Liu Ting Xi, Rhodes Jennifer, Deng Min, Hsu Karl, Radomska Hanna S, Kanki John P, Tenen Daniel G, Look A Thomas
Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Exp Hematol. 2007 Feb;35(2):230-9. doi: 10.1016/j.exphem.2006.10.008.
We investigated the role of CCAAT enhancer-binding protein-alpha (C/EBPalpha) during zebrafish embryonic blood development.
Whole-mount mRNA in situ hybridization was performed to determine the spatio-temporal expression pattern of zebrafish cebpa in developing hematopoietic progenitors. A deletion mutation of cebpa (zD420), which mimics the human dominant-negative mutations of C/EBPalpha, was transfected into CV1 cell line to evaluate its transcriptional activity in vitro and injected into zebrafish embryos at the one- to two-cell stage to examine its effects on primitive hematopoiesis during early zebrafish development.
Zebrafish cebpa is expressed in the anterior and posterior lateral plate mesoderm at 12 hours postfertilization, along with scl, pu.1, and gata1 in developing hematopoietic progenitors. In vitro, the deletion mutation of cebpa (zD420) prevents expression of the full-length protein, allowing the expression of truncated isoforms from internal translational initiation sites. As in the human, the truncated zebrafish C/EBPalpha proteins did not activate the expression of known target granulocytic genes, and in fact suppressed transactivation that was induced in vitro by the full-length protein. Forced expression of the zD420 mRNA in zebrafish embryos led to an expansion of primitive erythropoiesis, without a discernible effect on granulopoiesis.
Expression of the truncated isoforms of cebpa alters the developmental pattern of hematopoietic progenitor cells during embryogenesis.
我们研究了CCAAT增强子结合蛋白α(C/EBPα)在斑马鱼胚胎血液发育过程中的作用。
进行全胚胎mRNA原位杂交,以确定斑马鱼cebpa在发育中的造血祖细胞中的时空表达模式。将模拟人类C/EBPα显性负性突变的cebpa缺失突变体(zD420)转染到CV1细胞系中,以评估其体外转录活性,并在单细胞至双细胞阶段注射到斑马鱼胚胎中,以检查其对斑马鱼早期发育过程中原始造血的影响。
斑马鱼cebpa在受精后12小时在前侧和后侧侧板中胚层表达,与发育中的造血祖细胞中的scl、pu.1和gata1一起表达。在体外,cebpa的缺失突变体(zD420)阻止全长蛋白的表达,允许从内部翻译起始位点表达截短的异构体。与人类情况一样,截短的斑马鱼C/EBPα蛋白不激活已知靶粒细胞基因的表达,实际上还抑制了全长蛋白在体外诱导的反式激活。在斑马鱼胚胎中强制表达zD420 mRNA导致原始红细胞生成增加,对粒细胞生成没有明显影响。
cebpa截短异构体的表达改变了胚胎发生过程中造血祖细胞的发育模式。