VA Boston Healthcare System, MA, USA.
Cell Death Differ. 2011 Nov;18(11):1726-35. doi: 10.1038/cdd.2011.38. Epub 2011 May 6.
Huntington's disease (HD) is an autosomal-dominant neurological disorder caused by expanded CAG repeats in the Huntingtin (Htt) gene, but it is not known how this mutation causes neurodegeneration. Herein, we found that dysfunction of upstream binding factor-1 (UBF-1) is linked to reduced ribosomal DNA (rDNA) transcription in HD. We identified that UBF1 acetylation at Lys (K) 352 by CREB binding protein (CBP) is crucial for the transcriptional activity of rDNA. UBF1 mutation (K352A, K352Q, and K352R) decreased rDNA transcriptional activity. Moreover, both CBP-dHAT mutant and knockdown of CBP by siRNA reduced acetylation of UBF1 and resulted in the decreased transcription of rDNA into rRNA. ChIP analysis showed a significant reduction of UBF1 occupancy in the promoter of rDNA in STHdh(Q111) cell line model of HD. These results demonstrate that abnormal activity of UBF1 and its acetylation by CBP are linked to impaired rDNA transcription in HD. This novel mechanism suggests that modulation of UBF-mediated rDNA synthesis by CBP may be a therapeutic target for improving neuronal rDNA transcription in HD.
亨廷顿病 (HD) 是一种常染色体显性遗传的神经退行性疾病,由亨廷顿 (Htt) 基因中 CAG 重复序列的扩展引起,但尚不清楚这种突变如何导致神经退行性变。在此,我们发现上游结合因子-1 (UBF-1) 的功能障碍与 HD 中核糖体 DNA (rDNA) 转录减少有关。我们发现 CREB 结合蛋白 (CBP) 对 UBF1 赖氨酸 (K) 352 的乙酰化对于 rDNA 的转录活性至关重要。UBF1 突变 (K352A、K352Q 和 K352R) 降低了 rDNA 的转录活性。此外,CBP-dHAT 突变体和 siRNA 敲低 CBP 均降低了 UBF1 的乙酰化,导致 rDNA 转录成 rRNA 的减少。ChIP 分析显示,在 HD 的 STHdh(Q111) 细胞系模型中,rDNA 启动子处 UBF1 的占有率显著降低。这些结果表明,UBF1 的异常活性及其被 CBP 乙酰化与 HD 中 rDNA 转录受损有关。这一新机制表明,通过 CBP 调节 UBF 介导的 rDNA 合成可能是改善 HD 中神经元 rDNA 转录的治疗靶点。