Literature DB >> 10477296

The Drosophila chiffon gene is required for chorion gene amplification, and is related to the yeast Dbf4 regulator of DNA replication and cell cycle.

G Landis1, J Tower.   

Abstract

The Drosophila chorion genes encode the major protein components of the chorion (eggshell) and are arranged in two clusters in the genome. To meet the demand for rapid chorion synthesis, Drosophila ovary follicle cells amplify the chorion gene clusters approximately 80-fold. Amplification proceeds through repeated firing of one or more DNA replication origins located near the center of each gene cluster. Hypomorphic mutant alleles of the chiffon gene cause thin, fragile chorions and female sterility, and were found to eliminate chorion gene amplification. Null alleles of chiffon had the additional phenotypes of rough eyes and thin thoracic bristles: phenotypes often associated with disruption of normal cell cycle. The chiffon locus was cloned by chromosomal walking from the nearby cactus locus. A 6.5 kb transcript was identified and confirmed to be chiffon by sequencing of mutant alleles and by phenotypic rescue with genomic transformation constructs. The protein predicted by translation of the 5.1 kb chiffon ORF contains two domains related to the S. cerevisiae Dbf4 regulator of DNA replication origin firing and cell cycle progression: a 44 residue domain designated CDDN1 (43% identical) and a 41 residue domain designated CDDN2 (12% identical). The CDDN domains were also found in the S. pombe homolog of Dbf4, Dfp1, as well as in the proteins predicted by translation of the Aspergillus nimO gene and specific human and mouse clones. The data suggest a family of eukaryotic proteins related to Dbf4 and involved in initiation of DNA replication.

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Year:  1999        PMID: 10477296     DOI: 10.1242/dev.126.19.4281

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  28 in total

1.  Functionally distinct, sequence-specific replicator and origin elements are required for Drosophila chorion gene amplification.

Authors:  L Lu; H Zhang; J Tower
Journal:  Genes Dev       Date:  2001-01-15       Impact factor: 11.361

2.  Selective instability of Orc1 protein accounts for the absence of functional origin recognition complexes during the M-G(1) transition in mammals.

Authors:  D A Natale; C J Li; W H Sun; M L DePamphilis
Journal:  EMBO J       Date:  2000-06-01       Impact factor: 11.598

3.  Schizosaccharomyces pombe Hsk1p is a potential cds1p target required for genome integrity.

Authors:  H A Snaith; G W Brown; S L Forsburg
Journal:  Mol Cell Biol       Date:  2000-11       Impact factor: 4.272

4.  Conservation of epigenetic regulation, ORC binding and developmental timing of DNA replication origins in the genus Drosophila.

Authors:  B R Calvi; B A Byrnes; A J Kolpakas
Journal:  Genetics       Date:  2007-11       Impact factor: 4.562

5.  Integrative analysis of gene amplification in Drosophila follicle cells: parameters of origin activation and repression.

Authors:  Jane C Kim; Jared Nordman; Fang Xie; Helena Kashevsky; Thomas Eng; Sharon Li; David M MacAlpine; Terry L Orr-Weaver
Journal:  Genes Dev       Date:  2011-07-01       Impact factor: 11.361

6.  Rapid DNA Synthesis During Early Drosophila Embryogenesis Is Sensitive to Maternal Humpty Dumpty Protein Function.

Authors:  Shera Lesly; Jennifer L Bandura; Brian R Calvi
Journal:  Genetics       Date:  2017-09-23       Impact factor: 4.562

7.  A mutation in Dbf4 motif M impairs interactions with DNA replication factors and confers increased resistance to genotoxic agents.

Authors:  Angela E Varrin; Ajai A Prasad; Rolf-Peter Scholz; Matthew D Ramer; Bernard P Duncker
Journal:  Mol Cell Biol       Date:  2005-09       Impact factor: 4.272

8.  Dm-myb mutant lethality in Drosophila is dependent upon mip130: positive and negative regulation of DNA replication.

Authors:  Eileen L Beall; Maren Bell; Daphne Georlette; Michael R Botchan
Journal:  Genes Dev       Date:  2004-07-15       Impact factor: 11.361

9.  An N-terminal domain of Dbf4p mediates interaction with both origin recognition complex (ORC) and Rad53p and can deregulate late origin firing.

Authors:  Bernard P Duncker; Kenji Shimada; Monika Tsai-Pflugfelder; Philippe Pasero; Susan M Gasser
Journal:  Proc Natl Acad Sci U S A       Date:  2002-11-19       Impact factor: 11.205

10.  A Dbf4p BRCA1 C-terminal-like domain required for the response to replication fork arrest in budding yeast.

Authors:  Carrie Gabrielse; Charles T Miller; Kristopher H McConnell; Aaron DeWard; Catherine A Fox; Michael Weinreich
Journal:  Genetics       Date:  2006-03-17       Impact factor: 4.562

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