Characterization and evolutionary origin of novel C<sub>2</sub>H<sub>2</sub> zinc finger protein (ZNF648) required for both erythroid and megakaryocyte differentiation in humans
Daniel C.J. Ferguson,
Juraidah Haji Mokim,
Marjolein Meinders,
Edmund R.R. Moody,
Tom A. Williams,
Sarah Cooke,
Kongtana Trakarnsanga,
Deborah E. Daniels,
Ivan Ferrer-Vicens,
Deborah Shoemark,
Chartsiam Tipgomut,
Katherine A. Macinnes,
Marieangela C. Wilson,
Belinda K. Singleton,
Jan Frayne
Affiliations
Daniel C.J. Ferguson
School of Biochemistry, University of Bristol, BS8 1TD, UK.
Juraidah Haji Mokim
School of Biochemistry, University of Bristol, BS8 1TD, UK.
Marjolein Meinders
School of Biochemistry, University of Bristol, BS8 1TD, UK.
Edmund R.R. Moody
School of Biological Sciences, University of Bristol, BS8 1TQ, UK.
Tom A. Williams
School of Biological Sciences, University of Bristol, BS8 1TQ, UK.
Sarah Cooke
School of Biochemistry, University of Bristol, BS8 1TD, UK.
Kongtana Trakarnsanga
Department of Biochemistry, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, 10700, Thailand.
Deborah E. Daniels
School of Biochemistry, University of Bristol, BS8 1TD, UK.; NIHR Blood and Transplant Research Unit in Red blood cell products, University of Bristol, Bristol BS8 1TD, UK.
Ivan Ferrer-Vicens
School of Biochemistry, University of Bristol, BS8 1TD, UK.
Deborah Shoemark
School of Biochemistry, University of Bristol, BS8 1TD, UK.
Chartsiam Tipgomut
Department of Biochemistry, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, 10700, Thailand.
Katherine A. Macinnes
School of Biochemistry, University of Bristol, BS8 1TD, UK.; NIHR Blood and Transplant Research Unit in Red blood cell products, University of Bristol, Bristol BS8 1TD, UK.
Marieangela C. Wilson
School of Biochemistry, University of Bristol, BS8 1TD, UK.
Belinda K. Singleton
NIHR Blood and Transplant Research Unit in Red blood cell products, University of Bristol, Bristol BS8 1TD, UK.; Bristol Institute for Transfusion Sciences, National Health Service Blood and Transplant (NHSBT), Bristol, BS34 7QH, UK
Jan Frayne
School of Biochemistry, University of Bristol, BS8 1TD, UK.; NIHR Blood and Transplant Research Unit in Red blood cell products, University of Bristol, Bristol BS8 1TD, UK.
Human ZNF648 is a novel poly C-terminal C2H2 zinc finger (ZnF) protein identified amongst the most dysregulated proteins in erythroid cells differentiated from induced pluripotent stem cells. Its nuclear localization and structure indicate it is likely a DNA-binding protein. Using a combination of ZNF648 overexpression in an induced pluripotent stem cells line and primary adult erythroid cells, ZNF648 knockdown in primary adult erythroid cells and megakaryocytes, comparative proteomics and transcriptomics we show that ZNF648 is required for both erythroid and megakaryocyte differentiation. Orthologues of ZNF648 were detected across Mammals, Reptilia, Actinopterygii, in some Aves, Amphibia and Coelacanthiformes suggesting the gene originated in the common ancestor of Osteichthyes (Euteleostomi or bony fish). Conservation of the C-terminal ZnF domain is higher, with some variation in ZnF number but a core of at least six ZnF conserved across all groups, with the N-terminus recognisably similar within but not between major lineages. This suggests the N-terminus of ZNF648 evolves faster than the C-terminus, however this is not due to exon-shuffling as the entire coding region of ZNF648 is within a single exon. As for other such transcription factors, the N-terminus likely carries out regulatory functions, but showed no sequence similarity to any known domains. The greater functional constraint on the ZnF domain suggests ZNF648 binds at least some similar regions of DNA in the different organisms. However, divergence of the N-terminal region may enable differential expression, allowing adaptation of function in the different organisms.
