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Ldb1在红细胞分化过程中调节碳酸酐酶1。

Ldb1 regulates carbonic anhydrase 1 during erythroid differentiation.

作者信息

Song Sang-Hyun, Kim Aeri, Dale Ryan, Dean Ann

机构信息

Cancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.

出版信息

Biochim Biophys Acta. 2012 Aug;1819(8):885-91. doi: 10.1016/j.bbagrm.2012.05.001. Epub 2012 May 18.

Abstract

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.

摘要

碳酸酐酶1(Car1)是红系分化的早期特异性标志物,由于其产生与γ-珠蛋白向β-珠蛋白的转变密切相关,因此一直被用于区分胎儿和成人红系细胞,但Car1转录调控的分子机制尚不清楚。在此,我们表明,当在MEL细胞中诱导红系分化时,Car1 mRNA显著减少。包括GATA1/SCL/LMO2在内的Ldb1蛋白复合物在未诱导的细胞中与Car1启动子结合,分化过程中该复合物富集的减少与Car1表达的丧失相关。敲低Ldb1会导致Car1启动子区域的Ser2磷酸化RNA聚合酶II和Cdk9减少,这表明Ldb1是招募Pol II以及转录调节因子P-TEFb以增强Car1转录本延伸所必需的。综上所述,这些数据表明Ldb1形成一个调节复合物以维持红系细胞中Car1的表达。

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