humpty dumpty is required for developmental DNA amplification and cell proliferation in Drosophila

被引:30
作者
Bandura, JL
Beall, EL
Bell, M
Silver, HR
Botchan, MR
Calvi, BR [1 ]
机构
[1] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.cub.2005.02.063
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The full complement of proteins required for the proper regulation of genome duplication are yet to be described. We employ a genetic DNA-replication model system based on developmental amplification of Drosophila eggshell (chorion) genes [1]. Hypomorphic mutations in essential DNA replication genes result in a distinct thin-eggshell phenotype owing to reduced amplification [2]. Here, we molecularly identify the gene, which we have named humpty dumpty (hd), corresponding to the thin-eggshell mutant fs(3)272-9 [3]. We confirm that hd is essential for DNA amplification in the ovary and show that it also is required for cell proliferation during development. Mosaic analysis of hd mutant cells during development and RNAi in Kc cells reveal that depletion of Hd protein results in severe defects in genomic replication and DNA damage. Most Hd protein is found in nuclear foci, and some may traverse the nuclear envelope. Consistent with a role in DNA replication, expression of Hd protein peaks during late G1 and S phase, and it responds to the E2F1/Dp transcription factor. Hd protein sequence is conserved from plants to humans, and published microarrays indicate that expression of its putative human ortholog also peaks at G1/S [4]. Our data suggest that hd defines a new gene family likely required for cell proliferation in all multicellular eukaryotes.
引用
收藏
页码:755 / 759
页数:5
相关论文
共 21 条
[1]   Protein repeats: Structures, functions, and evolution [J].
Andrade, MA ;
Perez-Iratxeta, C ;
Ponting, CP .
JOURNAL OF STRUCTURAL BIOLOGY, 2001, 134 (2-3) :117-131
[2]   Ectopic E2F expression induces S phase and apoptosis in Drosophila imaginal discs [J].
Asano, M ;
Nevins, JR ;
Wharton, RP .
GENES & DEVELOPMENT, 1996, 10 (11) :1422-1432
[3]   Chorion gene amplification in Drosophila:: A model for metazoan origins of DNA replication and S-phase control [J].
Calvi, BR ;
Spradling, AC .
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1999, 18 (03) :407-417
[4]   Cell cycle control of chorion gene amplification [J].
Calvi, BR ;
Lilly, MA ;
Spradling, AC .
GENES & DEVELOPMENT, 1998, 12 (05) :734-744
[5]   The nuclear location and chromatin organization of active chorion amplification origins [J].
Calvi, BR ;
Spradling, AC .
CHROMOSOMA, 2001, 110 (03) :159-172
[6]  
CARPENTER ATC, 1999, DROS INF SERV, V82, P113
[7]   Redundancy, insult-specific sensors and thresholds: unlocking the S-phase checkpoint response [J].
Cobb, JA ;
Shimada, K ;
Gasser, SM .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2004, 14 (03) :292-300
[8]   Cell cycle-dependent and cell cycle-independent control of transcription by Drosophila E2F/RB pathway [J].
Dimova, DK ;
Stevaux, O ;
Frolov, MV ;
Dyson, NJ .
GENES & DEVELOPMENT, 2003, 17 (18) :2308-2320
[9]   FlyBase: genes and gene models [J].
Drysdale, RA ;
Crosby, MA .
NUCLEIC ACIDS RESEARCH, 2005, 33 :D390-D395
[10]   Control of growth and organ size in Drosophila [J].
Johnston, LA ;
Gallant, P .
BIOESSAYS, 2002, 24 (01) :54-64