Noncoding RNAs in the Regulation of Pluripotency and Reprogramming

被引:31
|
作者
Sherstyuk, Vladimir V. [1 ,2 ,3 ,4 ]
Medvedev, Sergey P. [1 ,2 ,3 ,4 ]
Zakian, Suren M. [1 ,2 ,3 ,4 ]
机构
[1] Russian Acad Sci, Siberian Branch, Fed Res Ctr, Inst Cytol & Genet, 10 Lavrentyeva Ave, Novosibirsk 630090, Russia
[2] Minist Healthcare Russian Federat, E Meshalkin Natl Med Res Ctr, 15 Rechkunovskaya St, Novosibirsk 630055, Russia
[3] Russian Acad Sci, Inst Chem Biol & Fundamental Med, Siberian Branch, 8 Lavrentyeva Ave, Novosibirsk 630090, Russia
[4] Novosibirsk State Univ, 2 Pirogova St, Novosibirsk 630090, Russia
基金
俄罗斯科学基金会;
关键词
Pluripotent stem cells; Pluripotency; Reprogramming; Noncoding RNA; MicroRNA; Long noncoding RNA; Genome editing; CRISPR/Cas9; EMBRYONIC STEM-CELLS; SMALL NUCLEOLAR RNA; GROUND-STATE; TRANSCRIPTIONAL REPRESSORS; MESENCHYMAL TRANSITION; WIDE IDENTIFICATION; PROFILING REVEALS; MIRNA EXPRESSION; DNA METHYLATION; MIR-200; FAMILY;
D O I
10.1007/s12015-017-9782-9
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Pluripotent stem cells have great potential for developmental biology and regenerative medicine. Embryonic stem cells, which are obtained from blastocysts, and induced pluripotent stem cells, which are generated by the reprogramming of somatic cells, are two main types of pluripotent cells. It is important to understand the regulatory network that controls the pluripotency state and reprogramming process. Various types of noncoding RNAs (ncRNAs) have emerged as substantial components of regulatory networks. The most studied class of ncRNAs in the context of pluripotency and reprogramming is microRNAs (miRNAs). In addition to canonical microRNAs, other types of small RNAs with miRNA-like function are expressed in PSCs. Another class of ncRNAs, long ncRNAs, are also involved in pluripotency and reprogramming regulation. Thousands of ncRNAs have been annotated to date, and a significant number of the molecules do not have known function. In this review, we briefly summarized recent advances in this field and described existing genome-editing approaches to study ncRNA functions.
引用
收藏
页码:58 / 70
页数:13
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