The bHLH gene Hes1 regulates differentiation of multiple cell types

For embryos that have small pancreas and lack brain, eyes and thymus, the d efects are caused by mutation of a single gene, Hes1. Hes1 encodes a basic helix-loop-helix (bHLH) transcriptional repressor and functionally antagoni zes positive bHLH genes such as the neuronal determination gene, Mash1, Mis expression of Hes1 inhibits cell differentiation and keeps cells at the pre cursor stage or proliferative stage. Conversely, in the absence of Hes1, th e expression of positive bHLH genes is upregulated and cells differentiate prematurely without sufficient cell growth. As a result, the development of many tissues such as the brain, eye and pancreas is severely affected. Thu s, Hes1 regulates tissue morphogenesis by maintaining undifferentiated cell s. In the case of T cell development, Hes1 mutation leads to defects of exp ansion of early T cell precursors and thereby suppresses T cell fate specif ication. Thus, Hes1 promotes differentiation of some cell types in addition to maintenance of the undifferentiated state. Interestingly, Hes1 expressi on is controlled by the transmembrane protein Notch, which is activated by the ligands expressed on the surface of neighboring cells. Taken together, these results indicate that the Notch-Hes1 pathway, which is controlled by cell-cell interaction, plays an essential role in differentiation of many c ell types.