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The Zebrafish moonshine Gene Encodes Transcriptional Intermediary Factor 1γ, an Essential Regulator of Hematopoiesis

机译:斑马鱼月光基因编码转录中介因子1γ,造血功能的重要调节器。

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摘要

Hematopoiesis is precisely orchestrated by lineage-specific DNA-binding proteins that regulate transcription in concert with coactivators and corepressors. Mutations in the zebrafish moonshine (mon) gene specifically disrupt both embryonic and adult hematopoiesis, resulting in severe red blood cell aplasia. We report that mon encodes the zebrafish ortholog of mammalian transcriptional intermediary factor 1γ (TIF1γ) (or TRIM33), a member of the TIF1 family of coactivators and corepressors. During development, hematopoietic progenitor cells in mon mutants fail to express normal levels of hematopoietic transcription factors, including gata1, and undergo apoptosis. Three different mon mutant alleles each encode premature stop codons, and enforced expression of wild-type tif1γ mRNA rescues embryonic hematopoiesis in homozygous mon mutants. Surprisingly, a high level of zygotic tif1γ mRNA expression delineates ventral mesoderm during hematopoietic stem cell and progenitor formation prior to gata1 expression. Transplantation studies reveal that tif1γ functions in a cell-autonomous manner during the differentiation of erythroid precursors. Studies in murine erythroid cell lines demonstrate that Tif1γ protein is localized within novel nuclear foci, and expression decreases during erythroid cell maturation. Our results establish a major role for this transcriptional intermediary factor in the differentiation of hematopoietic cells in vertebrates.
机译:造血作用是由特定于谱系的DNA结合蛋白精心编排的,这些蛋白与辅助激活剂和共加压因子协同调节转录。斑马鱼月光(mon)基因中的突变会特异性破坏胚胎和成年造血功能,导致严重的红细胞发育不良。我们报告星期一编码的哺乳动物转录中间因子1γ(TIF1γ)(或TRIM33),TIF1家族的激活因子和corepressors成员的斑马鱼直向同源物。在发育过程中,mon突变体中的造血祖细胞无法表达正常水平的造血转录因子,包括gata1,并发生凋亡。三个不同的mon突变体等位基因每个都编码过早的终止密码子,并且野生型tif1γmRNA的强制表达可以挽救纯合子mon突变体中的胚胎造血作用。出乎意料的是,高水平的合子性tif1γmRNA表达描绘了造血干细胞和gata1表达之前的祖细胞形成过程中的腹膜中胚层。移植研究表明,tif1γ在类红细胞前体分化过程中以细胞自主方式发挥作用。在鼠类红系细胞系中进行的研究表明,Tif1γ蛋白位于新型核灶中,在红系细胞成熟期间其表达降低。我们的结果建立了这种转录中介因子在脊椎动物造血细胞分化中的主要作用。

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