摘要：SummaryJAM-A is a tight-junction-associated protein that contributes to regulation of intestinal homeostasis. We report that JAM-A interacts with NF2 and LATS1, functioning as an initiator of the Hippo signaling pathway, well-known for regulation of proliferation. Consistent with these findings, we observed increased YAP activity in JAM-A-deficient intestinal epithelial cells (IEC). Furthermore, overexpression of a dimerization-deficient mutant, JAM-A-DL1, failed to initiate Hippo signaling, phenocopying JAM-A-deficient IEC, whereas overexpression of JAM-A-WT activated Hippo signaling and suppressed proliferation. Lastly, we identify EVI1, a transcription factor reported to promote cellular proliferation, as a contributor to the pro-proliferative phenotype in JAM-A-DL1 overexpressing IEC downstream of YAP. Collectively, our findings establish a new role for JAM-A as a cell-cell contact sensor, raising implications for understanding the contribution(s) of JAM-A to IEC proliferation in the mammalian epithelium.Graphical abstractDisplay OmittedHighlights•JAM-A suppresses intestinal epithelial proliferation through the Hippo pathway•NF2 and LATS1 interact with the JAM-A signaling complex•JAM-A dimerization is a required signaling to initiate Hippo signaling•EVI1 is a driver of the pro-proliferative phenotype of JAM-A-deficient IECBiological sciences; Biochemistry; Cell biology
