Kikuchi Kunio, Fukuda Makiha, Ito Tomoya, Inoue Mitsuko, Yokoi Takahide, Chiku Suenori, Mitsuyama Toutai, Asai Kiyoshi, Hirose Tetsuro, Aizawa Yasunori
Center for Biological Resources and Informatics, Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama 226-8501, Japan.
Nucleic Acids Res. 2009 Aug;37(15):4987-5000. doi: 10.1093/nar/gkp426. Epub 2009 Jun 16.
Mammalian transcriptome analysis has uncovered tens of thousands of novel transcripts of unknown function (TUFs). Classical and recent examples suggest that the majority of TUFs may underlie vital intracellular functions as non-coding RNAs because of their low coding potentials. However, only a portion of TUFs have been studied to date, and the functional significance of TUFs remains mostly uncharacterized. To increase the repertoire of functional TUFs, we screened for TUFs whose expression is controlled during differentiation of pluripotent human mesenchymal stem cells (hMSCs). The resulting six TUFs, named transcripts related to hMSC differentiation (TMDs), displayed distinct transcriptional kinetics during hMSC adipogenesis and/or osteogenesis. Structural and comparative genomic characterization suggested a wide variety of biologically active structures of these TMDs, including a long nuclear non-coding RNA, a microRNA host gene and a novel small protein gene. Moreover, the transcriptional response to established pathway activators indicated that most of these TMDs were transcriptionally regulated by each of the two key pathways for hMSC differentiation: the Wnt and protein kinase A (PKA) signaling pathways. The present study suggests that not only TMDs but also other human TUFs may in general participate in vital cellular functions with different molecular mechanisms.
哺乳动物转录组分析发现了数以万计功能未知的新转录本(TUFs)。经典及近期的例子表明,由于其低编码潜能,大多数TUFs可能作为非编码RNA参与重要的细胞内功能。然而,迄今为止仅对一部分TUFs进行了研究,TUFs的功能意义大多仍未明确。为了增加功能性TUFs的种类,我们筛选了在多能性人骨髓间充质干细胞(hMSCs)分化过程中表达受到调控的TUFs。最终得到的六个TUFs,命名为与hMSC分化相关的转录本(TMDs),在hMSC脂肪生成和/或骨生成过程中表现出不同的转录动力学。结构和比较基因组特征表明这些TMDs具有多种生物活性结构,包括一种长链核非编码RNA、一个微小RNA宿主基因和一个新型小蛋白基因。此外,对既定信号通路激活剂的转录反应表明,这些TMDs中的大多数受hMSC分化的两个关键信号通路(Wnt和蛋白激酶A(PKA)信号通路)的转录调控。本研究表明,不仅TMDs,其他人类TUFs通常也可能通过不同分子机制参与重要的细胞功能。