果蝇细胞通过分化和microRNA通路组分对小型癌症调节剂的负调控。

Turkish journal of biology = Turk biyoloji dergisi Pub Date : 2021-04-20 eCollection Date: 2021-01-01 DOI:10.3906/biy-2012-4
Sumira Malik
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引用次数: 1

摘要

果蝇模型被广泛研究用于癌症的发展。dMyc是人类MYC基因的同系物,负责细胞凋亡,其上调负责决定人类和果蝇模型中癌症生长的命运。本研究揭示了dMyc作为果蝇S2细胞中与其他蛋白和dMyc mRNA抑制的癌症的主要调节因子之一的需求。本研究报告了Argonaute 1 (AGO1)、Bag of marbles (Bam)和Brain tumor (Brat)蛋白复合物,而不是该复合物在果蝇Schneider 2细胞中抑制dMyc mRNA并促进果蝇卵巢成囊细胞分化的单个因子。这些结果显示了该复合物的显著作用,包括主分化因子Bam与其他各种分化因子Brat和microRNA通路组分AGO1,它们可能负调控dMyc mRNA,从而负调控dMyc蛋白。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Negative regulation of diminutive cancer regulator through differentiation and microRNA pathway components in Drosophila cells.

Drosophila model is intensively studied for the development of cancer. The diminutive (dMyc), a homolog of the human MYC gene, is responsible for cell- apoptosis and its upregulation is responsible for determining the fate of cancerous growth in humans and Drosophila model. This work implores the requirement of dMyc and its expression as one of the major regulator of cancer with other proteins and repression of dMyc mRNA in Drosophila S2 cells. Here we report protein complex of Argonaute 1 (AGO1), Bag of marbles (Bam), and Brain tumor (Brat) proteins and not the individual factor of this complex repression of dMyc mRNA in Drosophila Schneider 2 cells and promote differentiation in cystoblast of Drosophila ovary. These results exhibit the significant role of this complex, including master differentiation factor Bam with other various differentiation factor Brat and microRNA pathway component AGO1, which may negatively regulate dMyc mRNA and so the dMyc protein.

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