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Polyglutamine-expanded ataxin-7 inhibits STAGA histone acetyltransferase activity to produce retinal degeneration
被引:187
作者:
Palhan, VB
Chen, SM
Peng, GH
Tjernberg, A
Gamper, AM
Fan, YX
Chait, BT
La Spada, AR
Roeder, RG
机构:
[1] Rockefeller Univ, Biochem & Mol Biol Lab, New York, NY 10021 USA
[2] Rockefeller Univ, Lab Mass Spectrometry & Gaseous Ion Chem, New York, NY 10021 USA
[3] Washington Univ, Sch Med, Dept Ophthalmol & Visual Sci, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[5] Univ Washington, Med Ctr, Dept Lab Med, Seattle, WA 98195 USA
[6] Univ Washington, Med Ctr, Dept Med, Div Med Genet, Seattle, WA 98195 USA
[7] Univ Washington, Med Ctr, Dept Neurol, Div Neurogenet, Seattle, WA 98195 USA
[8] Univ Washington, Med Ctr, Ctr Neurogenet & Neurotherapeut, Seattle, WA 98195 USA
来源:
关键词:
SCA7;
transcription;
neurodegeneration;
poly(Q);
CRX;
D O I:
10.1073/pnas.0503505102
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Spinocerebellar ataxia type 7 (SCA7) is characterized by cone-rod dystrophy retinal degeneration and is caused by a polyglutamine [poly(Q)] expansion within ataxin-7, a protein of previously unknown function. Here, we report that ataxin-7 is an integral component of the mammalian STAGA (SPT3-TAF9-ADA-GCN5 acetyltransferase) transcription coactivator complex, interacts directly with the GCN5 histone acetyltransferase component of STAGA, and mediates a direct interaction of STAGA with the CRX (cone-rod homeobox) transactivator of photoreceptor genes. Consistent with these results, chromatin immunoprecipitation assays document retinal-specific association of CRX, GCN5, and acetylated histone H3 with CRX target genes. RNA interference studies also implicate ataxin-7 and GCN5 in CRX-dependent gene activation, and histone deacetylase inhibitors restore the compromised expression of a CRX target gene in an ataxin-7-deficient background. Significantly, in relation to SCA7, poly(Q)-expanded ataxin-7 gets incorporated into STAGA and, in a dominant-negative manner, inhibits the nucleosomal histone acetylation function of STAGA GCN5 both in vitro and, based on chromatin immunoprecipitation assays, in SCA7 transgenic mice. These results suggest that the normal function of a poly(Q) disease protein may intersect with its pathogenic mechanism, an observation with significant implications for the molecular basis of all poly(Q) disorders and ultimately for their treatment.
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页码:8472 / 8477
页数:6
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