序列和源代基因依赖的m6A对等位基因特异性基因表达有所贡献
Ying Zhang1,2,3, Ze-Yu Zhang4, Hong-Xuan Chen1,5,6
1MOE Key Laboratory of Gene Function and Regulation, Guangdong Province Key Laboratory of Pharmaceutical Functional Genes, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, 510275, Guangzhou, China.
The EMBO journal
|June 3, 2025
概括
这项研究揭示了小鼠中广泛的等位基特异性N6 - - 甲基氨酸 (m6A) 甲基化差异,受到序列和父母起源的影响. 这些发现突出了m6A的发现.
科学领域:
- 遗传学 遗传学 是一个
- 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:
- 同基因特异性表达 (ASE) 是通过转录调节的,但对后转录调节的理解仍然较少.
- N6 - - 甲基氨酸 (m6A) 是一种影响基因表达的流行mRNA修饰.
- 研究基因特异性的m6A (ASm6A) 可以发现新的转录后调节机制.
研究的目的:
- 在小鼠中进行异位基因特异性m6A甲基化的全转录组分析.
- 为了识别依赖序列和依赖原产地父的ASm6A.
- 探索ASm6A与等位基特异性表达之间的关系.
主要方法:
- 从不同小鼠菌株的相互交叉交叉的早期产后组织中对m6A的全转录组分析.
- 测量单基分辨率的等位基m6A差异.
- 统计分析以确定显著和可重复的ASm6A网站.
主要成果:
- 确定了成千上万个具有统计意义和可重现的ASm6A位点,表明在m6A甲基化中存在广泛的依赖序列的基失衡.
- 在ASm6A位点附近发现了cis调节变异的证据.
- 检测到父母对m6作为表现出父母来源依赖的ASE的基甲基化的影响.
- 观察到m6A甲基化和表达之间对立的等位基因偏好,无论是依赖于序列还是依赖于原始基因的ASm6As.
结论:
- 无论是cis-acting还是父源效应,都显著影响了等位基特的m6A甲基化.
- ASm6A可以通过对基因表达的负面影响来调节等位基因特异性表达.
- 这项研究为对异位基因特异性表达的转录后调节提供了新的见解.
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