Characterization of Ce-atl-1, an ATM-like gene from Caenorhabditis elegans

被引:21
作者
Aoki, H
Sato, S
Takanami, T
Ishihara, T
Katsura, I
Takahashi, H
Higashitani, A
机构
[1] Tohoku Univ, Inst Genet Ecol, Sendai, Miyagi 9808577, Japan
[2] Kazusa DNA Res Inst, Chiba 2920812, Japan
[3] Natl Inst Genet, Mishima, Shizuoka 4118540, Japan
来源
MOLECULAR AND GENERAL GENETICS | 2000年 / 264卷 / 1-2期
关键词
phosphoinositide kinases (PIKs); ataxia telangiectasia; checkpoint control; aneuploidy; RNAi;
D O I
10.1007/s004380000291
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
An ATM-like gene was identified in the genome of Caenorhabditis elegans. The putative product of the gene, termed Ce-atl-1 (C. elegans ATM-like 1) consists of 2514 amino acid residues. The C-terminal sequence, which contains a PI-3 kinase-like domain, showed good homology with the products of the gene MEC1/ESR1 from budding yeast, the rad3(+) gene of fission yeast and mammalian A TR (ataxia-telangiectasia and rad3(+) related) genes. The results of RNA-mediated interference indicated that the major phenotype associated with repression of Ce-atl-1 was lethality (approximately 50-80%) during early embryogenesis. Among the surviving progeny, males (XO animals) arose at a high frequency (2-30%). In addition, 5% of oocyte chromosomes demonstrated aneuploidy due to a defect in pre-meiotic chromosomal segregation. Gene expression analyses indicated that Ce-atl-1 mRNA was expressed in all larval stages and that its level increased about fivefold in the adult stage. The adult expression level was de creased in the glp-4 mutant, which is defective in germ line proliferation. Ce-atl-1 was strongly expressed in both the mitotic and meiotic cells of adult gonads. In summary, Ce-atl-1 appears to be important for early embryogenesis, and loss of its function results in a defect in chromosome segregation, similar to what has been observed for AT-related proteins.
引用
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页码:119 / 126
页数:8
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