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Gfi1 and Gfi1b act equivalently in haematopoiesis but have distinct non-overlapping functions in inner ear development

机译:Gfi1和Gfi1b在造血功能上等效但在内耳发育中具有独特的不重叠的功能

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摘要

Gfi1 is a transcriptional repressor essential for haematopoiesis and inner ear development. It shares with its paralogue Gfi1b an amino-terminal SNAG repressor domain and six carboxy-terminal zinc-finger motifs, but differs from Gfi1b in sequences separating these domains. Here, we describe two knock-in mouse models, in which the N-terminal SNAG repressor domain was mutated or in which the Gfi1 coding region was replaced by Gfi1b. Mouse mutants without an intact SNAG domain show the full phenotype of Gfi1 null mice. However, Gfi1:Gfi1b knock-in mice show almost normal pre-T-cell and neutrophil development, but lack properly formed inner ear hair cells. Hence, our findings show that an intact SNAG domain is essential for all functions of Gfi1 and that Gfi1b can replace Gfi1 functionally in haematopoiesis but, surprisingly, not in inner ear hair cell development, demonstrating that Gfi1 and Gfi1b have equivalent and domain-dependent, cell type-specific functions.
机译:Gfi1是造血和内耳发育必不可少的转录阻遏物。它与旁系同源蛋白Gfi1b共享一个氨基末端SNAG阻遏物结构域和六个羧基末端锌指基序,但在分隔这些结构域的序列上与Gfi1b不同。在这里,我们描述了两种敲入小鼠模型,其中N端SNAG阻遏物结构域发生突变,或者其中Gfi1编码区被Gfi1b取代。没有完整的SNAG域的小鼠突变体显示Gfi1空小鼠的完整表型。但是,Gfi1:Gfi1b敲入小鼠显示出几乎正常的前T细胞和嗜中性粒细胞发育,但缺少适当形成的内耳毛细胞。因此,我们的发现表明,完整的SNAG域对于Gfi1的所有功能都是必不可少的,而且Gfi1b可以在造血功能上代替Gfi1,但令人惊讶的是,在内耳毛细胞发育中却不能,这表明Gfi1和Gfi1b具有相同且依赖于域的特征,特定于细胞类型的功能。

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