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Condensation properties of stress granules and processing bodies are compromised in myotonic dystrophy type 1
被引:2
|作者:
Gulyurtlu, Selma
[1
]
Magon, Monika S.
[1
]
Guest, Patrick
[1
]
Papavasiliou, Panagiotis P.
[1
]
Morrison, Kim D.
[1
]
Prescott, Alan R.
[2
]
Sleeman, Judith E.
[1
]
机构:
[1] Univ St Andrews, Sch Biol, Biomol Sci Res Complex, St Andrews KY16 9ST, Fife, Scotland
[2] Univ Dundee, Sch Life Sci, Div Cell Signalling & Immunol, Dundee DD1 5EH, Scotland
基金:
英国惠康基金;
美国安德鲁·梅隆基金会;
英国生物技术与生命科学研究理事会;
关键词:
LLPS;
Myotonic dystrophy type 1;
P-bodies;
Stress granules;
Trinucleotide repeats;
MESSENGER-RNA;
BINDING PROTEIN;
OXIDATIVE STRESS;
CAJAL BODY;
TOXIC RNA;
LOCALIZATION;
TRANSLATION;
AUTOPHAGY;
CUGBP1;
MODEL;
D O I:
10.1242/dmm.049294
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
RNA regulation in mammalian cells requires complex physical compartmentalisation, using structures thought to be formed by liquid-liquid phase separation. Disruption of these structures is implicated in numerous degenerative diseases. Myotonic dystrophy type 1 (DM1) is a multi-systemic trinucleotide repeat disorder resulting from an expansion of nucleotides CTG (CTGexp) in the DNA encoding DM1 protein kinase (DMPK). The cellular hallmark of DM1 is the formation of nuclear foci that contain expanded DMPK RNA (CUGexp) (with thymine instead of uracil). We report here the deregulation of stress granules (SGs) and processing bodies (P-bodies), two cytoplasmic structures key for mRNA regulation, in cell culture models of DM1. Alterations to the rates of formation and dispersal of SGs suggest an altered ability of cells to respond to stress associated with DM1, while changes to the structure and dynamics of SGs and P-bodies suggest that a widespread alteration to the biophysical properties of cellular structures is a consequence of the presence of CUGexp RNA.
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页数:18
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