Previous Article | Next Article ![]()
Mol. Cell. Biol., Aug 1995, 4052-4063, Vol 15, No. 8
KM Bhat, SJ Poole and P Schedl
We have investigated (i) the role of pdm1, a Drosophila POU gene, during
the elaboration of the GMC-1-->RP2/sib lineage and (ii) the functional
relationship between pdm1 and the closely linked second POU gene,
miti-mere, in this lineage. We show that deletion of pdm1 causes a
partially penetrant GMC-1 defect, while deletion of both miti and pdm1
results in a fully penetrant defect. This GMC-1 defect in miti- and pdm1-
embryos can be rescued by the pdm1 or miti transgene. Rescue is observed
only when these genes are expressed at the time of GMC-1 formation.
Overexpression of pdm1 or miti well after GMC-1 is formed results in the
duplication of RP2 and/or sib cells. Our results indicate that both genes
are required for the normal development of this lineage and that the two
collaborate during the specification of GMC-1 identity.
Copyright © 1995, American Society for Microbiology
The miti-mere and pdm1 genes collaborate during specification of the RP2/sib lineage in Drosophila neurogenesis
Department of Molecular Biology, Princeton University, New Jersey 08544, USA.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»