HORKA, A DOMINANT MUTATION OF DROSOPHILA, INDUCES NONDISJUNCTION AND,THROUGH PATERNAL EFFECT, CHROMOSOME LOSS AND GENETIC MOSAICS

Citation
J. Szabad et al., HORKA, A DOMINANT MUTATION OF DROSOPHILA, INDUCES NONDISJUNCTION AND,THROUGH PATERNAL EFFECT, CHROMOSOME LOSS AND GENETIC MOSAICS, Genetics, 139(4), 1995, pp. 1585-1599
Citations number
54
Categorie Soggetti
Genetics & Heredity
Journal title
ISSN journal
00166731
Volume
139
Issue
4
Year of publication
1995
Pages
1585 - 1599
Database
ISI
SICI code
0016-6731(1995)139:4<1585:HADMOD>2.0.ZU;2-H
Abstract
Fs(3)Horka (Horka) was described as a dominant female-sterile mutation of Drosophila melanogaster. Genetic and cytological data show that Ho rka induces mostly equational nondisjunction during spermatogenesis bu t not chromosome loss and possesses a dominant paternal effect: the X, second, third and the fourth chromosomes, but not the Y, are rendered unstable while undergoing spermatogenesis and may be lost in the desc ending zygotes. The frequency of Horka-induced chromosome loss is usua lly 2-4% but varies with the genetic background and can be over 20%. T he X chromosome loss occurs during the gonomeric and the initial cleav age divisions. Loss of the X and fourth chromosomes shows no correlati on. We propose, based on similarities in the mutant phenotypes with th e chromosome destabilizing mutations nonclaret disjunctional and pater nal loss, that the normal Horka(+) product is required for function of the centromeres and/or nearby regions. Horka is a convenient tool for the generation of gynandromorphs, autosome mosaics and for the study of gene expression in mosaics.