Evidence map›Paper›PMID 39451156›Full record

ArticleBriefings in bioinformatics2024

Constructing the dynamic transcriptional regulatory networks to identify phenotype-specific transcription regulators.

Yang Guo, Zhiqiang Xiao

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Yang GuoSchool of Information Science and Engineering, Lanzhou University, Lanzhou 730000, China.
Zhiqiang XiaoSchool of Information Science and Engineering, Lanzhou University, Lanzhou 730000, China.

Funding

National Natural Science Foundation of China 62102173Natural Science Foundation of Gansu Province 21JR7RA509
6 · The paper itself

Abstract

The transcriptional regulatory network (TRN) is a graph framework that helps understand the complex transcriptional regulation mechanisms in the transcription process. Identifying the phenotype-specific transcription regulators is vital to reveal the functional roles of transcription elements in associating the specific phenotypes. Although many methods have been developed towards detecting the phenotype-specific transcription elements based on the static TRN in the past decade, most of them are not satisfactory for elucidating the phenotype-related functional roles of transcription regulators in multiple levels, as the dynamic characteristics of transcription regulators are usually ignored in static models. In this study, we introduce a novel framework called DTGN to identify the phenotype-specific transcription factors (TFs) and pathways by constructing dynamic TRNs. We first design a graph autoencoder model to integrate the phenotype-oriented time-series gene expression data and static TRN to learn the temporal representations of genes. Then, based on the learned temporal representations of genes, we develop a statistical method to construct a series of dynamic TRNs associated with the development of specific phenotypes. Finally, we identify the phenotype-specific TFs and pathways from the constructed dynamic TRNs. Results from multiple phenotypic datasets show that the proposed DTGN framework outperforms most existing methods in identifying phenotype-specific TFs and pathways. Our framework offers a new approach to exploring the functional roles of transcription regulators that associate with specific phenotypes in a dynamic model.

Indexed as

Gene Regulatory NetworksPhenotypeTranscription FactorsAlgorithmsComputational BiologyGene Expression RegulationHumansTranscription Factorsdynamic network constructiongraph autoencoderphenotype-specific regulatorstime-series analysistranscriptional regulatory network

Identifiers

PMID39451156
PMCPMC11503644

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.