The Kleisin Subunits of Cohesin Are Involved in the Fate Determination of Embryonic Stem Cells

Abstract

As a potential candidate to generate an everlasting cell source to treat various diseases, embryonic stem cells are regarded as a promising therapeutic tool in the regenerative medicine field. Cohesin, a multi-functional complex that controls various cellular activities, plays roles not only in organizing chromosome dynamics but also in controlling transcriptional activities related to self-renewal and differentiation of stem cells. Here, we report a novel role of the α-kleisin subunits of cohesin (RAD21 and REC8) in the maintenance of the balance between these two stem-cell processes. By knocking down REC8, RAD21, or the non-kleisin cohesin subunit SMC3 in mouse embryonic stem cells, we show that reduction in cohesin level impairs their self-renewal. Interestingly, the transcriptomic analysis revealed that knocking down each cohesin subunit enables the differentiation of embryonic stem cells into specific lineages. Specifically, embryonic stem cells in which cohesin subunit RAD21 were knocked down differentiated into cells expressing neural alongside germline lineage markers. Thus, we conclude that cohesin appears to control the fate determination of embryonic stem cells.

α-Kleisin subunit of cohesin preserves the genome integrity of embryonic stem cells

“…Therefore, we classified KEGG pathways according to the number of genes whose expression levels were differentially regulated by REC8 or RAD21 depletion. Furthermore, the depletion of each cohesin factor enables the differentiation of ESCs into specific cell-type lineages ( 19 ).…”