Affiliation:
1. Laboratoire de Génétique et Physiologie du Développement, UMR 6545 CNRS-Université, IBDM CNRS-INSERM-Université de la Méditerrannée, F-13288 Marseille Cedex 09, France
Abstract
ABSTRACT
We have characterized the
Drosophila bancal
gene, which encodes a
Drosophila
homologue of the vertebrate hnRNP K protein. The
bancal
gene is essential for the correct size of adult appendages. Reduction of appendage size in
bancal
mutant flies appears to be due mainly to a reduction in the number of cell divisions in the imaginal discs. Transgenes expressing
Drosophila
or human hnRNP K are able to rescue weak
bancal
phenotype, showing the functional similarity of these proteins in vivo. High levels of either human or
Drosophila
hnRNP K protein in imaginal discs induces programmed cell death. Expression of the antiapoptotic P35 protein suppresses this phenotype in the eye, suggesting that apoptosis is the major cellular defect caused by overexpression of K protein. Finally, the human K protein acts as a negative regulator of
bancal
gene expression. We propose that negative autoregulation limits the level of Bancal protein produced in vivo.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
36 articles.
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