Holocarboxylase synthetase acts as a biotin-independent transcriptional repressor interacting with HDAC1, HDAC2 and HDAC7

In human cells, HCS catalyzes the biotinylation of biotin-dependent carboxylases and mediates the transcriptional control of genes involved in biotin metabolism through the activation of a cGMP-dependent signal transduction pathway. HCS also targets to the cell nucleus in association with lamin-B su...

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Veröffentlicht in:Molecular genetics and metabolism 2014-03, Vol.111 (3), p.321-330
Hauptverfasser: Trujillo-Gonzalez, Isis, Cervantes-Roldan, Rafael, Gonzalez-Noriega, Alfonso, Michalak, Colette, Reyes-Carmona, Sandra, Barrios-Garcia, Tonatiuh, Meneses-Morales, Ivan, Leon-Del-Rio, Alfonso
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Sprache:eng
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