S100C/A11 (red) moves to the nucleus when TGFβ is present (right).
The group previously showed that high extracellular Ca2+ results in phosphorylation of cytoplasmic S100C/A11, driving it into the nucleus. Once there, it releases the transcription factor Sp1 from its binding partner, nucleolin, so that Sp1 can activate p21(WAF1/CIP1) transcription to halt division in skin cells.
The new results demonstrate that this S100C/A11 pathway requires PKCα-mediated phosphorylation of S100C/A11 and, like the Smad pathway, is triggered by TGFβ. Both branches are needed to stop skin cell...
The Rockefeller University Press
2004
The Rockefeller University Press
2004
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