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Transcription factor and miRNA co-regulatory network reveals shared and specific regulators in the development of B cell and T cell

机译:转录因子和miRNA共同调控网络揭示了B细胞和T细胞发育过程中共享的和特定的调控因子

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摘要

The maturation process of lymphocyte was related to many blood diseases, such as lymphoma and lymphoid leukemia. Many TFs and miRNAs were separately studied in the development of B and T cells. In this study, we aim to discover the TF and miRNA co-regulation and identify key regulators in the B and T cells maturation. We obtained the candidate genes, miRNAs and TFs for each stage of their maturation, then constructed the TF-miRNA-gene feed-forward loops (FFLs) for each stage by our previous methods. Statistical test for FFLs indicated their enrichment and significance. TF-miRNA co-regulatory networks for each stage were constructed by combining their FFLs. Hub analysis revealed the key regulators in each stage, for example, MYC, STAT5A, PAX5 and miR-17 ~ 92 in the transition of pro-B cells into pre-B cells. We also identified a few common regulators and modules in two stages of B cell maturation (e.g. miR-146a/NFKB1/BCL11A) and two stages of T cell maturation (e.g. miR-20/CCND2/SORL1), as well as some shared regulators in the early stages of both B and T cell development. Our network will help to increase understanding of mature process of B and T cell, as well as the related blood diseases.
机译:淋巴细胞的成熟过程与许多血液疾病有关,例如淋巴瘤和淋巴白血病。在B细胞和T细胞的发育过程中,分别研究了许多TF和miRNA。在这项研究中,我们旨在发现TF和miRNA的共同调控,并确定B和T细胞成熟中的关键调控因子。我们获得了每个成熟阶段的候选基因,miRNA和TF,然后通过我们以前的方法为每个阶段构建了TF-miRNA基因前馈环(FFL)。对FFL的统计测试表明了其丰富性和意义。通过组合它们的FFL,构建了每个阶段的TF-miRNA共同调控网络。 Hub分析揭示了pro-B细胞向pre-B细胞过渡过程中每个阶段的关键调控因子,例如,MYC,STAT5A,PAX5和miR-17- 92。我们还在B细胞成熟的两个阶段(例如miR-146a / NFKB1 / BCL11A)和T细胞成熟的两个阶段(例如miR-20 / CCND2 / SORL1)中确定了一些常见的调节剂和模块,以及一些共享的调节剂在B和T细胞发育的早期阶段。我们的网络将有助于增进对B细胞和T细胞成熟过程以及相关血液疾病的了解。

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