AtPARN is an essential poly(A) ribonuclease in Arabidopsis

被引:56
作者
Chiba, Y
Johnson, MA
Lidder, P
Vogel, JT
van Erp, H
Green, PJ [1 ]
机构
[1] Univ Delaware, Delaware Biotechnol Inst, Dept Plant & Soil Sci, Newark, DE 19711 USA
[2] Univ Chicago, Dept Mol Genet & Cell Biol, Chicago, IL 60637 USA
[3] Michigan State Univ, Dept Energy Plant Res Lab, E Lansing, MI 48824 USA
基金
美国国家科学基金会; 日本学术振兴会;
关键词
deadenylation; mRNA turnover; poly(A) degradation; mRNA stability;
D O I
10.1016/j.gene.2003.11.028
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Deadenylation is the first and rate-limiting step in the degradation of many mRNAs in a wide-range of organisms from yeast to higher eukaryotes. It can also play a regulatory role in early development. In this study, we examined the Arabidopsis homolog of poly(A) ribonuclease (PARN), a deadenylase first identified in mammals and absent from yeast. Consistent with the conservation of domains and residues important for catalytic activity, Arabidopsis PARN (AtPARN) expressed in Escherichia coli has poly(A) degradation activity in vitro. Protein localization experiments in plant cells indicate that AtPARN resides in both the nucleus and cytoplasm. To address the importance of the enzyme in vivo, we identified three independent T-DNA insertion mutants of AtRARN which interrupt the gene at different positions between the ATG and the stop codon. All three alleles cause lethality prior to seed germination, indicating that AtRARN is an essential gene first required during early development. Although homologous genes have yet to be inactivated in any other organism, our observations argue for the critical importance of PARN and suggest that it may be essential in many other multicellular eukaryotes. (C) 2004 Elsevier B.V. All rights reserved.
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页码:95 / 102
页数:8
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