Snipper, an Eri1 homologue, affects histone mRNA abundance and is crucial for normal Drosophila melanogaster development

被引:4
作者
Alexiadis, Anastasios [1 ,2 ]
Delidakis, Christos [1 ,2 ]
Kalantidis, Kriton [1 ,2 ]
机构
[1] Fdn Res & Technol Hellas, Inst Mol Biol & Biotechnol, N Plastira 100, Iraklion 70013, Greece
[2] Univ Crete, Dept Biol, Iraklion, Greece
来源
FEBS LETTERS | 2017年 / 591卷 / 14期
关键词
exonuclease; histone mRNA processing; larval arrest; LOOP BINDING-PROTEIN; 5.8S RIBOSOMAL-RNA; CELL-CYCLE PROGRESSION; STEM-LOOP; C-ELEGANS; 3' END; CAENORHABDITIS-ELEGANS; GENE-EXPRESSION; IN-VIVO; DEGRADATION;
D O I
10.1002/1873-3468.12719
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 conserved 3'-5' RNA exonuclease ERI1 is implicated in RNA interference inhibition, 5.8S rRNA maturation and histone mRNA maturation and turnover. The single ERI1 homologue in Drosophila melanogaster Snipper (Snp) is a 3'-5' exonuclease, but its in vivo function remains elusive. Here, we report Snp requirement for normal Drosophila development, since its perturbation leads to larval arrest and tissue-specific downregulation results in abnormal tissue development. Additionally, Snp directly interacts with histone mRNA, and its depletion results in drastic reduction in histone transcript levels. We propose that Snp protects the 30-ends of histone mRNAs and upon its absence, histone transcripts are readily degraded. This in turn may lead to cell cycle delay or arrest, causing growth arrest and developmental perturbations.
引用
收藏
页码:2106 / 2120
页数:15
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