Evidence map›Paper›PMID 41280085›Full record

ArticlebioRxiv : the preprint server for biology2025

Natural variation in regulatory code revealed through Bayesian analysis of plant pan-genomes and pan-transcriptomes.

Wei Wei, Xing Wu, Chandler A Sutherland, Yuting Lin, China Lunde, Moises Exposito-Alonso, Ksenia Krasileva

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Wei WeiDepartment of Plant and Microbial Biology, University of California Berkeley, Berkeley, CA 94720, USA.ORCID 0000-0002-1337-5253
Xing WuDepartment of Integrative Biology, University of California Berkeley, Berkeley, CA 94720, USA.ORCID 0000-0002-8579-7025
Chandler A SutherlandDepartment of Plant and Microbial Biology, University of California Berkeley, Berkeley, CA 94720, USA.ORCID 0000-0001-5840-7661
Yuting LinDepartment of Plant and Microbial Biology, University of California Berkeley, Berkeley, CA 94720, USA.
China LundeDepartment of Plant and Microbial Biology, University of California Berkeley, Berkeley, CA 94720, USA.ORCID 0000-0003-0513-9709
Moises Exposito-AlonsoDepartment of Integrative Biology, University of California Berkeley, Berkeley, CA 94720, USA.ORCID 0000-0001-5711-0700
Ksenia KrasilevaDepartment of Plant and Microbial Biology, University of California Berkeley, Berkeley, CA 94720, USA.ORCID 0000-0002-1679-0700

Funding

Cross-kingdom health: evolution of innate immune receptors and their targetsDP2AT011967 · NCCIH · UNIVERSITY OF CALIFORNIA BERKELEY · PI KRASILEVA, KSENIA V · 2021 to 2024
$2.2M
NCCIH NIH HHS DP2 AT011967
6 · The paper itself

Abstract

Understanding the genetic code of cis-regulatory elements (CREs) is essential for engineering gene expression and modulating agronomic traits in crops. In plants, CREs underlying rapid evolution of gene expression often overlap with structural variation in promoters, making them undetectable using single-reference genomes. Here, we develop K-PROB (K-mer-based in silico PROmoter Bashing), a computational tool that learns from intraspecies promoter sequence and gene expression variation in pan-genomes and pan-transcriptomes to identify CREs controlling gene expression. K-PROB deploys a k-mer-based Bayesian variable selection framework to prioritize causal variable identification. We demonstrate the effectiveness of our approach in maize and soybean, two staple crops species. Applying K-PROB to genes with the most highly variable promoter sequences and the most diverse patterns of expression, such as nucleotide-binding leucine-rich repeat receptors, we identified k-mers enriched for bona fide transcription factor binding sequences, and overlapping with open chromatin regions and DAP-seq binding sites. Notably, multiple significant k-mers are located within presence/absence structural variants, highlighting structural variation in promoters as key drivers of transcriptional diversity of highly variable genes. We further validated the regulatory effects of identified k-mers on gene expression using luciferase reporter assays. Our results showcase a high-throughput and pangenomic approach for probing natural intraspecies cis-regulatory diversity, discovering new causative cis-elements, and facilitating future expression engineering across plant species.

Indexed as

Biophysics and Computational Biologyk-mermachine learningnatural variationpangenomicsPlant Biologytranscriptional regulation

Identifiers

PMID41280085
PMCPMC12636352

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.