相关实验视频
Updated: Feb 16, 2026

Antibody-Free Assay for RNA Methyltransferase Activity Analysis
Published on: July 9, 2019
通过驱逐CTCFF,Jpx RNA激活了Xist,从而激活了Xist
Sha Sun1, Brian C Del Rosario, Attila Szanto
1Howard Hughes Medical Institute, Department of Molecular Biology, Massachusetts General Hospital, and Department of Genetics, Harvard Medical School, Boston, MA 02114, USA.
X染色体不活化 (XCI) 是通过分子定位机制来调节的. JpxRNA与CTCF蛋白结合,将其从Xist基因中释放出来,在哺乳动物中启动XCI.
科学领域:
- 遗传学 是一个遗传学.
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 分子生物学分子生物学
背景情况:
- 哺乳动物的剂量补偿依赖于XX个体的X染色体失活 (XCI).
- 非编码的XistRNA启动XCI,但其精确的调节仍然不清楚.
- 现有的模型表明X-to-autosome比率 (X:A) 的依赖性,缺乏详细的分子见解.
研究的目的:
- 阐明控制XistRNA诱导和XCI启动的分子因素.
- 研究RNA和蛋白质在调节Xist转录中的相互作用.
- 了解CTCF在XCI监管中的作用机制.
主要方法:
- 研究了X编码RNA和自体编码蛋白之间的分子定位.
- 分析了CTCF蛋白在XCI前细胞中抑制Xist转录中的作用.
- 研究了JpxRNA上调对CTCF与Xist等位基因结合的影响.
主要成果:
- 证明JpxRNA,一个X编码的分子,在XCI开始时升级.
- 表明JpxRNA结合自体因子CTCF蛋白,并将其从Xist促进体释放出来.
- 已证实CTCF是一种由JpxRNA定位的RNA结合蛋白,从而激活Xist转录.
结论:
- 晶状体诱导是由JpxRNA和CTCF蛋白之间的分子定位决定的.
- 通过对抗CTCF介导的抑制,JpxRNA激活了Xist.
- 这种机制突显了长非编码RNAs在通过RNA-蛋白相互作用的表观遗传调节中的作用.
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12:42Quick Fluorescent In Situ Hybridization Protocol for Xist RNA Combined with Immunofluorescence of Histone Modification in X-chromosome Inactivation
Published on: November 26, 2014
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