Malik Sumira
Amity institute of Biotechnology, Amity University Jharkhand, Ranchi, Jharkhand India.
School of Biological Sciences and Technology, Chonnam National University the Republic of Korea.
Turk J Biol. 2021 Apr 20;45(2):180-186. doi: 10.3906/biy-2012-4. eCollection 2021.
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 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 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 Schneider 2 cells and promote differentiation in cystoblast of 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.
该模型被深入研究以用于癌症的发展。微小(dMyc),即人类MYC基因的同源物,负责细胞凋亡,其上调负责决定人类和该模型中癌性生长的命运。这项工作强调了dMyc及其表达作为癌症主要调节因子之一与其他蛋白质的关系,以及在S2细胞中dMyc mRNA的抑制。在这里,我们报告了在施耐德2细胞中,AGO1(Argonaute 1)、Bam(Bag of marbles)和Brat(Brain tumor)蛋白的蛋白质复合物,而非该复合物中单个因子对dMyc mRNA的抑制,并促进卵巢成囊母细胞的分化。这些结果表明了该复合物的重要作用,包括主要分化因子Bam与其他各种分化因子Brat以及微小RNA途径成分AGO1,它们可能对dMyc mRNA进而对dMyc蛋白产生负调控作用。