共 2 条
The stem cell zinc finger 1 (SZF1)/ZNF589 protein has a human-specific evolutionary nucleotide DNA change and acts as a regulator of cell viability in the hematopoietic system
被引:7
|作者:
Venturini, Letizia
[1
]
Stadler, Michael
[1
]
Manukjan, Georgi
[2
]
Scherr, Michaela
[1
]
Schlegelberger, Brigitte
[2
]
Steinemann, Doris
[2
]
Ganser, Arnold
[1
]
机构:
[1] Hannover Med Sch, Dept Hematol Hemostasis Oncol & Stem Cell Transpl, Carl Neuberg Str 1, D-30625 Hannover, Germany
[2] Hannover Med Sch, Inst Human Genet, D-30625 Hannover, Germany
关键词:
GENE-EXPRESSION;
COREPRESSOR;
EXPANSION;
HP1;
SELENOCYSTEINE;
RECOGNITION;
HIF-1-ALPHA;
PROGRESSION;
REPRESSION;
SUBFAMILY;
D O I:
10.1016/j.exphem.2015.12.005
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
The stem cell zinc finger 1 (SZF1)/ZNF589 protein belongs to the large family of Kruppel-associated box domain zinc finger (KRAB-ZNF) transcription factors, which are present only in higher vertebrates and epigenetically repress transcription by recruiting chromatin modifying complexes to the promoter regions of their respective target genes. Although the distinct biological functions of most KRAB-ZNF proteins remain unknown, recent publications indicate their implication in fundamental processes, such as cell proliferation, apoptosis, differentiation, development, and tumorigenesis. SZF1/ZNF589 was first identified as a gene with SZF1-1 isoform specifically expressed in CD34(+) hematopoietic cells, strongly suggesting a role in epigenetic control of gene expression in hematopoietic stem/progenitor cells (HSPCs). However, the function of SZF1/ZNF589 in hematopoiesis has not yet been elucidated. Our study reveals SZF1/ZNF589 as a gene with a human-specific nucleotide DNA-change, conferring potential species-specific functional properties. Through shRNA-mediated loss of-function experiments, we found that changes in expression of fundamental apoptosis-controlling genes are induced on SZF1/ZNF589 knockdown, resulting in inhibited growth of hematopoietic cell lines and decreased progenitor potential of primary human bone marrow CD34(+) cells. Moreover, we found that the SZF1/ZNF589 gene is differentially regulated during hypoxia in CD34(+) HSPCs in a cytokine-dependent manner, implicating its possible involvement in the maintenance of the hypoxic physiologic status of hematopoietic stem cells. Our results establish the role of SZF1/ZNF589 as a new functional regulator of the hematopoietic system. Copyright (C) 2016 ISEH - International Society for Experimental Hematology. Published by Elsevier Inc.
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页码:257 / 268
页数:12
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