Laboratory of Cell Growth and Differentiation, Institute of Molecular and Cellular Biosciences, the University of Tokyo, Hongo, Bunkyo, Tokyo, Japan.
Division of Cardiovascular Regeneration, Institute of Molecular and Cellular Biosciences, the University of Tokyo, Hongo, Bunkyo, Tokyo, Japan.
BMC Genomics. 2018 Dec 27;19(1):967. doi: 10.1186/s12864-018-5233-5.
Heart development is a relatively fragile process in which many transcription factor genes show dose-sensitive characteristics such as haploinsufficiency and lower penetrance. Despite efforts to unravel the genetic mechanism for overcoming the fragility under normal conditions, our understanding still remains in its infancy. Recent studies on the regulatory mechanisms governing gene expression in mammals have revealed that long non-coding RNAs (lncRNAs) are important modulators at the transcriptional and translational levels. Based on the hypothesis that lncRNAs also play important roles in mouse heart development, we attempted to comprehensively identify lncRNAs by comparing the embryonic and adult mouse heart and brain.
We have identified spliced lncRNAs that are expressed during development and found that lncRNAs that are expressed in the heart but not in the brain are located close to genes that are important for heart development. Furthermore, we found that many important cardiac transcription factor genes are located in close proximity to lncRNAs. Importantly, many of the lncRNAs are divergently transcribed from the promoter of these genes. Since the lncRNA divergently transcribed from Tbx5 is highly evolutionarily conserved, we focused on and analyzed the transcript. We found that this lncRNA exhibits a different expression pattern than that of Tbx5, and knockdown of this lncRNA leads to embryonic lethality.
These results suggest that spliced lncRNAs, particularly bidirectional lncRNAs, are essential regulators of mouse heart development, potentially through the regulation of neighboring transcription factor genes.
心脏发育是一个相对脆弱的过程,许多转录因子基因表现出剂量敏感的特征,如单倍不足和较低的外显率。尽管人们努力揭示正常条件下克服脆弱性的遗传机制,但我们的理解仍处于起步阶段。最近关于哺乳动物基因表达调控机制的研究表明,长非编码 RNA(lncRNA)在转录和翻译水平上是重要的调节剂。基于 lncRNA 也在小鼠心脏发育中发挥重要作用的假设,我们试图通过比较胚胎期和成年期的小鼠心脏和大脑来全面鉴定 lncRNA。
我们已经鉴定了在发育过程中表达的剪接 lncRNA,并发现在心脏中表达而不在大脑中表达的 lncRNA 靠近对心脏发育很重要的基因。此外,我们发现许多重要的心脏转录因子基因位于靠近 lncRNA 的位置。重要的是,许多 lncRNA 是从这些基因的启动子反向转录而来的。由于从 Tbx5 反向转录的 lncRNA 高度进化保守,我们专注于并分析了该转录物。我们发现该 lncRNA 的表达模式与 Tbx5 不同,并且敲低该 lncRNA 会导致胚胎致死。
这些结果表明,剪接的 lncRNA,特别是双向 lncRNA,是小鼠心脏发育的重要调节因子,可能通过调节相邻的转录因子基因。