In silico screening system based on a transcription factors regulatory network only using transcriptomic data

In this study, we developed a method to identify core transcription factors (TFs) involved in differentiation using only comprehensive gene analysis. The theory of in silico screening using TFs regulatory network analysis (ISNA) required the following requirements: (1) estimating promoter regions, (2) constructing TFs regulatory network (TRN) relationships using the nucleotide sequence information in the promoters and score matrices derived from TF consensus sequences, and (3) identifying candidate core TFs by determining dissociation constants (Kd values) within the relationships of TRN. ISNA demonstrated the ability to predict the core TFs involved in the endothelial-to-mesenchymal transition of human umbilical vein endothelial cell (HUVEC) and the differentiation of human embryonic stem cells into mesodermal cells. Using ISNA, we identified HMGA2 as a novel core TF in uterine epithelium. Notably, HMGA2 expression was predominantly detected in uterine epithelium, where it regulated cell proliferation in response to estrogen. These findings highlight ISNA's potential to identify core TFs based on transcriptomic data.

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Publication Details

Journal
PLoS ONE
Published
2025-04-07
DOI
https://doi.org/10.1371/journal.pone.0319971
Primary Topic
Cancer-related molecular mechanisms research
Type
article
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0.00
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article

In silico screening system based on a transcription factors regulatory network only using transcriptomic data

Tomomi Sato, Kazuo Harada, Yasuhiro Tomooka, Tadaaki Nakajima
PLoS ONE
Cancer-related molecular mechanisms research
article

In silico screening system based on a transcription factors regulatory network only using transcriptomic data

Tomomi Sato, Kazuo Harada, Yasuhiro Tomooka, Tadaaki Nakajima
article en

Abstract

In this study, we developed a method to identify core transcription factors (TFs) involved in differentiation using only comprehensive gene analysis. The theory of in silico screening using TFs regulatory network analysis (ISNA) required the following requirements: (1) estimating promoter regions, (2) constructing TFs regulatory network (TRN) relationships using the nucleotide sequence information in the promoters and score matrices derived from TF consensus sequences, and (3) identifying candidate core TFs by determining dissociation constants (Kd values) within the relationships of TRN. ISNA demonstrated the ability to predict the core TFs involved in the endothelial-to-mesenchymal transition of human umbilical vein endothelial cell (HUVEC) and the differentiation of human embryonic stem cells into mesodermal cells. Using ISNA, we identified HMGA2 as a novel core TF in uterine epithelium. Notably, HMGA2 expression was predominantly detected in uterine epithelium, where it regulated cell proliferation in response to estrogen. These findings highlight ISNA's potential to identify core TFs based on transcriptomic data.

PLoS ONEVol. 20(4)
Tokyo University of Science (JP), Yokohama City University (JP)
Openalex Percentile: Top 92%
Cancer-related molecular mechanisms research
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