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丙戊酸可增加脊髓性肌萎缩症(SMA)成纤维细胞系中SMN2的表达,并调节SF2/ASF和hnRNPA1的表达。

Valproic acid increases SMN2 expression and modulates SF2/ASF and hnRNPA1 expression in SMA fibroblast cell lines.

作者信息

Harahap Indra Sari Kusuma, Saito Toshio, San Lai Poh, Sasaki Naoko, Nurputra Dian Kesuma Pramudya, Yusoff Surini, Yamamoto Tomoto, Morikawa Satoru, Nishimura Noriyuki, Lee Myeong Jin, Takeshima Yasuhiro, Matsuo Masafumi, Nishio Hisahide

机构信息

Department of Community Medicine and Social Healthcare Science, Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

Brain Dev. 2012 Mar;34(3):213-22. doi: 10.1016/j.braindev.2011.04.010. Epub 2011 May 11.

Abstract

Spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular disorder that is caused by loss of the survival motor neuron gene, SMN1. SMA treatment strategies have focused on production of the SMN protein from the almost identical gene, SMN2. Valproic acid (VPA) is a histone deacetylase inhibitor that can increase SMN levels in some SMA cells or SMA patients through activation of SMN2 transcription or splicing correction of SMN2 exon 7. It remains to be clarified what concentration of VPA is required and by what mechanisms the SMN production from SMN2 is elicited. We observed that in two fibroblast cell lines from Japanese SMA patients, more than 1mM of VPA increased SMN2 expression at both the transcript and protein levels. VPA increased not only full-length (FL) transcript level but also exon 7-excluding (Δ7) transcript level in the cell lines and did not change the ratio of FL/Δ7, suggesting that SMN2 transcription was mainly activated. We also found that VPA modulated splicing factor expression: VPA increased the expression of splicing factor 2/alternative splicing factor (SF2/ASF) and decreased the expression of heterogeneous nuclear ribonucleoprotein A1 (hnRNPA1). In conclusion, more than 1mM of VPA activated SMN2 transcription and modulated the expression of splicing factors in our SMA fibroblast cell lines.

摘要

脊髓性肌萎缩症(SMA)是一种常见的常染色体隐性神经肌肉疾病,由存活运动神经元基因SMN1缺失引起。SMA的治疗策略集中在由几乎相同的基因SMN2产生SMN蛋白。丙戊酸(VPA)是一种组蛋白脱乙酰酶抑制剂,可通过激活SMN2转录或纠正SMN2外显子7的剪接,在一些SMA细胞或SMA患者中提高SMN水平。尚需阐明需要何种浓度的VPA以及通过何种机制引发由SMN2产生SMN。我们观察到,在来自日本SMA患者的两种成纤维细胞系中,超过1mM的VPA在转录本和蛋白水平上均增加了SMN2的表达。VPA不仅增加了细胞系中全长(FL)转录本水平,还增加了不含外显子7(Δ7)的转录本水平,且未改变FL/Δ7的比例,这表明SMN2转录主要被激活。我们还发现VPA调节剪接因子表达:VPA增加了剪接因子2/可变剪接因子(SF2/ASF)的表达,并降低了异质性核糖核蛋白A1(hnRNPA1)的表达。总之,超过l mM的VPA在我们的SMA成纤维细胞系中激活了SMN2转录并调节了剪接因子的表达。

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