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Endothelial Foxp1 Suppresses Atherosclerosis via Modulation of Nlrp3 Inflammasome Activation.内皮细胞 Foxp1 通过调节 Nlrp3 炎性小体激活来抑制动脉粥样硬化。
Circ Res. 2019 Aug 30;125(6):590-605. doi: 10.1161/CIRCRESAHA.118.314402. Epub 2019 Jul 18.
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The Transcription Factor ETV1 Induces Atrial Remodeling and Arrhythmia.转录因子 ETV1 诱导心房重构和心律失常。
Circ Res. 2018 Aug 17;123(5):550-563. doi: 10.1161/CIRCRESAHA.118.313036.
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An integrated approach to identify critical transcription factors in the protection against hydrogen peroxide-induced oxidative stress by Danhong injection.丹红注射液通过综合方法鉴定对过氧化氢诱导的氧化应激保护作用中的关键转录因子。
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STAT3-mediated upregulation of lncRNA HOXD-AS1 as a ceRNA facilitates liver cancer metastasis by regulating SOX4.STAT3 介导的长链非编码 RNA HOXD-AS1 的上调作为 ceRNA 通过调节 SOX4 促进肝癌转移。
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Firmiana: towards a one-stop proteomic cloud platform for data processing and analysis.梧桐属:迈向一个用于数据处理和分析的一站式蛋白质组学云平台。
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Proteome-wide profiling of activated transcription factors with a concatenated tandem array of transcription factor response elements.采用串联转录因子反应元件的融合串联阵列对激活转录因子进行蛋白质组范围的分析。
Proc Natl Acad Sci U S A. 2013 Apr 23;110(17):6771-6. doi: 10.1073/pnas.1217657110. Epub 2013 Apr 3.
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[Establishment of a New-generation High-throughput Proteomic Profiling of Transcription Factor in Human Atrial Tissue].

作者信息

Wang Mang-Yuan, Huo Qiang, Yang Yi-Ning

机构信息

Clinical Medicine Postdoctoral Research Station, the First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, China.

Department of Cardiac Surgery, the First Affiliated Hospital of Xinjiang Medical University, Urumqi 830054, China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2021 Mar;52(2):274-278. doi: 10.12182/20210360208.

DOI:10.12182/20210360208
PMID:33829702
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10408923/
Abstract

OBJECTIVE

To explore for the establishment of an experimental technique for profiling transcription factors, namely transcription factor response elements (TFRE), with high throughput and efficiency using human atrial tissue.

METHODS

Postoperative right atrial tissues from 2 patients, one with preoperative atrial fibrillation and the one with no preoperative atrial fibrillation, were included in the study. The nucleus protein was extracted from the human atrial tissue, and the protein concentration was then measured. A solution with a complex formed through combining magnetic beads with concatenated tandem array of the consensus transcription factor response element DNA sequence (beads-catTFRE) was prepared, and the beads-catTFREs were then used to enrich transcription factors in the nucleoprotein extraction. SDS-PAGE electrophoresis was performed after dissociating beads-catTFRE from nucleoprotein with high temperature and high salt. The gel was then cut and faded before enzymolysis by trypsin in the gels was performed. Acetonitrile was used to extract the peptides from the gels, and the peptide solution was then dried. After that, we dissolved the peptides and performed mass spectrum tests, and the data were analyzed and processed with Firmiana one-stop proteomic analysis platform.

RESULTS

In this study, 220 and 181 transcription factors were identified in the normal right atrial tissue and the right atrial tissue with atrial fibrillation, respectively. A total of 241 transcription factors were identified in the two groups. Among the 241 transcription factors, 12 were in the top 10% of those transcription factors that were above the median expression level of the normal right atrial tissue, and 12 transcription factors were in the top 10% of those above the median expression level of the right atrial tissue with atrial fibrillation.

CONCLUSION

The high-throughput profiling method established in this study has high coverage, and the data collected can be used to support further validation studies.

摘要