitive. The temperature-sensitive period is from late L4 to early adult, a period just preceding the first signs of oogenesis. The finding of gain-of-function alleles which confer a phenotype opposite to that of loss-of-function alleles supports the idea that fem-3 plays a critical role in germ-line sex determination. Furthermore, the germ-line specificity of the fem-3(gf) mutant phenotype and the late temperature-sensitive period suggest that, in the wild-type XX hermaphrodite, fem-3 is negatively regulated so that the hermaphrodite stops making sperm and starts making oocytes. Temperature shift experiments also show that, in the germ line, sexual commitment appears to be a continuing process. Spermatogenesis can resume even after oogenesis has begun, and oogenesis can be initiated much later than normal.

MeSH Terms
Alleles Animals Caenorhabditis/genetics,growth & development Disorders of Sex Development Female Genes, Regulator Male Mutation Phenotype Sex Determination Analysis Suppression, Genetic Temperature
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Barton M K
Schedl T B
Kimble J
References (33)
33 references, click to expand
  1. Dual role for Escherichia coli RecA protein in SOS mutagenesis.
    Proc Natl Acad Sci U S A. 1985 May;82(10):3325-9 PMID: 3159017
  2. Mutant single-strand binding protein of Escherichia coli: genetic and physiological characterization.
    J Bacteriol. 1979 Oct;140(1):14-9 PMID: 227832
  3. Coupling with packaging explains apparent nonreciprocality of Chi-stimulated recombination of bacteriophage lambda by RecA and RecBC functions.
    Genetics. 1984 Dec;108(4):773-94 PMID: 6239809
  4. Escherichia coli RecBC pseudorevertants lacking chi recombinational hotspot activity.
    J Bacteriol. 1983 Aug;155(2):664-80 PMID: 6348024
  5. Mutations causing transformation of sexual phenotype in the nematode Caenorhabditis elegans.
    Genetics. 1977 Jun;86(2 Pt. 1):275-87 PMID: 560330
  6. The SOS regulatory system of Escherichia coli.
    Cell. 1982 May;29(1):11-22 PMID: 7049397
  7. The genetics of Caenorhabditis elegans.
    Genetics. 1974 May;77(1):71-94 PMID: 4366476
  8. recD: the gene for an essential third subunit of exonuclease V.
    Proc Natl Acad Sci U S A. 1986 Aug;83(15):5558-62 PMID: 3526335
  9. Miscellaneous: In praise of the Basuto pony.
    Br Med J (Clin Res Ed). 1983 Dec 24;287(6409):1985-7 PMID: 20742150
  10. Directionality and nonreciprocality of Chi-stimulated recombination in phage lambda.
    Genetics. 1980 Feb;94(2):235-48 PMID: 6446478
  11. A uniform genetic nomenclature for the nematode Caenorhabditis elegans.
    Mol Gen Genet. 1979 Sep;175(2):129-33 PMID: 292825
  12. Reciprocal and non-reciprocal recombination in bacteriopahge lambda.
    J Mol Biol. 1969 Jul 28;43(2):351-5 PMID: 5804921
  13. A new class of Escherichia coli recBC mutants: implications for the role of RecBC enzyme in homologous recombination.
    Proc Natl Acad Sci U S A. 1984 Dec;81(24):7850-4 PMID: 6393130
  14. Chi-dependent DNA strand cleavage by RecBC enzyme.
    Cell. 1985 May;41(1):145-51 PMID: 3888404
  15. Escherichia coli mutants with temperature-sensitive synthesis of DNA.
    Mol Gen Genet. 1970;109(2):107-22 PMID: 4925091
  16. Unusual alleles of recB and recC stimulate excision of inverted repeat transposons Tn10 and Tn5.
    Proc Natl Acad Sci U S A. 1984 Feb;81(3):824-8 PMID: 6322169
  17. Novobiocin and coumermycin inhibit DNA supercoiling catalyzed by DNA gyrase.
    Proc Natl Acad Sci U S A. 1976 Dec;73(12):4474-8 PMID: 794878
  18. A role for recombination in the production of "free-loader" lambda bacteriophage particles.
    J Mol Biol. 1972 Jul 14;68(1):57-67 PMID: 4559113
  19. Purified Escherichia coli recA protein catalyzes homologous pairing of superhelical DNA and single-stranded fragments.
    Proc Natl Acad Sci U S A. 1979 Apr;76(4):1638-42 PMID: 156361
  20. Genetics and function of DNA ligase in Escherichia coli.
    J Mol Biol. 1973 Jul 15;77(4):531-47 PMID: 4353284
  21. Orientation of cohesive end site cos determines the active orientation of chi sequence in stimulating recA . recBC-mediated recombination in phage lambda lytic infections.
    Proc Natl Acad Sci U S A. 1982 Oct;79(19):5981-5 PMID: 6310557
  22. Temperature-sensitive developmental mutants of Caenorhabditis elegans.
    Dev Biol. 1976 Mar;49(1):220-35 PMID: 943345
  23. Rec-mediated recombinational hot spot activity in bacteriophage lambda. II. A mutation which causes hot spot activity.
    Genetics. 1974 Jul;77(3):425-33 PMID: 4415485
  24. LambdaattB-attP, a lambda derivative containing both sites involved in integrative recombination.
    Virology. 1974 Jan;57(1):207-16 PMID: 4206535
  25. recA-dependent genetic switch generated by transposon Tn10.
    J Mol Biol. 1980 Dec 5;144(2):215-21 PMID: 6262517
  26. Localized Negative Interference in Bacteriophage.
    Genetics. 1965 Mar;51(3):369-79 PMID: 17248239
  27. Cotransduction with thy of a gene required for genetic recombination in Escherichia coli.
    J Bacteriol. 1967 May;93(5):1729-31 PMID: 5337851
  28. DNA topoisomerases.
    Annu Rev Biochem. 1981;50:879-910 PMID: 6267993
  29. RecBC enzyme nicking at Chi sites during DNA unwinding: location and orientation-dependence of the cutting.
    Cell. 1985 May;41(1):153-63 PMID: 3888405
  30. Conditional-lethal mutations that suppress genetic defects in morphogenesis by altering structural proteins.
    Proc Natl Acad Sci U S A. 1975 Jul;72(7):2738-42 PMID: 1101263
  31. Suppression of an amber mutation by microinjection of suppressor tRNA in C. elegans.
    Nature. 1982 Sep 30;299(5882):456-8 PMID: 7121584
  32. Bacteriophage lambda; abortive infection of bacteria lysogenic for phage P2.
    Proc Natl Acad Sci U S A. 1970 Jul;66(3):587-94 PMID: 4913204
  33. Single burst study of rec- and red-mediated recombination in bacteriophage lambda.
    Proc Natl Acad Sci U S A. 1976 Dec;73(12):4613-7 PMID: 1070013
Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
0016-6731
Published
1987-01-00
Pages
107-19
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC1203045
Subset
IM
Grants
NIGMS NIH HHS · GM09554 · United States
NIGMS NIH HHS · GM31816 · United States
NICHD NIH HHS · HD00630 · United States
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