A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

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Citation Lin, H.C., Wu, J.T., Tan, B.C., Chien, C.T. (2009). Cul4 and DDB1 regulate Orc2 localization, BrdU incorporation and Dup stability during gene amplification in Drosophila follicle cells.  J. Cell Sci. 122(14): 2393--2401. (Export to RIS)
FlyBase ID FBrf0208137
Publication Type Research paper
PubMed ID 19531585
PubMed Abstract In higher eukaryotes, the pre-replication complex (pre-RC) component Cdt1 is the major regulator in licensing control for DNA replication. The Cul4-DDB1-based ubiquitin ligase mediates Cdt1 ubiquitylation for subsequent proteolysis. During the initiation of chorion gene amplification, Double-parked (Dup), the Drosophila ortholog of Cdt1, is restricted to chorion gene foci. We found that Dup accumulated in nuclei in Cul4 mutant follicle cells, and the accumulation was less prominent in DDB1 mutant cells. Loss of Cul4 or DDB1 activity in follicle cells also compromised chorion gene amplification and induced ectopic genomic DNA replication. The focal localization of Orc2, a subunit of the origin recognition complex, is frequently absent in Cul4 mutant follicle cells. Therefore, Cul4 and DDB1 have differential functions during chorion gene amplification.
DOI 10.1242/jcs.042861
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Language of Publication English
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Publication Type Journal
Abbreviation J. Cell Sci.
Title Journal of Cell Science
Publication Year 1966-
ISBN/ISSN 0021-9533
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