The miti-mere and pdm1 genes collaborate during specification of the RP2/sib lineage in Drosophila neurogenesis

K. M. Bhat, S. J. Poole, P. Schedl

Research output: Contribution to journalArticle

49 Citations (Scopus)

Abstract

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 pdm1embryos 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.

Original languageEnglish (US)
Pages (from-to)4052-4063
Number of pages12
JournalMolecular and Cellular Biology
Volume15
Issue number8
StatePublished - 1995
Externally publishedYes

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Neurogenesis
Drosophila
Genes
Transgenes

ASJC Scopus subject areas

  • Cell Biology
  • Genetics
  • Molecular Biology

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The miti-mere and pdm1 genes collaborate during specification of the RP2/sib lineage in Drosophila neurogenesis. / Bhat, K. M.; Poole, S. J.; Schedl, P.

In: Molecular and Cellular Biology, Vol. 15, No. 8, 1995, p. 4052-4063.

Research output: Contribution to journalArticle

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