通过一系列特征动脉增强因子评估动脉基因表达的转录调控因子。

IF 6.4 1区 生物学 Q1 BIOLOGY
eLife Pub Date : 2025-01-17 DOI:10.7554/eLife.102440
Svanhild Nornes, Susann Bruche, Niharika Adak, Ian R McCracken, Sarah De Val
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引用次数: 0

摘要

动脉内皮的建立和生长需要多种基因的协调表达。然而,对这一过程的调控尚不完全清楚。在这里,我们结合转基因小鼠和斑马鱼模型的硅分析来表征与8个关键动脉识别基因(Acvrl1/Alk1、Cxcr4、Cxcl12、Efnb2、Gja4/Cx37、Gja5/Cx40、Nrp1和Unc5b)相关的动脉特异性增强子。接下来,为了阐明动脉基因转录的上游调控途径,我们研究了结合每种动脉增强因子的转录因子,并将其与非动脉内皮增强因子进行了类似的评估。这些结果发现,SOXF和ETS因子的结合在动脉和泛内皮增强细胞中都很常见,这表明两者都不足以指导动脉特异性。相反,独立于ETS基序的FOX基序在动脉增强剂中被过度代表。此外,MEF2和RBPJ的结合在动脉增强剂中丰富,但并非普遍存在,这可能与动脉内皮内的特定行为模式有关。最后,wnt相关的TCF/LEF、TGFβ/ bmp相关的SMAD1/5和SMAD2/3、剪切应力相关的KLF4或静脉富集的NR2F2没有共同或动脉特异性的特征。这组经过充分表征和体内验证的增强子现在可以为未来研究不同转录和信号通路与动脉基因表达的相互作用提供一个平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluating the transcriptional regulators of arterial gene expression via a catalogue of characterized arterial enhancers.

The establishment and growth of the arterial endothelium requires the coordinated expression of numerous genes. However, regulation of this process is not yet fully understood. Here, we combined in silico analysis with transgenic mice and zebrafish models to characterize arterial-specific enhancers associated with eight key arterial identity genes (Acvrl1/Alk1, Cxcr4, Cxcl12, Efnb2, Gja4/Cx37, Gja5/Cx40, Nrp1 and Unc5b). Next, to elucidate the regulatory pathways upstream of arterial gene transcription, we investigated the transcription factors binding each arterial enhancer compared to a similar assessment of non-arterial endothelial enhancers. These results found that binding of SOXF and ETS factors was a common occurrence at both arterial and pan-endothelial enhancers, suggesting neither are sufficient to direct arterial specificity. Conversely, FOX motifs independent of ETS motifs were over-represented at arterial enhancers. Further, MEF2 and RBPJ binding was enriched but not ubiquitous at arterial enhancers, potentially linked to specific patterns of behaviour within the arterial endothelium. Lastly, there was no shared or arterial-specific signature for WNT-associated TCF/LEF, TGFβ/BMP-associated SMAD1/5 and SMAD2/3, shear stress-associated KLF4 or venous-enriched NR2F2. This cohort of well characterized and in vivo-verified enhancers can now provide a platform for future studies into the interaction of different transcriptional and signalling pathways with arterial gene expression.

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来源期刊
eLife
eLife BIOLOGY-
CiteScore
12.90
自引率
3.90%
发文量
3122
审稿时长
17 weeks
期刊介绍: eLife is a distinguished, not-for-profit, peer-reviewed open access scientific journal that specializes in the fields of biomedical and life sciences. eLife is known for its selective publication process, which includes a variety of article types such as: Research Articles: Detailed reports of original research findings. Short Reports: Concise presentations of significant findings that do not warrant a full-length research article. Tools and Resources: Descriptions of new tools, technologies, or resources that facilitate scientific research. Research Advances: Brief reports on significant scientific advancements that have immediate implications for the field. Scientific Correspondence: Short communications that comment on or provide additional information related to published articles. Review Articles: Comprehensive overviews of a specific topic or field within the life sciences.
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