| Literature DB >> 30959201 |
Yue Tang1, Shanshan Ma2, Xinxin Wang3, Qu Xing2, Tuanjie Huang2, Hongtao Liu2, Qinghua Li2, Yanting Zhang2, Kun Zhang2, Minghao Yao2, Greta Luyuan Yang4, Hui Li5, Xingxing Zang6, Bo Yang7, Fangxia Guan8.
Abstract
Chimeric RNAs are transcripts composed of RNA fragments from different genes and are traditionally well-known cancer-causing genetic events. Recent studies show chimeric RNAs being present in multiple non-neoplastic tissues and cells, suggesting that at least some may have roles in normal physiology. However, chimeric RNAs and their implications in brain development and neural differentiation have not been formally studied. Here, we firstly characterized the landscape of chimeric RNAs in human infant brain tissues and identified 599 chimeric RNAs. Through a series of filtering, 22 were selected and tested in a neural differentiation process starting from stem cells. Ten were validated experimentally. One of these ten chimeric RNAs, DUS4L-BCAP29, dramatically increased when human umbilical mesenchymal stem cells were induced for neural differentiation. Consistently, we found that overexpressed DUS4L-BCAP29 effectively promoted neural differentiation. Our results support the important role(s) chimeric RNAs play in neural differentiation, and are consistent with the new notion that chimeric RNAs also exist in normal physiology, and likely serve biological purposes.Entities:
Keywords: Brain; Chimeric RNAs; DUS4L-BCAP29; Mesenchymal stem cells; Neural differentiation
Year: 2019 PMID: 30959201 DOI: 10.1016/j.biocel.2019.03.012
Source DB: PubMed Journal: Int J Biochem Cell Biol ISSN: 1357-2725 Impact factor: 5.085