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A method for studying tissue specificity of maternally affected Drosophila melanogaster mutants: mosaic analysis of cinnamon.
Authors:M Nissani  K Fellinger
Affiliation:1. School of Biological Sciences, The Flinders University, Bedford Park, South Australia 5042 Australia;2. Department of Genetics, University of Wisconsin, Madison, Wisconsin 53706 USA
Abstract:Mosaic analysis is introduced to study tissue specificity of the maternal effect which characterizes the wild-type allele of cinnamon (=cin). The methodology presented is applicable to studies of other maternal effect mutations, as well as to female or male sterility mutations. One hundred and forty-three pal-induced fertile cin-mosaic females were obtained, and the degree to which they were capable of maternally affecting their homozygous cin daughters was correlated to their cuticular and germinal genetic constitution. From this analysis the following conclusions are drawn: (1) The presence of a wild-type (cin+) allele in maternal germ cells constitutes a sufficient condition for the full expression of the cin+ characteristic maternal effect: All cin offspring derived from such cells have normal viability and eye color. (2) This effect is confined to the descendants of a particular germ cell and does not extend to the descendants of other non-cin+ germ cells in the same or in a neighboring ovary. (3) A wild-type allele in a germ cell constitutes a necessary condition for the eye color maternal effect. (4) When a maternal germ line is wholly mutant, nonmutant constitution of an additional focus may result in rescue of more than half of the homozygous cin offspring (all with mutant eye color). Mosaic analysis suggests that this somatic viability focus originates from the posterior region of the blastoderm. These conclusions were tested and confirmed by transplanting heterozygous cin ovaries, wild-type Malphigian tubes, and wild-type fat body into homozygous cin hosts. In addition, transplantations of homozygous cin ovaries into wild-type hosts suggest that the posterior maternal viability focus corresponds to the mesodermal components of the ovaries.
Keywords:Send reprint requests to: M. Nissani   Center for Pathobiology   University of California   Irvine   California 92717.
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