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Functional and molecular features of the calmodulin-interacting protein IQCG required for haematopoiesis in zebrafish.
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.
Afiliação
  • Chen LT; 1] State Key Laboratory of Medical Genomics and Shanghai, Institute of Hematology, Rui Jin Hospital affiliated to Shanghai Jiao Tong University (SITU) School of Medicine, Shanghai, 200025, China [2] Institute of Health Sciences, Shanghai Institutes for Biological Sciences and Graduate School, Chines
  • Liang WX; 1] Central Laboratory, Lianyungang First People's Hospital, Lianyungang 222002, China [2].
  • Chen S; 1] Ludwig Institute for Cancer Research, Old Road Campus Research Building, University of Oxford, Roosevelt Drive, Oxford OX3 7DQ, UK [2].
  • Li RK; 1] State Key Laboratory of Medical Genomics and Shanghai, Institute of Hematology, Rui Jin Hospital affiliated to Shanghai Jiao Tong University (SITU) School of Medicine, Shanghai, 200025, China [2] Institute of Health Sciences, Shanghai Institutes for Biological Sciences and Graduate School, Chines
  • Tan JL; State Key Laboratory of Medical Genomics and Shanghai, Institute of Hematology, Rui Jin Hospital affiliated to Shanghai Jiao Tong University (SITU) School of Medicine, Shanghai, 200025, China.
  • Xu PF; State Key Laboratory of Medical Genomics and Shanghai, Institute of Hematology, Rui Jin Hospital affiliated to Shanghai Jiao Tong University (SITU) School of Medicine, Shanghai, 200025, China.
  • Luo LF; State Key Laboratory of Medical Genomics and Shanghai, Institute of Hematology, Rui Jin Hospital affiliated to Shanghai Jiao Tong University (SITU) School of Medicine, Shanghai, 200025, China.
  • Wang L; Institute of Health Sciences, Shanghai Institutes for Biological Sciences and Graduate School, Chinese Academy of Sciences and SITU School of Medicine, Shanghai 200025, China.
  • Yu SH; State Key Laboratory of Medical Genomics and Shanghai, Institute of Hematology, Rui Jin Hospital affiliated to Shanghai Jiao Tong University (SITU) School of Medicine, Shanghai, 200025, China.
  • Meng G; State Key Laboratory of Medical Genomics and Shanghai, Institute of Hematology, Rui Jin Hospital affiliated to Shanghai Jiao Tong University (SITU) School of Medicine, Shanghai, 200025, China.
  • Li KK; State Key Laboratory of Medical Genomics and Shanghai, Institute of Hematology, Rui Jin Hospital affiliated to Shanghai Jiao Tong University (SITU) School of Medicine, Shanghai, 200025, China.
  • Liu TX; State Key Laboratory of Medical Genomics and Shanghai, Institute of Hematology, Rui Jin Hospital affiliated to Shanghai Jiao Tong University (SITU) School of Medicine, Shanghai, 200025, China.
  • Chen Z; State Key Laboratory of Medical Genomics and Shanghai, Institute of Hematology, Rui Jin Hospital affiliated to Shanghai Jiao Tong University (SITU) School of Medicine, Shanghai, 200025, China.
  • Chen SJ; 1] State Key Laboratory of Medical Genomics and Shanghai, Institute of Hematology, Rui Jin Hospital affiliated to Shanghai Jiao Tong University (SITU) School of Medicine, Shanghai, 200025, China [2] Institute of Health Sciences, Shanghai Institutes for Biological Sciences and Graduate School, Chines
Nat Commun ; 5: 3811, 2014 May 02.
Article em En | MEDLINE | ID: mdl-24787902
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Calmodulina / Proteínas de Peixe-Zebra Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Calmodulina / Proteínas de Peixe-Zebra Idioma: En Ano de publicação: 2014 Tipo de documento: Article