Suppr超能文献

心肌发生分化是通过差异 mRNA 与多核糖体的关联进行精细调控的。

Cardiomyogenic differentiation is fine-tuned by differential mRNA association with polysomes.

机构信息

Basic Stem-cell Biology Laboratory, Instituto Carlos Chagas - FIOCRUZ-PR, Rua Professor Algacyr Munhoz Mader, 3775, Curitiba, PR, 81.350-010, Brazil.

Bioinformatics Unit, Institut Pasteur de Montevideo, Mataojo 2020, 11400, Montevideo, Uruguay.

出版信息

BMC Genomics. 2019 Mar 15;20(1):219. doi: 10.1186/s12864-019-5550-3.

Abstract

BACKGROUND

Cardiac cell fate specification occurs through progressive steps, and its gene expression regulation features are still being defined. There has been an increasing interest in understanding the coordination between transcription and post-transcriptional regulation during the differentiation processes. Here, we took advantage of the polysome profiling technique to isolate and high-throughput sequence ribosome-free and polysome-bound RNAs during cardiomyogenesis.

RESULTS

We showed that polysome-bound RNAs exhibit the cardiomyogenic commitment gene expression and that mesoderm-to-cardiac progenitor stages are strongly regulated. Additionally, we compared ribosome-free and polysome-bound RNAs and found that the post-transcriptional regulation vastly contributes to cardiac phenotype determination, including RNA recruitment to and dissociation from ribosomes. Moreover, we found that protein synthesis is decreased in cardiomyocytes compared to human embryonic stem-cells (hESCs), possibly due to the down-regulation of translation-related genes.

CONCLUSIONS

Our data provided a powerful tool to investigate genes potentially controlled by post-transcriptional mechanisms during the cardiac differentiation of hESC. This work could prospect fundamental tools to develop new therapy and research approaches.

摘要

背景

心脏细胞命运的决定是通过渐进的步骤发生的,其基因表达调控的特征仍在被定义。人们越来越感兴趣的是在分化过程中理解转录和转录后调控之间的协调。在这里,我们利用多核糖体分析技术,在心肌发生过程中分离和高通量地对无核糖体和多核糖体结合的 RNA 进行测序。

结果

我们表明,多核糖体结合的 RNA 表现出心肌生成的定向基因表达,而且中胚层到心脏祖细胞的阶段受到强烈的调控。此外,我们比较了无核糖体和多核糖体结合的 RNA,发现转录后调控对心脏表型的决定有很大的贡献,包括 RNA 与核糖体的招募和解离。此外,我们发现与人类胚胎干细胞(hESCs)相比,心肌细胞中的蛋白质合成减少,可能是由于与翻译相关的基因下调。

结论

我们的数据为研究 hESC 心肌分化过程中可能受转录后机制控制的基因提供了一个有力的工具。这项工作可能为开发新的治疗和研究方法提供了基本工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3686/6420765/351129f15e0a/12864_2019_5550_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验