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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表达促进斑马鱼原始红细胞生成

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摘要

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是Cullin家族中密切相关的成员,可以各自组装Cullin-RING E3连接酶复合物(Cullin-RING连接酶4A或4B,CRL4A或CRL4B),并参与多种生物学过程。以前,我们显示斑马鱼cul4a(而非cul4b)对于心脏和胸鳍的发育至关重要。在这里,我们已经确定cul4a是斑马鱼胚胎发育中原始红细胞生成的关键调节因子。 cul4a的耗尽由于抑制了红系分化而导致红系细胞显着减少。在cul4a缺陷型胚胎中,早期造血调节基因(包括scl,lmo2和gata1)的转录水平显着降低。从机制上讲,我们证明了scl和gata1,即原始血细胞生成的红细胞确定性的中央调节因子,被cul4a转录上调。这些发现证明了cul4a在原始红细胞生成中的重要作用,并可能对贫血和相关疾病的再生医学产生影响。

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