National Institute of Biological Sciences, Beijing, 102206, China.
Tsinghua Institute of Multidisciplinary Biomedical Research, Tsinghua University, 10084, Beijing, China.
Sci Rep. 2020 Feb 20;10(1):3094. doi: 10.1038/s41598-020-59697-7.
Involvement of long non-coding RNAs (lncRNAs) in the regulation of gene expression in cis has been well studied in eukaryotes but relatively little is known whether and how lncRNAs affect gene expression in tans. In Arabidopsis thaliana, COLDAIR, a previously reported lncRNA, is produced from the first intron of FLOWERING LOCUS C (FLC), which encodes a repressor of flowering time. Our results indicated that the exogenously overexpressed COLDAIR enhances the expression of FLC in trans, resulting in a late-flowering phenotype. In 35S-COLDAIR lines, the enhanced expression of FLC is correlated with the down-regulation of the repressive histone mark H3K27me3 and with the up-regulation of the active histone mark H3K4me3 at the FLC chromatin. Furthermore, we demonstrated that overexpression of intronic lncRNAs from several other H3K27me3-enriched MADS-box genes also activates the expression of their host genes. This study suggests that the involvement of overexpressed intronic lncRNAs in gene activation may be conserved in H3K27me3-enriched genes in eukaryotes.
长链非编码 RNA(lncRNA)在顺式调节基因表达中的作用在真核生物中得到了很好的研究,但关于 lncRNA 是否以及如何影响反式基因表达知之甚少。在拟南芥中,先前报道的 lncRNA COLDAIR 来自开花时间抑制剂 FLOWERING LOCUS C(FLC)的第一个内含子。我们的研究结果表明,外源过表达的 COLDAIR 增强了 FLC 的反式表达,导致开花时间延迟。在 35S-COLDAIR 系中,FLC 的增强表达与抑制性组蛋白标记 H3K27me3 的下调以及 FLC 染色质上活性组蛋白标记 H3K4me3 的上调相关。此外,我们证明来自其他几个富含 H3K27me3 的 MADS-box 基因的内含子 lncRNA 的过表达也激活了其宿主基因的表达。这项研究表明,在富含 H3K27me3 的基因中,过表达的内含子 lncRNA 参与基因激活可能是保守的。