| Literature DB >> 24787902 |
Li-Ting Chen1, Wen-Xue Liang2, Shuo Chen3, Ren-Ke Li4, Jue-Ling Tan5, Peng-Fei Xu5, Liu-Fei Luo5, Lei Wang6, Shan-He Yu5, Guoyu Meng5, Keqin Kathy Li5, Ting-Xi Liu5, Zhu Chen5, Sai-Juan Chen4.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2014 PMID: 24787902 DOI: 10.1038/ncomms4811
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919