4.6 Article

Regulatory association of long noncoding RNAs and chromatin accessibility facilitates erythroid differentiation

期刊

BLOOD ADVANCES
卷 5, 期 23, 页码 5396-5409

出版社

ELSEVIER
DOI: 10.1182/bloodadvances.2021005167

关键词

-

资金

  1. European Union [282510-BLUEPRINT]
  2. Strategic Priority Research Program of the Chinese Academy of Sciences [XDA16010602]
  3. National Natural Science Foundation of China [82070114, 81870097, 81670109, 81700097, 81700116]
  4. National Key R&D Program of China [2017YFC0907400]

向作者/读者索取更多资源

This study uncovered the coordinated regulatory functions of lncRNAs and chromatin accessibility in erythroid differentiation by integrating RNA-seq and ATAC-seq data. Specific lncRNAs and transcription factors were identified to associate with chromatin accessibility during erythroid differentiation, highlighting their roles in the process. The study provides novel insights into the network of lncRNAs and chromatin accessibility in erythropoiesis, shedding light on the mechanisms underlying erythroid differentiation.
Erythroid differentiation is a dynamic process regulated by multiple factors, whereas the interaction between long noncoding RNAs (lncRNAs) and chromatin accessibility and its influence on erythroid differentiation remains unclear. To elucidate this interaction, we used hematopoietic stem cells, multipotent progenitor cells, common myeloid progenitor cells, megakaryocyte-erythroid progenitor cells, and erythroblasts from human cord blood as an erythroid differentiation model to explore the coordinated regulatory functions of lncRNAs and chromatin accessibility by integrating RNA-seq and ATAC-seq data. We revealed that the integrated network of chromatin accessibility and lncRNAs exhibits stage-specific changes throughout the erythroid differentiation process and that the changes at the erythroblast stage of maturation are dramatic. We identified a subset of stage-specific lncRNAs and transcription factors (TFs) that associate with chromatin accessibility during erythroid differentiation, in which lncRNAs are key regulators of terminal erythroid differentiation via an lncRNA-TF-gene network. LncRNA PCED1B-AS1 was revealed to regulate terminal erythroid differentiation by coordinating GATA1 dynamically binding to the chromatin and interacting with the cytoskeleton network during erythroid differentiation. DANCR, another lncRNA that is highly expressed at the megakaryocyte-erythroid progenitor cell stage, was verified to promote erythroid differentiation by compromising megakaryocyte differentiation and coordinating with chromatin accessibility and TFs, such as RUNX1. Overall, our results identify the associated network of lncRNAs and chromatin accessibility in erythropoiesis and provide novel insights into erythroid differentiation and abundant resources for further study.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据