Scratch2, a Snail Superfamily Member, Is Regulated by miR-125b

被引:2
作者
Goes, Carolina Purcell [1 ,2 ]
Vieceli, Felipe Monteleone [1 ]
De La Cruz, Shirley Mirna [1 ]
Simoes-Costa, Marcos [2 ]
Yan, Chao Yun Irene [1 ]
机构
[1] Univ Sao Paulo, Inst Biomed Sci, Dept Cell & Dev Biol, Sao Paulo, Brazil
[2] Cornell Univ, Coll Agr & Life Sci, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
基金
巴西圣保罗研究基金会;
关键词
Scratch2; Snail superfamily; miRNA; neural tube; CRISPR; Cas9; EPITHELIAL-MESENCHYMAL TRANSITION; MIR-200; FAMILY; MICRORNA EXPRESSION; GENE-EXPRESSION; CHICK-EMBRYO; TGF-BETA; TRANSCRIPTION; REPRESSION; MIGRATION; TARGETS;
D O I
10.3389/fcell.2020.00769
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Scratch2is a transcription factor expressed in a very restricted population of vertebrate embryonic neural cell precursors involved in their survival, differentiation, and migration. The mechanisms that control its expression remain unknown and could contribute towards our understanding of gene regulation during neural differentiation and evolution. Here we investigate the role of microRNAs (miRNAs) in the Scrt2 post-transcriptional regulatory mechanism. We identified binding sites for miR-125b and -200b in the Scrt2 3 ' UTR in silico. We confirmed the repressive-mediated activity of the Scrt2 3 ' UTR through electroporation of luciferase constructs into chick embryos. Further, both CRISPR/Cas9-mediated deletion of miR-125b/-200b responsive elements from chicken Scrt2 3 ' UTR and expression of miRNAs sponges increased Scrt2 expression field, suggesting a role for these miRNAs as post-transcriptional regulators of Scrt2. The biological effect of miR-125b titration was much more pronounced than that of miR-200b. Therefore, we propose that, after transcription, miR-125b fine-tunes the Scrt2 expression domain.
引用
收藏
页数:10
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