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Ldb1 regulates carbonic anhydrase 1 during erythroid differentiation

机译:Ldb1在红系分化过程中调节碳酸酐酶1

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摘要

Carbonic anhydrase 1 (Car1), an early specific marker of the erythroid differentiation, has been used to distinguish fetal and adult erythroid cells since its production closely follows the γ- to β-globin transition, but the molecular mechanism underlying transcriptional regulation of Car1 is unclear. Here, we show that Car1 mRNA decreases significantly when erythroid differentiation is induced in MEL cells. The Ldb1 protein complex including GATA1/SCL/LMO2 binds to the Car1 promoter in uninduced cells and reduced enrichment of the complex during differentiation correlates with loss of Car1 expression. Knockdown of Ldb1 results in a reduction of Ser2 phosphorylated RNA Pol II and Cdk9 at the Car1 promoter region, suggesting that Ldb1 is required for recruitment of Pol II as well as the transcription regulator P-TEFb to enhance elongation of Car1 transcripts. Taken together, these data show that Ldb1 forms a regulatory complex to maintain Car1 expression in erythroid cells.
机译:碳酸酐酶1(Car1)是红系分化的早期特异标记,由于其产生紧密跟随γ-到β-珠蛋白的转变,因此已被用于区分胎儿和成年的红系细胞,但Car1转录调控的分子机制是不清楚。在这里,我们显示当在MEL细胞中诱导红系分化时Car1 mRNA显着降低。包含GATA1 / SCL / LMO2的Ldb1蛋白复合物与未诱导细胞中的Car1启动子结合,分化过程中复合物富集度的降低与Car1表达的丧失相关。敲低Ldb1导致Car1启动子区域的Ser2磷酸化RNA Pol II和Cdk9减少,表明Ldb1是募集Pol II以及转录调节因子P-TEFb所需的,以增强Car1转录本的延伸。综上所述,这些数据表明Ldb1形成调节复合物以维持类红细胞中Car1的表达。

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