Engreitz Jesse M, Haines Jenna E, Perez Elizabeth M, Munson Glen, Chen Jenny, Kane Michael, McDonel Patrick E, Guttman Mitchell, Lander Eric S
Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA.
Division of Health Sciences and Technology, MIT, Cambridge, Massachusetts 02139, USA.
Nature. 2016 Nov 17;539(7629):452-455. doi: 10.1038/nature20149. Epub 2016 Oct 26.
Mammalian genomes are pervasively transcribed to produce thousands of long non-coding RNAs (lncRNAs). A few of these lncRNAs have been shown to recruit regulatory complexes through RNA-protein interactions to influence the expression of nearby genes, and it has been suggested that many other lncRNAs can also act as local regulators. Such local functions could explain the observation that lncRNA expression is often correlated with the expression of nearby genes. However, these correlations have been challenging to dissect and could alternatively result from processes that are not mediated by the lncRNA transcripts themselves. For example, some gene promoters have been proposed to have dual functions as enhancers, and the process of transcription itself may contribute to gene regulation by recruiting activating factors or remodelling nucleosomes. Here we use genetic manipulation in mouse cell lines to dissect 12 genomic loci that produce lncRNAs and find that 5 of these loci influence the expression of a neighbouring gene in cis. Notably, none of these effects requires the specific lncRNA transcripts themselves and instead involves general processes associated with their production, including enhancer-like activity of gene promoters, the process of transcription, and the splicing of the transcript. Furthermore, such effects are not limited to lncRNA loci: we find that four out of six protein-coding loci also influence the expression of a neighbour. These results demonstrate that cross-talk among neighbouring genes is a prevalent phenomenon that can involve multiple mechanisms and cis-regulatory signals, including a role for RNA splice sites. These mechanisms may explain the function and evolution of some genomic loci that produce lncRNAs and broadly contribute to the regulation of both coding and non-coding genes.
哺乳动物基因组广泛转录产生数千种长链非编码RNA(lncRNA)。其中一些lncRNA已被证明可通过RNA-蛋白质相互作用募集调控复合物,从而影响附近基因的表达,并且有人提出许多其他lncRNA也可作为局部调节因子。这种局部功能可以解释lncRNA表达通常与附近基因表达相关的现象。然而,这些相关性难以剖析,也可能是由lncRNA转录本本身未介导的过程导致的。例如,一些基因启动子被认为具有作为增强子的双重功能,转录过程本身可能通过募集激活因子或重塑核小体来促进基因调控。在这里,我们利用小鼠细胞系中的基因操作来剖析12个产生lncRNA的基因组位点,发现其中5个位点在顺式作用下影响相邻基因的表达。值得注意的是,这些效应均不依赖于特定的lncRNA转录本本身,而是涉及与其产生相关的一般过程,包括基因启动子的增强子样活性、转录过程以及转录本的剪接。此外,这种效应并不局限于lncRNA位点:我们发现六个蛋白质编码位点中有四个也会影响相邻基因的表达。这些结果表明,相邻基因之间的相互作用是一种普遍现象,可能涉及多种机制和顺式调控信号,包括RNA剪接位点的作用。这些机制可能解释了一些产生lncRNA的基因组位点的功能和进化,并广泛参与编码基因和非编码基因的调控。