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Chicken gga-miR-181a targets MYBL1 and shows an inhibitory effect on proliferation of Marek's disease virus-transformed lymphoid cell line

机译:鸡gga-miR-181a靶向MYBL1,对马立克氏病病毒转化的淋巴样细胞系的增殖具有抑制作用

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Marek's disease (MD), caused by Marek's disease virus (MDV), is a lymphoproliferative neoplastic disease of chickens and is characterized by MD lymphoma in multiple visceral organs of chicken. It causes great damage to poultry health. Recently, miRNA has been reported to be involved in Marek's disease lymphomagenesis. Our previous study showed that ggamiR-181a was downregulated in MDV-induced lymphoma, and its target gene, v-myb myeloblastosis viral oncogene homolog-like 1 (MYBL1), was predicted. In this study, the interaction between gga-miR-181a and MYBL1 was further verified by detecting protein expression levels of MYBL1 after transfecting miR-181a mimic into MD lymphoma cell line, MSB1. The result showed that protein level of MYBL1 was lower in gga-miR-181a mimic transfecting group than that in the negative control group at 96 h post transfection, which indicated that MYBL1 was a target gene of gga-miR-181a. Additionally, we found that the expression of MYBL1 was higher in MDV-infected samples than that in non-infected controls, which agreed with the proposition that miRNA showed a negatively correlated expression pattern with its target gene. We observed the inhibitory effect of gga-miR-181a on MSB1 cell proliferation. Collectively, the aberrant expression of gga-miR-181a and MYBL1 in MD lymphoma suggested that they might be involved in MD tumor transformation and played important roles.
机译:由马立克氏病病毒(MDV)引起的马立克氏病(MD)是鸡的淋巴增生性肿瘤病,其特征是在鸡的多个内脏器官中均存在MD淋巴瘤。它对家禽健康造成极大损害。最近,据报道,miRNA参与了马立克氏病淋巴瘤的发生。我们先前的研究表明,ggamiR-181a在MDV诱导的淋巴瘤中被下调,并预测了其靶标基因v-myb成纤维细胞病病毒致癌基因同源物1(MYBL1)。在这项研究中,通过将miR-181a模拟物转染到MD淋巴瘤细胞系MSB1中后,通过检测MYBL1的蛋白表达水平来进一步验证gga-miR-181a与MYBL1之间的相互作用。结果显示,转染后96 h,gga-miR-181a模拟转染组MYBL1蛋白水平低于阴性对照组,表明MYBL1是gga-miR-181a的靶基因。此外,我们发现在MDV感染的样品中,MYBL1的表达高于未感染的对照,这与miRNA与其目标基因呈负相关表达模式的主张相符。我们观察到gga-miR-181a对MSB1细胞增殖的抑制作用。总的来说,gga-miR-181a和MYBL1在MD淋巴瘤中的异常表达提示它们可能参与了MD肿瘤的转化并发挥了重要作用。

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