Evidence map›Paper›PMID 38813828›Full record

ArticleNucleic acids research2024

The developmental and evolutionary characteristics of transcription factor binding site clustered regions based on an explainable machine learning model.

Zhangyi Ouyang, Feng Liu, Wanying Li, Junting Wang, Bijia Chen, Yang Zheng, Yaru Li, Huan Tao, Xiang Xu, Cheng Li and 4 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Zhangyi OuyangAcademy of Military Medical Sciences, Beijing 100850, China.ORCID 0000-0002-9905-9832
Feng LiuCollege of Medical Informatics, Chongqing Medical University, Chongqing 400016, China.ORCID 0000-0001-9410-676X
Wanying LiAcademy of Military Medical Sciences, Beijing 100850, China.
Junting WangAcademy of Military Medical Sciences, Beijing 100850, China.
Bijia ChenAcademy of Military Medical Sciences, Beijing 100850, China.
Yang ZhengAcademy of Military Medical Sciences, Beijing 100850, China.
Yaru LiAcademy of Military Medical Sciences, Beijing 100850, China.
Huan TaoAcademy of Military Medical Sciences, Beijing 100850, China.
Xiang XuAcademy of Military Medical Sciences, Beijing 100850, China.
Cheng LiCenter for Bioinformatics, School of Life Sciences, Center for Statistical Science, Peking University, Beijing 100871, China.
Yuwen CongAcademy of Military Medical Sciences, Beijing 100850, China.
Hao LiAcademy of Military Medical Sciences, Beijing 100850, China.
Xiaochen BoAcademy of Military Medical Sciences, Beijing 100850, China.ORCID 0000-0003-1911-7922
Hebing ChenAcademy of Military Medical Sciences, Beijing 100850, China.ORCID 0000-0003-4102-356X

Funding

Beijing Natural Science Foundation 5232025Beijing Nova Program of Science and Technology 20220484198Chongqing Natural Science Foundation of China CSTB2022NSCQ-MSX1059National Natural Science Foundation of China 62173338
6 · The paper itself

Abstract

Gene expression is temporally and spatially regulated by the interaction of transcription factors (TFs) and cis-regulatory elements (CREs). The uneven distribution of TF binding sites across the genome poses challenges in understanding how this distribution evolves to regulate spatio-temporal gene expression and consequent heritable phenotypic variation. In this study, chromatin accessibility profiles and gene expression profiles were collected from several species including mammals (human, mouse, bovine), fish (zebrafish and medaka), and chicken. Transcription factor binding sites clustered regions (TFCRs) at different embryonic stages were characterized to investigate regulatory evolution. The study revealed dynamic changes in TFCR distribution during embryonic development and species evolution. The synchronization between TFCR complexity and gene expression was assessed across species using RegulatoryScore. Additionally, an explainable machine learning model highlighted the importance of the distance between TFCR and promoter in the coordinated regulation of TFCRs on gene expression. Our results revealed the developmental and evolutionary dynamics of TFCRs during embryonic development from fish, chicken to mammals. These data provide valuable resources for exploring the relationship between transcriptional regulation and phenotypic differences during embryonic development.

Indexed as

Evolution, MolecularGene Expression Regulation, DevelopmentalMachine LearningTranscription FactorsAnimalsBinding SitesCattleChickensChromatinEmbryonic DevelopmentHumansMiceOryziasPromoter Regions, GeneticChromatinTranscription Factors

Identifiers

PMID38813828
PMCPMC11260490

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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 Socratic graph.