The stem cell-associated transcription co-factor, ZNF521, interacts with GLI1 and GLI2 and enhances the activity of the Sonic hedgehog pathway

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Stefania Scicchitano
Marco Giordano
Valeria Lucchino
Ylenia Montalcini
Emanuela Chiarella
Annamaria Aloisio
Bruna Codispoti
Pietro Zoppoli
Valentina Melocchi
Fabrizio Bianchi
Enrico De Smaele
Maria Mesuraca
Giovanni Morrone
Heather M. Bond
机构
[1] University Magna Græcia,Laboratory of Molecular Haematopoiesis and Stem Cell Biology, Department of Experimental and Clinical Medicine
[2] European Institute of Oncology IRCCS,Unit of Gynecological Oncology Research
[3] German Center for Neurodegenerative Diseases (DZNE),Laboratory of Pre
[4] Tecnologica Research Institute-Marrelli Hospital,clinical and Translational Research, IRCCS
[5] Referral Cancer Center of Basilicata,CROB
[6] Laboratory of Cancer Biomarkers,Fondazione IRCCS – Casa Sollievo della Sofferenza
[7] University La Sapienza,Department of Experimental Medicine
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ZNF521 is a transcription co-factor with recognized regulatory functions in haematopoietic, osteo-adipogenic and neural progenitor cells. Among its diverse activities, ZNF521 has been implicated in the regulation of medulloblastoma (MB) cells, where the Hedgehog (HH) pathway, has a key role in the development of normal cerebellum and of a substantial fraction of MBs. Here a functional cross-talk is shown for ZNF521 with the HH pathway, where it interacts with GLI1 and GLI2, the major HH transcriptional effectors and enhances the activity of HH signalling. In particular, ZNF521 cooperates with GLI1 and GLI2 in the transcriptional activation of GLI (glioma-associated transcription factor)-responsive promoters. This synergism is dependent on the presence of the N-terminal, NuRD-binding motif in ZNF521, and is sensitive to HDAC (histone deacetylase) and GLI inhibitors. Taken together, these results highlight the role of ZNF521, and its interaction with the NuRD complex, in determining the HH response at the level of transcription. This may be of particular relevance in HH-driven diseases, especially regarding the MBs belonging to the SHH (sonic HH) subgroup where a high expression of ZNF521 is correlated with that of HH pathway components.
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