From: LncRNAs and their RBPs: How to influence the fate of stem cells?
LncRNA | RBPs | Cell type | Biological function | Regulatory mechanism | References |
---|---|---|---|---|---|
MEG3 | EZH2 | hDFSC | Promote the osteogenic differentiation of hDFSC | MEG3 interacts with EZH2, down-regulation of MEG3 or EZH2 reduces the occupation of H3K27me3 on the Wnt gene promoter | [51] |
Oct4P4 | SUV39H1 HMTase | mESC | Inhibit the self-renewal of mESC | OctP4 combines with SUV39, H1 and HMTase to form a complex, recruits H3K9me3 and HP1α to the Oct4 promoter region and results in Oct4 silencing | [52] |
ES1, ES2, ES3 | SUZ12 and Sox2 | hESC | Maintain the pluripotency of hESC | ES1, ES2 and ES3 interact with SUZ12 and Sox2, which are the components of PRC2 complex | [53] |
Linc1614 | PRC2 complex and Sox2 | mESC | Maintain the pluripotency of mESC | Linc1614 interacts with Sox2, recruits the PRC2 complex to T, Eomes, and Pitx2 and other developmental gene regions and inhibits their expression | [54] |
LncPRESS1 | SIRT6 | mESC | Maintain the pluripotency of mESC | LncPRESS1 interacts with SIRT6 and inhibits SIRT6 from attaching to chromatin, maintaining the acetylation level of Histone H3K56 and H3K9 on the promoters of pluripotent genes such as Oct4 and Nanog | [55] |
LBCS | hnRNPK and EZH2 | BCSC | Inhibit the self-renewal of BCSC | LBCS binds hnRNPK and EZH2 to form the hnRNPK-EZH2 complex, guides the complex to the Sox2 promoter and H3K27me3 to inhibit Sox2 expression | [56] |
LincU | Dusp9 | mESC | Maintain the pluripotency of mESC | LincU binds and stabilizes ERK-specific phosphatase DUSP to restrict MAPK/ERK activity | [57] |
Trincr1 | Trim71 | mESC | Promote the proliferation of mESC | Thoc5 regulates the export of Trincr1 to the cytoplasm, lncRNA Trincr1 binds to Trim71 in the cytoplasm, inhibits the activity of SHCBP1 and phosphorylates ERK and promotes the expression of ERK pathway target genes | [58] |
Linc1557 | STAT3 | mESC | Promote the self-renewal of mESC | Linc1557 interacts with STAT3 through specific binding sites to regulate the stability of its mRNA, thus regulating the LIF/STAT3 signaling pathway | [60] |
hFAST | β- TrCP | hESC | Maintain the pluripotency of hESC | hFAST binds to WD40 domain of β- TrCP, impedes the interaction between β- TrCP and phosphorylated β-catenin and promotes Wnt activity | [62] |
LncR492 | HuR | mESC | Inhibit the neuroectodermal differentiation of mESC | LncR492 interacts with HuR and activates Wnt signaling | [64] |
TCF7 | BAF170 and SWI/SNF complex | liver CSC | Promote the self-renewal of liver CSC | TCF binds to BAF170 and recruits the SWI/SNF complex to the TCF7 promoter to regulate its expression, leading to the activation of Wnt signaling | [65] |
H19 | EZH2 | hDPSC | Promote the dentin differentiation and proliferation of hDPSC | H19 recruits EZH2 to the LATS1 promoter region to induce H3K27me3, inhibiting the expression of LATS1, blocking the activation of the Hippo-YAP signaling pathway | [68] |
HAND2-AS1 | INO80 complex | live CSC | Promote the self-renewal of liver CSC | HAND2-AS1 combines with INO80 complex to promote the expression of BMPR1A and activate the BMP signaling | [71] |
MALAT1 | SRSF2 | hASC | promote the Proliferation of neurons in the brain injury site of hASC | MALAT1 promotes the splicing of PKCδII by binding with SRSF2 | [73] |
tsRMST | Nanog and SUZ12 | hESC | Inhibit the differentiation of hESC | tsRMST interacts with Nanog and SUZ12 to form a complex and inhibits the expression of Wnt5A through differentiation-related transcription factors, and inhibits non-standard Wnt pathway | [79] |
Pnky | PTBP1 | NSC | Inhibit the differentiation of NSC | Pnky interacts with PTBP1 to maintain the stability of its mRNA | |
ANCR | PTBP1 | hAMSC | Inhibit the differentiation of hAMSC into DE cell | ANCR binds to PTBP1, promotes the interaction between PTBP1 and ID2 mRNA and enhances the stability of ID2 mRNA | [93] |
KB-1980E6.3 | IGF2BP1 | BCSC | Promote the stemness and proliferation of BCSC | KB-1980E6.3 binds to IGF2BP1 to form a complex under the induction of HIF-1α to recognize and enhance the stability of c-myc mRNA | [94] |