[破骨细胞发生过程中的转录组分析和表观遗传学分析]。

Clinical calcium Pub Date : 2016-04-01
Shinya Nakamura, Sakae Tanaka
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引用次数: 0

摘要

1998年发现核因子-κB配体受体激活因子(RANKL)在破骨细胞发生中的重要作用。随后,通过转录组分析,发现RANKL-RANK信号的下游基因Nfatc1是破骨细胞发生的主要调控因子。近年来,随着表观遗传分析方法和大数据分析技术的进步,有关破骨细胞发生的表观遗传分析逐渐深入。最近发表了一些利用破骨细胞发生过程中H3K4me3和H3K27me3组蛋白修饰变化数据、dna -seq数据和甲醛辅助分离调控元件(FAIRE)-seq数据的论文。这可能有助于在未来阐明破骨细胞与成骨细胞、骨细胞或软骨细胞之间的串扰。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Transcriptome analysis and epigenetic analysis during osteoclastogenesis].

The importance of receptor activator of nuclear factor-κB ligand(RANKL)during osteoclastogenesis was discovered in 1998. After that Nfatc1, downstream gene of RANKL-RANK signaling, was identified as a master regulator of osteoclastogenesis by transcriptome analysis. In recent years, with the advancement of epigenetic analysis method and big data analysis technology, epigenetic analysis about osteoclastogenesis gradually progresses. Some papers using H3K4me3 and H3K27me3 histone modification change data, DNase-seq data and formaldehyde-assisted isolation of regulatory elements(FAIRE)-seq data during osteoclastogenesis were published recently. It will probably contribute to elucidate the crosstalk between osteoclasts and osteoblasts, osteocytes or chondrocytes in the future.

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