Functional and molecular features of the calmodulin-interacting protein IQCG required for haematopoiesis in zebrafish

We previously reported a fusion protein NUP98–IQCG in an acute leukaemia, which functions as an aberrant regulator of transcriptional expression, yet the structure and function of IQCG have not been characterized. Here we use zebrafish to investigate the role of iqcg in haematopoietic development, a...

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Veröffentlicht in:Nature communications 2014-05, Vol.5 (1), p.3811-3811, Article 3811
Hauptverfasser: Chen, Li-Ting, Liang, Wen-Xue, Chen, Shuo, Li, Ren-Ke, Tan, Jue-Ling, Xu, Peng-Fei, Luo, Liu-Fei, Wang, Lei, Yu, Shan-He, Meng, Guoyu, Li, Keqin Kathy, Liu, Ting-Xi, Chen, Zhu, Chen, Sai-Juan
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Sprache:eng
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Zusammenfassung:We previously reported a fusion protein NUP98–IQCG in an acute leukaemia, which functions as an aberrant regulator of transcriptional expression, yet the structure and function of IQCG have not been characterized. Here we use zebrafish to investigate the role of iqcg in haematopoietic development, and find that the numbers of haematopoietic stem cells and multilineage-differentiated cells are reduced in iqcg -deficient embryos. Mechanistically, IQCG binds to calmodulin (CaM) and acts as a molecule upstream of CaM-dependent kinase IV (CaMKIV). Crystal structures of complexes between CaM and IQ domain of IQCG reveal dual CaM-binding footprints in this motif, and provide a structural basis for a higher CaM–IQCG affinity when deprived of calcium. The results collectively allow us to understand IQCG-mediated calcium signalling in haematopoiesis, and propose a model in which IQCG stores CaM at low cytoplasmic calcium concentrations, and releases CaM to activate CaMKIV when calcium level rises. NUP98–IQCG is a fusion protein found in acute leukaemia that functions as a regulator of transcriptional expression. Here, Chen et al . investigate IQCG-mediated calcium signalling in haematopoiesis, and propose a model where IQCG can store calmodulin, which once released, activates CaM-dependent kinase IV.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms4811