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KMID : 0578320000100010001
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Molecules and Cells
2000 Volume.10 No. 1 p.1 ~ p.7
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The bHLH Gene Hes1 Regulates Differentiation of Multiple Cell Types
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Kageyama, Ryoichiro
Ohtsuka, Toshiyuki/Tomita, Koichi
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Abstract
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For embryos that have small pancreas and lack brain, eyes and thymus, the defects are caused by mutation of a single gene, Hesl. Hesl encodes a basic helix-loop-helix (bHLH) transcriptional repressor and functionally antagonizes positive bHLH genes such as the neuronal determination gene, Mashl. Misexpression of Hesl inhibits cell differentiation and keeps cells at the precursor stage or proliferative stage. Conversely, in the absence of Hesl, the 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. Thus, Hesl regulates tissue morphogenesis by maintaining undifferentiated cells. In the case of T cell development, Hesl mutation leads to defects of expansion of early T cell precursors and thereby suppresses T cell fate specification. Thus, Hesl promotes differentiation of some cell types in addition to maintenance of the undifferentiated state. Interestingly, Hesl expression 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-Hesl pathway, which is controlled by cell-cell interaction, plays an essential role in differentiation of many cell types.
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