Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.04.28.721260

Drying kinetics govern transcriptional and post-transcriptional reprogramming during seed maturation

Abstract

Desiccation tolerance (DT) serves as a cornerstone for seed survival and for long-term persistence in the natural environment. DT is acquired during seed development, as seeds undergo a drastic change in internal water content during maturation drying. Although the physiological effects of drying on the acquisition of DT and other seed traits have been described, the molecular mechanisms underlying these effects have not yet been fully understood. Here, we addressed this gap by submitting maturing seeds of Arabidopsis thaliana L. to three different drying regimes - fast drying (FD), slow drying (SD), and a combination of both (SDFD) and studying physiological, transcriptional, and post-transcriptional responses. We found that SD not only accelerated DT acquisition but also seed maturation. Each drying regime showed a distinct transcriptional signature, with SD and SDFD showing greater global gene downregulation compared to FD. This downregulation appeared to be crucial for establishing DT in developing seeds. Interestingly, FD triggered a specific defense-related transcriptional response that was detrimental to seed longevity. Using an abscisic acid deficient mutant, we found that most of the drying-mediated transcriptional changes were largely independent of the wild-type ABA levels. On a post-transcriptional level, SD led to a major turnover of mRNA populations undergoing co-translational mRNA decay (CTRD) and promoted CTRD of stress-related genes. Overall, our study provides fundamental insights into the mechanisms by which seeds perceive and respond to drying, advancing our basic understanding of the molecular regulation of DT and seed maturation. Significance StatementSeed maturation is a critical phase of the plant life cycle when seeds acquire desiccation tolerance (DT) required for long-term storage. Drying rate, together with abscisic acid (ABA), has been implicated in this process, but whether seed development actively responds to different drying rates and how such responses are regulated has remained unclear. Here, we show that maturing seeds sense and respond to different drying regimes through distinct molecular programs, with slow drying triggering coordinated transcriptional and post-transcriptional reprogramming associated with enhanced DT. This response occurs partly independent of wild-type ABA levels, revealing drying rate as a developmental signal acting alongside hormonal regulation to direct seed maturation. These findings provide a framework for improving drying strategies and identifying molecular markers of seed quality.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Sami, A. A., Willems, L. A. J., Abdulroheem, L., Carpentier, M.-C., Merret, R., Bentsink, L., Artur, M. A. S.. 2026-05-01. Drying kinetics govern transcriptional and post-transcriptional reprogramming during seed maturation. https://doi.org/10.64898/2026.04.28.721260

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Molecular and phytochemical investigation of medicinal Rhododendron spp. in the Qinghai-Xizang Plateau: the botanical sources of the traditional Tibetan medicine "Tale"

The Qinghai-Xizang Plateau in China is a hotspot for Rhododendron species, with approximately 400 species distributed across the region. Various Rhododendron species in this area have been used medicinally in traditional Tibetan medicine for a long time and are collectively referred to as "Tale." Furthermore, "Tale" is classified as "Talegabao" or "Talenabao," depending on the species. These two types of medicine have similar but distinct properties, and "Talenabao" is usually used as an alternative to "Talegabao." However, differences in their phytochemical compositions and methods for discriminating between them have not been examined. To solve these problems limited the use of "Tale" medicines, 46 plant specimens belonging to nine Rhododendron species were collected from the Qinghai-Xizang Plateau. Molecular methods based on the internal transcribed spacer 2 (ITS2) region of nuclear DNA and psbA-trnH regions of chloroplast DNA were applied to these samples. In addition, 10 flavonoid compounds were quantitatively determined by HPLC. The results indicated psbA-trnH region successfully distinguished the species used as "Talegabao" or "Talenabao," whereas ITS2 failed to distinguish them because of its high degree of conservation. All 10 compounds were detected in all samples. However, the species used as "Talegabao" had more than twice the total content of the 10 flavonoid compounds observed in the species used as "Talenabao." Moreover, differences in the contents of certain compounds among species were detected, indicating potential chemical markers for the quality evaluation of "Tale" medicines. "Talegabao" is the first choice among "Tale" medicines. "Talenabao" can be used as an alternative to "Talegabao"; however, the appropriate dose requires further discussion in practical use. The psbA-trnH region is recommended as a DNA barcode for distinguishing between these two types of medicines.

plant biology↗

Accessory B Chromosomes Alter Chromatin Accessibility and Gene Expression in Maize Pollen Nuclei

B chromosomes in maize (Zea mays L.) are supernumerary, nonessential chromosomes that exhibit non-Mendelian inheritance through chromosome drive. During the second pollen mitosis, they undergo nondisjunction, resulting in their preferential transmission via B-containing sperm cells. Although their transmission mechanisms have been extensively characterized, the effects on chromatin organization and transcriptional regulation in gametophytic cells remain poorly understood. Here, we combined flow cytometric sorting of pollen nuclei with an assay for transposase-accessible chromatin sequencing (ATAC-seq) and RNA sequencing (RNA-seq) to investigate the impact of B chromosomes on chromatin accessibility and gene expression in mature maize pollen. Using pollen nuclei isolated from a maize inbred line B73 carrying zero and two B chromosomes, we generated high-purity datasets suitable for integrated chromatin and transcriptomic analyses. We identified extensive chromatin accessibility and transcriptional activity at B-chromosome loci. Importantly, the presence of B chromosomes was also associated with altered chromatin accessibility and gene expression on the standard A chromosomes, revealing regulatory effects extending beyond the B chromosome itself. Together, these findings contribute to a broader understanding of effects of selfish genetic elements in plants.

plant biology↗

Melanoidins Suppress Cucumber and Tomato Diseases Incited by Pathogens that are Oomycetes, Bacteria and a Virus

We recently reported that solutions of the nitrogenous compounds melanoidins (M), that are formed during the final stages of the Maillard Reaction, are inducers of plant resistance (Elad et al. 2026). M promoted immunity and induced disease resistance through an effect on the transcriptome, primarily through the salicylic acid pathway. Here we tested the effect of M on plant diseases that are caused by Oomycetes, bacteria and a tobamovirus. Drench and spray of M suppressed Pythium aphanidermatum damping off in cucumber, cucumber downy mildew (Pseudoperonospera cubensis), tomato late blight (Phytophthora infestans), bacterial speck (Pseudomonas syringae pv. tomato), bacterial canker (Clavibacter michiganensis subsp. michiganensis) and the Tobamovirus Tomato brown rugose fruit virus (ToBRFV) in tomato. In various experiments control was achieved by concentrations of 0.03 and 0.1% and on older and younger leaves and even in long term experiments where the M was applied for ca 11 weeks. It can be concluded that the disease resistance inducer M can suppress soilborne and foliar diseases that are caused by Oomycetes, bacteria and a virus of the genus Tobamovirus, in addition to the fungal pathogen Botrytis cinerea reported earlier.

plant biology↗