DeepEvo

<p dir="ltr">The identification of adaptively driven genes underlying human evolutionary traits remains a key challenge in evolutionary genomics. Here we present DeepEvo, an interpretable Siamese neural network that predicts cross-species expression differences from orthologous seque...

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Egile nagusia: Juntian Qi (22578974) (author)
Argitaratua: 2025
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author Juntian Qi (22578974)
author_facet Juntian Qi (22578974)
author_role author
dc.creator.none.fl_str_mv Juntian Qi (22578974)
dc.date.none.fl_str_mv 2025-11-25T05:34:48Z
dc.identifier.none.fl_str_mv 10.6084/m9.figshare.30581129.v2
dc.relation.none.fl_str_mv https://figshare.com/articles/dataset/DeepEvo/30581129
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Bioinformatic methods development
Genomics and transcriptomics
Sequence analysis
Human evolution
Adaptively driven genes
Cis-regulatory elements
Siamese neural networks
dc.title.none.fl_str_mv DeepEvo
dc.type.none.fl_str_mv Dataset
info:eu-repo/semantics/publishedVersion
dataset
description <p dir="ltr">The identification of adaptively driven genes underlying human evolutionary traits remains a key challenge in evolutionary genomics. Here we present DeepEvo, an interpretable Siamese neural network that predicts cross-species expression differences from orthologous sequences while pinpointing evolutionary regulatory variants. DeepEvo outperforms existing methods in cross-species modeling, with validation through documented annotations and single-base perturbation assays (MPRA/Perturb-seq). We discover that unlike population-level variations that predominantly disrupt existing regulatory motifs, evolutionary regulatory variants frequently enhance existing motifs over longer timescales. These variants are enriched in disease-associated regions, indicating their shared functions underlying human evolution and disease. Furthermore, analysis of their combinatorial cis-regulation revealed an ‘additive effect’ model. Within this framework, genes can maintain global stability through compensatory changes, while simultaneously achieving precise, cell-type-specific expression changes. This insight led to a ‘concerted drive’ strategy, prioritizing four adaptively driven genes that function across multiple systems, based on coordinated pushes from multiple evolutionary regulatory elements. As validation, we focused on PRKD2, upregulated in humans through concordant cis-regulatory changes. PRKD2-depleted rhesus macaques exhibited multi-system alterations—including reduced neuronal activity, decreased dendritic complexity, altered functional connectivity of brain, elevated insulin levels and lymphocyte counts—recapitulating key human-rhesus phenotypic differences. Our framework deciphers the cis-regulatory grammar of human transcriptome evolution and provides an effective strategy for identifying adaptively driven genes, generalizable to other cross-species comparisons.</p>
eu_rights_str_mv openAccess
id Manara_4873c6450a2fcc6695b810949ffbdb36
identifier_str_mv 10.6084/m9.figshare.30581129.v2
network_acronym_str Manara
network_name_str ManaraRepo
oai_identifier_str oai:figshare.com:article/30581129
publishDate 2025
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
rights_invalid_str_mv CC BY 4.0
spelling DeepEvoJuntian Qi (22578974)Bioinformatic methods developmentGenomics and transcriptomicsSequence analysisHuman evolutionAdaptively driven genesCis-regulatory elementsSiamese neural networks<p dir="ltr">The identification of adaptively driven genes underlying human evolutionary traits remains a key challenge in evolutionary genomics. Here we present DeepEvo, an interpretable Siamese neural network that predicts cross-species expression differences from orthologous sequences while pinpointing evolutionary regulatory variants. DeepEvo outperforms existing methods in cross-species modeling, with validation through documented annotations and single-base perturbation assays (MPRA/Perturb-seq). We discover that unlike population-level variations that predominantly disrupt existing regulatory motifs, evolutionary regulatory variants frequently enhance existing motifs over longer timescales. These variants are enriched in disease-associated regions, indicating their shared functions underlying human evolution and disease. Furthermore, analysis of their combinatorial cis-regulation revealed an ‘additive effect’ model. Within this framework, genes can maintain global stability through compensatory changes, while simultaneously achieving precise, cell-type-specific expression changes. This insight led to a ‘concerted drive’ strategy, prioritizing four adaptively driven genes that function across multiple systems, based on coordinated pushes from multiple evolutionary regulatory elements. As validation, we focused on PRKD2, upregulated in humans through concordant cis-regulatory changes. PRKD2-depleted rhesus macaques exhibited multi-system alterations—including reduced neuronal activity, decreased dendritic complexity, altered functional connectivity of brain, elevated insulin levels and lymphocyte counts—recapitulating key human-rhesus phenotypic differences. Our framework deciphers the cis-regulatory grammar of human transcriptome evolution and provides an effective strategy for identifying adaptively driven genes, generalizable to other cross-species comparisons.</p>2025-11-25T05:34:48ZDatasetinfo:eu-repo/semantics/publishedVersiondataset10.6084/m9.figshare.30581129.v2https://figshare.com/articles/dataset/DeepEvo/30581129CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/305811292025-11-25T05:34:48Z
spellingShingle DeepEvo
Juntian Qi (22578974)
Bioinformatic methods development
Genomics and transcriptomics
Sequence analysis
Human evolution
Adaptively driven genes
Cis-regulatory elements
Siamese neural networks
status_str publishedVersion
title DeepEvo
title_full DeepEvo
title_fullStr DeepEvo
title_full_unstemmed DeepEvo
title_short DeepEvo
title_sort DeepEvo
topic Bioinformatic methods development
Genomics and transcriptomics
Sequence analysis
Human evolution
Adaptively driven genes
Cis-regulatory elements
Siamese neural networks