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巨核细胞生成中 Gata1 和 NF-E2 p45 基因表达的层次调节的遗传分析。

Genetic analysis of hierarchical regulation for Gata1 and NF-E2 p45 gene expression in megakaryopoiesis.

机构信息

Center of Radioisotope Science, Tohoku University Graduate School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai 980-8575, Japan.

出版信息

Mol Cell Biol. 2010 Jun;30(11):2668-80. doi: 10.1128/MCB.01304-09. Epub 2010 Mar 29.

Abstract

GATA1 and NF-E2 p45 are two important regulators of megakaryopoiesis. Whereas GATA1 is known to regulate the p45 gene, details of the GATA1 contribution to the spatiotemporal expression of the p45 gene remain to be elucidated. To clarify the relationship between GATA1 and p45, we performed genetic complementation rescue analysis of p45 function in megakaryocytes utilizing the hematopoietic regulatory domain of the Gata1 gene (G1HRD). We established transgenic mouse lines expressing p45 under G1HRD regulation and crossed the mice with p45-null mice. Compound mutant mice displayed normal platelet counts and no sign of hemorrhage, indicating that G1HRD has the ability to express p45 in a spatiotemporally correct manner. However, deletion of 38 amino acids from the N-terminal region of p45 abrogated the p45 rescue function, suggesting the presence of an essential transactivation activity in the region. We then crossed the G1HRD-p45 transgenic mice with megakaryocyte-specific Gata1 gene knockdown (Gata1(Delta)(neo)(Delta)(HS)) mice. The G1HRD-p45 transgene was insufficient for complete rescue of the Gata1(Delta)(neo)(Delta)(HS) megakaryocytes, suggesting that GATA1 or other factors regulated by GATA1 are required to cooperate with p45 for normal megakaryopoiesis. This study thus provides a unique in vivo validation of the hierarchical relationship between GATA1 and p45 in megakaryocytes.

摘要

GATA1 和 NF-E2 p45 是巨核细胞生成的两个重要调节因子。虽然 GATA1 已知可调节 p45 基因,但 GATA1 对 p45 基因时空表达的贡献细节仍有待阐明。为了阐明 GATA1 和 p45 之间的关系,我们利用 Gata1 基因的造血调节结构域(G1HRD)对巨核细胞中 p45 功能进行了遗传互补拯救分析。我们建立了在 G1HRD 调控下表达 p45 的转基因小鼠系,并将这些小鼠与 p45 缺失型小鼠进行杂交。复合突变小鼠表现出正常的血小板计数,没有出血迹象,表明 G1HRD 具有在时空上正确表达 p45 的能力。然而,从 p45 的 N 端缺失 38 个氨基酸完全消除了 p45 的拯救功能,这表明该区域存在必需的转录激活活性。然后,我们将 G1HRD-p45 转基因小鼠与巨核细胞特异性 Gata1 基因敲除(Gata1(Delta)(neo)(Delta)(HS)小鼠进行杂交。G1HRD-p45 转基因不足以完全拯救 Gata1(Delta)(neo)(Delta)(HS)巨核细胞,这表明 GATA1 或 GATA1 调节的其他因子与 p45 一起对于正常的巨核细胞生成是必需的。因此,本研究为 GATA1 和 p45 在巨核细胞中的层级关系提供了独特的体内验证。

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