Abstract
In the nematode Caenorhabditis elegans, hermaphrodite recombination has been characterized and is the basis of the genetic map used in this organism. In this study we have examined male recombination on linkage group I and have found it to be approximately one-third less than that observed in the hermaphrodite. This decrease was interval-dependent and nonuniform. We observed less recombination in the male in 5 out of 6 intervals examined, and no observable difference in one interval on the right end of LG I. Hermaphrodite recombination frequencies are the result of recombination in two germlines; oocyte and hermaphrodite spermatocytes. We have measured recombination in the oocyte and have found it to be approximately twofold lower than that calculated for hermaphrodite spermatocytes and not significantly different from the male spermatocyte frequency. Thus, recombination frequencies appear to be a function of gonad physiology rather than the sex of the germline. Evidence from experiments examining the effect of karyotype on recombination in males sexually transformed by the her-1 mutation into XO hermaphrodites (normally XX), suggests the sexual phenotype rather than genotype determines the recombination frequency characteristic of a particular sex. Hermaphrodite recombination is known to be affected by temperature, maternal age, and the rec-1 mutation. We have examined the effect of these parameters on recombination in the male and have found male recombination frequency increased with elevated temperatures and in the presence of Rec-1, and decreased with paternal age.
MeSH Terms
Animals
Caenorhabditis/genetics
Crossing Over, Genetic
Disorders of Sex Development/genetics
Exodeoxyribonuclease V
Female
Fungal Proteins/genetics
Genetic Linkage
Genotype
Karyotyping
Male
Mutation
Oocytes/metabolism
Phenotype
Sex Characteristics
Spermatocytes/metabolism
Temperature
Chemicals
Fungal Proteins
Exodeoxyribonuclease V
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Zetka M C
Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
Rose A M
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