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一种具有强大转录激活结构域的新型髓系限制性斑马鱼CCAAT/增强子结合蛋白。

A novel myeloid-restricted zebrafish CCAAT/enhancer-binding protein with a potent transcriptional activation domain.

作者信息

Lyons S E, Shue B C, Oates A C, Zon L I, Liu P P

机构信息

National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Blood. 2001 May 1;97(9):2611-7. doi: 10.1182/blood.v97.9.2611.

DOI:10.1182/blood.v97.9.2611
PMID:11313249
Abstract

The CCAAT/enhancer-binding protein (C/EBP) family consists of transcription factors essential for hematopoiesis. The defining feature of the C/EBPs is a highly conserved carboxy-terminal bZIP domain that is necessary and sufficient for dimerization and DNA binding, whereas their amino-terminal domains are unique. This study reports a novel c/ebp gene (c/ebp1) from zebrafish that encodes a protein homologous to mammalian C/EBPs within the bZIP domain, but with an amino terminus lacking homology to any C/EBP or to any known sequence. In zebrafish embryos, c/ebp1 expression was initially observed in cells within the yolk sac circulation valley at approximately the 16-to 18-somite stage, and at 24 hours postfertilization (hpf), also in circulating cells. Most c/ebp1(+) cells also expressed a known early macrophage marker, leukocyte-specific plastin (l-plastin). Expression of both markers was lost in cloche, a mutant affecting hematopoiesis at the level of the hemangioblast. Expression of both markers was retained in m683 and spadetail, mutants affecting erythropoiesis, but not myelopoiesis. Further, c/ebp1 expression was lost in a mutant with defective myelopoiesis, but intact erythropoiesis. These data suggest that c/ebp1 is expressed exclusively in myeloid cells. In electrophoretic mobility shift assays, c/ebp1 was able to bind a C/EBP consensus DNA site. Further, a chimeric protein containing the amino-terminal domain of c/ebp1 fused to the DNA-binding domain of GAL4 induced a GAL4 reporter 4000-fold in NIH3T3 cells. These results suggest that c/ebp1 is a novel member of the C/EBP family that may function as a potent transcriptional activator in myeloid cells.

摘要

CCAAT/增强子结合蛋白(C/EBP)家族由造血过程中必不可少的转录因子组成。C/EBP的决定性特征是一个高度保守的羧基末端碱性亮氨酸拉链(bZIP)结构域,该结构域对于二聚化和DNA结合是必需且足够的,而它们的氨基末端结构域则是独特的。本研究报道了一种来自斑马鱼的新型c/ebp基因(c/ebp1),该基因在bZIP结构域内编码一种与哺乳动物C/EBP同源的蛋白质,但其氨基末端与任何C/EBP或任何已知序列均无同源性。在斑马鱼胚胎中,最初在大约16至18体节期的卵黄囊循环谷内的细胞中观察到c/ebp1表达,在受精后24小时(hpf),也在循环细胞中观察到。大多数c/ebp1(+)细胞还表达一种已知的早期巨噬细胞标志物,白细胞特异性丝束蛋白(l-丝束蛋白)。在cloche突变体中,这两种标志物的表达均缺失,cloche是一种在成血管细胞水平影响造血的突变体。在m683和spadetail突变体中,这两种标志物的表达均保留,这两种突变体影响红细胞生成,但不影响髓细胞生成。此外,在具有缺陷性髓细胞生成但红细胞生成完整的突变体中,c/ebp1表达缺失。这些数据表明c/ebp1仅在髓细胞中表达。在电泳迁移率变动分析中,c/ebp1能够结合C/EBP共有DNA位点。此外,一种包含c/ebp1氨基末端结构域与GAL4 DNA结合结构域融合的嵌合蛋白在NIH3T3细胞中诱导GAL4报告基因表达增强4000倍。这些结果表明c/ebp1是C/EBP家族的一个新成员,可能在髓细胞中作为一种有效的转录激活因子发挥作用。

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