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Zbtb14 通过抑制 zebrafish 中的表达来调节单核细胞和巨噬细胞的发育。

Zbtb14 regulates monocyte and macrophage development through inhibiting expression in zebrafish.

机构信息

Shanghai Institute of Hematology, State Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

CNRS-LIA Hematology and Cancer, Sino-French Research Center for Life Sciences and Genomics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Elife. 2022 Oct 7;11:e80760. doi: 10.7554/eLife.80760.

Abstract

Macrophages and their precursor cells, monocytes, are the first line of defense of the body against foreign pathogens and tissue damage. Although the origins of macrophages are diverse, some common transcription factors (such as PU.1) are required to ensure proper development of monocytes/macrophages. Here, we report that the deficiency of , a transcription repressor gene belonging to family, leads to an aberrant expansion of monocyte/macrophage population in zebrafish. Mechanistically, Zbtb14 functions as a negative regulator of , and SUMOylation on a conserved lysine is essential for the repression activity of Zbtb14. Moreover, a serine to phenylalanine mutation found in an acute myeloid leukemia (AML) patient could target ZBTB14 protein to autophagic degradation. Hence, is a newly identified gene implicated in both normal and malignant myelopoiesis.

摘要

巨噬细胞及其前体细胞单核细胞是机体抵御外来病原体和组织损伤的第一道防线。尽管巨噬细胞的起源多种多样,但一些常见的转录因子(如 PU.1)是确保单核细胞/巨噬细胞正常发育所必需的。在这里,我们报告说,转录抑制基因家族的一员 缺失会导致斑马鱼中单核细胞/巨噬细胞群体的异常扩增。在机制上,Zbtb14 作为 的负调控因子发挥作用,并且保守赖氨酸上的 SUMO 化对于 Zbtb14 的抑制活性是必需的。此外,在急性髓系白血病 (AML) 患者中发现的一个丝氨酸到苯丙氨酸的突变可以将 ZBTB14 蛋白靶向自噬降解。因此, 是一个新发现的基因,涉及正常和恶性髓系造血。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c08/9566859/a9dbdd2c2252/elife-80760-fig1.jpg

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