U bodies respond to nutrient stress in Drosophila

被引:22
作者
Buckingham, Mickey [1 ]
Liu, Ji-Long [1 ]
机构
[1] Univ Oxford, Dept Physiol Anat & Genet, MRC Funct Genom Unit, Oxford OX1 3QX, England
基金
英国医学研究理事会;
关键词
SMN; U body; P body; Nutrition stress; Drosophila; SPINAL MUSCULAR-ATROPHY; MOTOR-NEURON PROTEIN; MESSENGER-RNA; SMN COMPLEX; TRAILER HITCH; GENE-PRODUCT; SURVIVAL; GRANULES; IDENTIFICATION; LOCALIZATION;
D O I
10.1016/j.yexcr.2011.09.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The neurodegenerative disease spinal muscular atrophy (SMA) is caused by mutation of the survival motor neuron 1 (SMN1) gene. Cytoplasmic SMN protein-containing granules, known as U snRNP bodies (U bodies), are thought to be responsible for the assembly and storage of small nuclear ribonucleoproteins (snRNPs) which are essential for pre-mRNA splicing. U bodies exhibit close association with cytoplasmic processing bodies (P bodies), which are involved in mRNA decay and translational repression. The close association of the U body and P body in Drosophila resemble that of the stress granule and P body in yeast and mammalian cells. However, it is unknown whether the U body is responsive to any stress. Using Drosophila oogenesis as a model, here we show that U bodies increase in size following nutritional deprivation. Despite nutritional stress, U bodies maintain their close association with P bodies. Our results show that U bodies are responsive to nutrition changes, presumably through the U body-P body pathway. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:2835 / 2844
页数:10
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