[Leukemia-associated gene ASXL1 involved in paraspeckle formation].

Keita Yamamoto
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Abstract

Somatic mutations in the ASXL1 gene are commonly observed in myeloid neoplasms. Pathogenic ASXL1 mutations induce the expression of C-terminally truncated mutant ASXL1 protein. We have shown that wild-type ASXL1 is a phase-separating protein involved in the formation of paraspeckles, one of the best known membraneless organelles (MLOs). Mutant ASXL1 lacks the intrinsically disordered region, which is important for phase separation and fails to support paraspeckle formation. Additionally, paraspeckles are disrupted in hematopoietic cells derived from ASXL1-MT knockin mice. The disruption of paraspeckles in hematopoietic cells results in a dysfunction of the hematopoietic reconstitution capacity. Therefore, this review presents our findings and summarizes the knowledge of phase separation and MLOs as a hot topic in cell biology.

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[白血病相关基因ASXL1参与副斑形成]。
ASXL1基因的体细胞突变常见于髓系肿瘤。致病性ASXL1突变诱导c端截断突变体ASXL1蛋白的表达。我们已经证明,野生型ASXL1是一种参与副斑形成的相分离蛋白,副斑是最著名的无膜细胞器(MLOs)之一。突变型ASXL1缺乏对相分离很重要的内在无序区,不能支持副散斑的形成。此外,ASXL1-MT敲入小鼠的造血细胞中的副斑被破坏。造血细胞副斑的破坏导致造血重建能力的功能障碍。因此,本文综述了我们的研究结果,并对相分离和MLOs作为细胞生物学的一个热点问题进行了总结。
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