PT  - JOURNAL ARTICLE
AU  - Karim Rahimi
AU  - Sara Parsa
AU  - Mehrnoush Nikzaban
AU  - Seyed Javad Mowla
AU  - Fardin Fathi
TI  - Transgenic Mice and Pluripotent Stem Cells Express EGFP under the Control of miR-302 Promoter
AID  - 10.1101/450791
DP  - 2018 Jan 01
TA  - bioRxiv
PG  - 450791
4099  - http://biorxiv.org/content/early/2018/10/23/450791.short
4100  - http://biorxiv.org/content/early/2018/10/23/450791.full
AB  - MicroRNAs are a group of short non-coding RNAs that undertake various roles in different cell signaling pathways and developmental stages. They regulate gene expression levels at the post-transcriptional stage, which results in cleavage of mRNAs or repression of their translation. Some miRNAs, including the miR-302 cluster, are critical regulators for the stemness state of embryonic stem cells and cell fate patterning. The miR-302 cluster is located in the intron of a non-coding gene that has no other reported function, other than hosting miR-302, and grant a complex expression regulation through upstream its regulatory sequences. To date, analysis of the miR-302 expression pattern in a transgenic mouse model has not been reported. In this study, we generated transgenic mice that expressed EGFP driven by miR-302 upstream regulatory sequences that harbored the core promoter of its host gene. We examined the activity of the miR-302 promotor in somatic tissues of transgenic mice, transgenic blastocysts, and embryonic stem cells derived from transgenic blastocysts. Our results showed that miR-302 highly expressed in both blastocysts and the first passages of transgenic embryonic stem cells, and has low expression in the somatic tissues of transgenic mice. It could be concluded that different temporal and spatial gene expression patterns occur during the embryonic and adult stages in mice.