Transcripts of unknown function in multiple-signaling pathways involved in human stem cell differentiation

被引:49
作者
Kikuchi, Kunio [1 ]
Fukuda, Makiha [2 ]
Ito, Tomoya [2 ]
Inoue, Mitsuko [2 ]
Yokoi, Takahide [3 ]
Chiku, Suenori [4 ]
Mitsuyama, Toutai [5 ]
Asai, Kiyoshi [5 ,6 ]
Hirose, Tetsuro [7 ]
Aizawa, Yasunori [1 ]
机构
[1] Tokyo Inst Technol, Ctr Biol Resources & Informat, Yokohama, Kanagawa 2268501, Japan
[2] Tokyo Inst Technol, Grad Sch Biosci & Biotechnol, Yokohama, Kanagawa 2268501, Japan
[3] Hitachi Software Engn Co Ltd, Yokohama, Kanagawa 2300045, Japan
[4] Mizuho Informat & Res Inst Inc, Sci Solut Div, Tokyo 1018443, Japan
[5] Natl Inst Adv Ind Sci & Technol, CBRC, Tokyo 1350064, Japan
[6] Univ Tokyo, Grad Sch Frontier Sci, Dept Computat Biol, Chiba 2778561, Japan
[7] Natl Inst Adv Ind Sci & Technol, Funct RNom Team, Biomed Informat Res Ctr, Tokyo 1350064, Japan
关键词
BINDING PROTEIN-ALPHA; NONCODING RNAS; REGULATORY RNAS; MESSENGER-RNA; PPAR-GAMMA; EXPRESSION; PROLIFERATION; ADIPOGENESIS; SUPPRESSES; ACTIVATION;
D O I
10.1093/nar/gkp426
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
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.
引用
收藏
页码:4987 / 5000
页数:14
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