Section on Cellular and Developmental Biology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
J Exp Med. 2010 Nov 22;207(12):2543-50. doi: 10.1084/jem.20100504. Epub 2010 Nov 1.
During erythrocyte development, the nuclear cofactor Lim domain binding protein 1 (Ldb1) functions as a core subunit of multiprotein DNA binding complexes that include the transcription factors Scl and Gata-1 and the Lim-only adapter Lmo2. Scl, Gata-1, and Lmo2 are each required for erythropoiesis, suggesting that Ldb1-nucleated transcription complexes regulate key steps during erythropoiesis. We documented a requirement for Ldb1 in erythropoiesis in mice. Analysis of ldb1(-/-) embryos revealed a critical requirement for Ldb1 during primitive erythropoiesis, and conditional inactivation of ldb1 at later stages of gestation and in adult mice demonstrated that Ldb1 is continuously required for both definitive erythropoiesis and megakaryopoiesis. Down-regulation of Ldb1 in erythroblasts inhibited the expression of multiple erythroid-specific and prosurvival genes. These results represent the first unequivocal demonstration of a role for Ldb1 in erythropoiesis in vivo and establish a critical function for Ldb1-nucleated complexes in regulating the erythroid/megakaryocyte transcriptional program.
在红细胞发育过程中,核辅助因子 Lim 结构域结合蛋白 1(Ldb1)作为包含转录因子 Scl 和 Gata-1 以及 Lim 仅衔接蛋白 Lmo2 的多蛋白 DNA 结合复合物的核心亚基发挥作用。Scl、Gata-1 和 Lmo2 均是红细胞生成所必需的,这表明 Ldb1 起始的转录复合物调节红细胞生成过程中的关键步骤。我们在小鼠中记录了 Ldb1 在红细胞生成中的必要性。对 ldb1(-/-) 胚胎的分析揭示了 Ldb1 在原始红细胞生成中的关键需求,而在妊娠后期和成年小鼠中条件性失活 ldb1 表明 Ldb1 持续需要定型红细胞生成和巨核细胞生成。Ldb1 在红细胞中的下调抑制了多种红细胞特异性和生存相关基因的表达。这些结果代表了 Ldb1 在体内红细胞生成中作用的首次明确证明,并确立了 Ldb1 起始的复合物在调节红细胞/巨核细胞转录程序中的关键功能。