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Cul4a promotes zebrafish primitive erythropoiesis via upregulating scl and gata1 expression

机译:CUL4A通过上调SCL和GATA1表达来促进斑马鱼原语红细胞生成

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CUL4A and CUL4B are closely related members in Cullin family and can each assemble a Cullin-RING E3 ligase complex (Cullin-RING Ligase 4A or 4B, CRL4A, or CRL4B) and participate in a variety of biological processes. Previously we showed that zebrafish cul4a, but not cul4b, is essential for cardiac and pectoral fin development. Here, we have identified cul4a as a crucial regulator of primitive erythropoiesis in zebrafish embryonic development. Depletion of cul4a resulted in a striking reduction of erythroid cells due to the inhibition of erythroid differentiation. Transcript levels for early hematopoietic regulatory genes including scl, lmo2, and gata1 are significantly reduced in cul4a-deficient embryos. Mechanistically, we demonstrated that scl and gata1, the central regulators of primitive hematopoiesis for erythroid determination, are transcriptionally upregulated by cul4a. These findings demonstrate an important role for cul4a in primitive erythropoiesis and may bear implications in regeneration medicine of anemia and related diseases.
机译:CUL4A和CUL4B在Cullin系列中是密切相关的构件,并且每个含量可以组装Cullin环E3连接酶复合物(Cullin-环形连接酶4a或4b,Crl4a或Crl4b)并参与各种生物过程。此前我们展示斑马鱼CUL4A,但不是CUL4B,对心脏和胸鳍开发至关重要。在这里,我们已经确定了CUL4A作为斑马鱼胚胎发育中原始红细胞的关键调节因子。由于抑制红细胞分化,Cul4a的耗尽导致红细胞细胞的减少。在CUL4A缺陷的胚胎中显着降低了包括SCL,LMO2和GATA1,包括SCL,LMO2和GATA1的早期造血调节基因的转录水平。机械地,我们证明了SCL和GATA1,原始血液血液的中央调节因子用于红细胞测定,由CUL4A转录上调。这些研究结果表明了CUL4A在原始促红细胞生成中的重要作用,并且可能对贫血和相关疾病的再生药物产生影响。

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