Molecular Human Reproduction, Vol 3, 853-862, Copyright © 1997 by Oxford University Press
WM Deng, D Zhao, K Rothwell and M Bownes
We report the analysis of a number of lines of Drosophila melanogaster
containing insertions of the yeast gal4 gene. By crossing a UAS-lacZ fusion
gene as a reporter into these lines, we analysed the expression patterns of
beta-galactosidase during oogenesis. Since there is no expression of GAL4
in the germ-line in these experiments, this is an ideal system for the
analysis of expression patterns in sub-sets of follicle cells. These lines
provide ideal markers for sets of follicle cells, e.g. anterior or
posterior polar cells for studying genetic interactions in oogenesis;
however, they can also be used in the same way as conventional enhancer
traps to clone nearby genes with similar expression patterns. The
advantages of this dual gal4/UAS system over conventional enhancer trapping
includes the possibility of GAL4- directed misexpression and antisense
expression studies to establish the function of the genes we identified
during follicle cell determination and differentiation. These studies could
lead to the isolation of homologous genes crucial in mammalian oogenesis.
Understanding how the somatic cells and germ cells interact to promote
growth and maturation of the mammalian follicle and oocyte could well be
crucial for improving the fertility of eggs used for in-vitro fertilization
programmes, and could provide methods for assessing the quality of eggs.
JOURNAL ARTICLE
Analysis of P[gal4] insertion lines of Drosophila melanogaster as a route to identifying genes important in the follicle cells during oogenesis
Institute of Cell and Molecular Biology, University of Edinburgh, UK.
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