Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine, Tel Aviv University, Ramat Aviv 69978, Israel.
Nucleic Acids Res. 2019 Jul 9;47(12):6145-6159. doi: 10.1093/nar/gkz338.
Chromatin organization and epigenetic markers influence splicing, though the magnitudes of these effects and the mechanisms are largely unknown. Here, we demonstrate that linker histone H1.5 influences mRNA splicing. We observed that linker histone H1.5 binds DNA over splice sites of short exons in human lung fibroblasts (IMR90 cells). We found that association of H1.5 with these splice sites correlated with the level of inclusion of alternatively spliced exons. Exons marked by H1.5 had more RNA polymerase II (RNAP II) stalling near the 3' splice site than did exons not associated with H1.5. In cells depleted of H1.5, we showed that the inclusion of five exons evaluated decreased and that RNAP II levels over these exons were also reduced. Our findings indicate that H1.5 is involved in regulation of splice site selection and alternative splicing, a function not previously demonstrated for linker histones.
染色质结构和表观遗传标记会影响剪接,但这些影响的程度和机制在很大程度上是未知的。在这里,我们证明连接组蛋白 H1.5 会影响 mRNA 的剪接。我们观察到,在人类肺成纤维细胞(IMR90 细胞)中,连接组蛋白 H1.5 结合在短外显子的剪接位点上的 DNA。我们发现 H1.5 与这些剪接位点的结合与选择性剪接外显子的包含水平相关。与 H1.5 结合的外显子在 3'剪接位点附近有更多的 RNA 聚合酶 II(RNAP II)停滞,而与 H1.5 不结合的外显子则没有。在 H1.5 耗尽的细胞中,我们发现评估的五个外显子的包含减少,并且这些外显子上的 RNAP II 水平也降低。我们的研究结果表明,H1.5 参与调节剪接位点选择和选择性剪接,这是连接组蛋白以前未表现出的功能。