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Inhibition of touch cell fate by egl-44 and egl-46 in C. elegans
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In wild-type Caenorhabditis elegans, six cells develop as receptors for gentle touch. In egl-44 and egl-46mutants, two other neurons, the FLP cells, express touch receptor-like features. egl-44 and egl-46 also affect the differentiation of other neurons including the HSN neurons, two cells needed for egg laying. egl-44 encodes a member of the transcription enhancer factor family. The product of the egl-46gene, two Drosophila proteins, and two proteins in human and mice define a new family of zinc finger proteins. Both egl-44and egl-46 are expressed in FLP and HSN neurons (and other cells); expression of egl-46 is dependent on egl-44 in the FLP cells but not in the HSN cells. Wild-type touch cells expressegl-46 but not egl-44. Moreover, ectopic expression ofegl-44 in the touch cells prevents touch cell differentiation in an egl-46-dependent manner. The sequences of these genes and their nuclear location as seen with GFP fusions indicate that they repress transcription of touch cell characteristics in the FLP cells.
Title: Inhibition of touch cell fate by egl-44 and egl-46 in C. elegans
Description:
In wild-type Caenorhabditis elegans, six cells develop as receptors for gentle touch.
In egl-44 and egl-46mutants, two other neurons, the FLP cells, express touch receptor-like features.
egl-44 and egl-46 also affect the differentiation of other neurons including the HSN neurons, two cells needed for egg laying.
egl-44 encodes a member of the transcription enhancer factor family.
The product of the egl-46gene, two Drosophila proteins, and two proteins in human and mice define a new family of zinc finger proteins.
Both egl-44and egl-46 are expressed in FLP and HSN neurons (and other cells); expression of egl-46 is dependent on egl-44 in the FLP cells but not in the HSN cells.
Wild-type touch cells expressegl-46 but not egl-44.
Moreover, ectopic expression ofegl-44 in the touch cells prevents touch cell differentiation in an egl-46-dependent manner.
The sequences of these genes and their nuclear location as seen with GFP fusions indicate that they repress transcription of touch cell characteristics in the FLP cells.
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