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造血主转录因子 MYB 的染色质占有率和靶基因。

Chromatin occupancy and target genes of the haematopoietic master transcription factor MYB.

机构信息

Department of Biosciences, University of Oslo, Blindern, PO Box 1066, 0316, Oslo, Norway.

Centre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo, 0318, Oslo, Norway.

出版信息

Sci Rep. 2021 Apr 26;11(1):9008. doi: 10.1038/s41598-021-88516-w.

Abstract

The transcription factor MYB is a master regulator in haematopoietic progenitor cells and a pioneer factor affecting differentiation and proliferation of these cells. Leukaemic transformation may be promoted by high MYB levels. Despite much accumulated molecular knowledge of MYB, we still lack a comprehensive understanding of its target genes and its chromatin action. In the present work, we performed a ChIP-seq analysis of MYB in K562 cells accompanied by detailed bioinformatics analyses. We found that MYB occupies both promoters and enhancers. Five clusters (C1-C5) were found when we classified MYB peaks according to epigenetic profiles. C1 was enriched for promoters and C2 dominated by enhancers. C2-linked genes were connected to hematopoietic specific functions and had GATA factor motifs as second in frequency. C1 had in addition to MYB-motifs a significant frequency of ETS-related motifs. Combining ChIP-seq data with RNA-seq data allowed us to identify direct MYB target genes. We also compared ChIP-seq data with digital genomic footprinting. MYB is occupying nearly a third of the super-enhancers in K562. Finally, we concluded that MYB cooperates with a subset of the other highly expressed TFs in this cell line, as expected for a master regulator.

摘要

转录因子 MYB 是造血祖细胞中的主要调节因子,也是影响这些细胞分化和增殖的先驱因子。白血病转化可能是由高 MYB 水平促进的。尽管已经积累了大量关于 MYB 的分子知识,但我们仍然缺乏对其靶基因及其染色质作用的全面了解。在本工作中,我们对 K562 细胞中的 MYB 进行了 ChIP-seq 分析,并进行了详细的生物信息学分析。我们发现 MYB 占据了启动子和增强子。当我们根据表观遗传图谱对 MYB 峰进行分类时,发现了五个簇(C1-C5)。C1 富含启动子,C2 以增强子为主。与造血特异功能相关的 C2 相关基因,其次是 GATA 因子基序。C1 除了 MYB 基序外,还具有显著频率的 ETS 相关基序。将 ChIP-seq 数据与 RNA-seq 数据相结合,使我们能够鉴定直接的 MYB 靶基因。我们还将 ChIP-seq 数据与数字基因组足迹法进行了比较。MYB 占据了 K562 中近三分之一的超级增强子。最后,我们得出结论,MYB 与该细胞系中其他高度表达的 TF 子集合作,这是作为主调控因子的预期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eeb/8076236/b545c4c7b0dc/41598_2021_88516_Fig1_HTML.jpg

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