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[Lin28a和Lin28b对let-7家族活性的影响]

[Effects of Lin28a and Lin28b on let-7 family activity].

作者信息

Liu Xue-Rong, Tian Wen-Hong, Dong Xiao-Yan, Wu Xiao-Zhe, Lv Jian-Xin, Wu Xiao-Bing

机构信息

Zhejiang Provincial Key Laboratory of Medical Genetics, Wenzhou Medical College, Wenzhou 325035, China.

出版信息

Bing Du Xue Bao. 2011 Nov;27(6):533-41.

Abstract

In this report, we study the effects of over-expression of Lin28a and Lin28b on let-7 family activity in HeLaS3. Firstly, we constructed pAAV2neo-Lin28a and pAAV2neo-Lin28b to express Lin28a and Lin28b, respectively. Then, pAAV2neo-Lin28a and pAAV2neo-Lin28b were transfected into HeLaS3, selected with G418 and obtained cell lines, HeLaS3/pAAV2neo-Lin28a and HeLaS3/pAAV2neo-Lin28b, to express Lin28a and Lin28b stably. Thereafter, we constructed eight plasmid vectors for detection of let-7 family activity based on pAAV2neo-Gluc-(Fluc). These vectors were further packaged into recombinant adeno-associated viral vectors (rAAV) which were used as sensors, nominated as Asensors, to detect inhibition activity of miRNA at post-transcriptional level. Subsequently, with HeLaS3 as a control, we assayed expression levels of Lin28a and Lin28b by Western blot, detected expression levels of let-7 family by QRT-PCR, and tested let-7 family activity by Asensors in HeLaS3/pAAV2neo-Lin28a and HeLaS3/pAAV2neo-Lin28b. Results demonstrated that both HeLaS3/pAAV2neo-Lin28a and HeLaS3/pAAV2neo-Lin28b could express Lin28a and Lin28b effectively. Compared with HeLaS3, the expression level of let-7 family except let-7e declined in HeLaS3/pAAV2neo-Lin28a. But declining extent among members of let-7 family was different. The let-7 family activity also decreased while the decreasing extent varied among members. Furthermore, the activity level was not consistent with its expression level for the same member in let-7 family. Compared with HeLaS3, both expression level and activity level of let-7 family in HeLaS3/ pAAV2neo-Lin28b were decreased. However, the decreasing extent of let-7 family expression changes was larger than that of HeLaS3/pAAV2neo-Lin28a while the decreasing extent of activity changes was similar. In this study, we established a method to detect and compare post-transcriptional inhibition level mediated by miRNA complementary targets. We firstly clarified the effect of Lin28a and Lin28b on let-7 family activity profile and found that this effect was not the same as that at expression level of let-7 family, suggesting that it was more comprehensive to understand miRNA regulation roles to detect both miRNA expression and activity. This paves a way for further research on mechanism of regulation of let-7 family.

摘要

在本报告中,我们研究了Lin28a和Lin28b过表达对HeLaS3细胞中let-7家族活性的影响。首先,我们构建了pAAV2neo-Lin28a和pAAV2neo-Lin28b分别用于表达Lin28a和Lin28b。然后,将pAAV2neo-Lin28a和pAAV2neo-Lin28b转染到HeLaS3细胞中,用G418进行筛选并获得细胞系HeLaS3/pAAV2neo-Lin28a和HeLaS3/pAAV2neo-Lin28b,以稳定表达Lin28a和Lin28b。此后,我们基于pAAV2neo-Gluc-(Fluc)构建了八个用于检测let-7家族活性的质粒载体。这些载体进一步包装成重组腺相关病毒载体(rAAV),用作传感器,命名为Asensors,用于在转录后水平检测miRNA的抑制活性。随后,以HeLaS3作为对照,我们通过蛋白质免疫印迹法检测HeLaS3/pAAV2neo-Lin28a和HeLaS3/pAAV2neo-Lin28b中Lin28a和Lin28b的表达水平,通过实时定量聚合酶链反应(QRT-PCR)检测let-7家族的表达水平,并使用Asensors检测let-7家族的活性。结果表明,HeLaS3/pAAV2neo-Lin28a和HeLaS3/pAAV2neo-Lin28b均能有效表达Lin28a和Lin28b。与HeLaS3相比,HeLaS3/pAAV2neo-Lin28a中除let-7e外的let-7家族表达水平下降。但let-7家族成员间的下降程度不同。let-7家族活性也降低,且各成员间降低程度各异。此外,let-7家族中同一成员的活性水平与其表达水平不一致。与HeLaS3相比,HeLaS3/pAAV2neo-Lin28b中let-7家族的表达水平和活性水平均降低。然而,let-7家族表达变化的下降程度大于HeLaS3/pAAV2neo-Lin28a,而活性变化的下降程度相似。在本研究中,我们建立了一种检测和比较由miRNA互补靶点介导的转录后抑制水平的方法。我们首先阐明了Lin28a和Lin28b对let-7家族活性谱的影响,发现这种影响与let-7家族表达水平的影响不同,这表明同时检测miRNA表达和活性对于理解miRNA调控作用更为全面。这为进一步研究let-7家族的调控机制铺平了道路。

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