Buying time - increasing yield potential in wheat by extending stem elongation duration

Kronenberg, L.; Gonzalez-Navarro, O. E.; Collier, S.; Chhetry, M.; Tailby, P.; Leverington-Waite, M.; Wingen, L. U.; Griffiths, S.

doi:10.1101/2025.04.28.650957

bioRxiv · 10.1101/2025.04.28.650957

Buying time - increasing yield potential in wheat by extending stem elongation duration

Kronenberg, L.·Gonzalez-Navarro, O. E.·Collier, S.·Chhetry, M.·Tailby, P.·Leverington-Waite, M.·Wingen, L. U.·Griffiths, S.

View original source ↗Export metadata ↓

Abstract

Extending the duration of the stem elongation (SE) phase between terminal spikelet (TS) and anthesis has often been proposed as an avenue to increase wheat yield. However, accurate determination of TS is labour intensive, and existing evidence is often based on a limited number of genotypes observed under controlled conditions. Here, a Buster x Charger population comprising 108 doubled haploid lines was grown across four year-sites under UK field conditions. TS was recorded through meristem dissection and SE duration was measured as the time between TS and ear emergence (EE). Mixed model analysis across year-sites revealed high heritabilities (H2yield = 0.66, H2TS = 0.93, H2SE = 0.89, H2EE = 0.95) and strong genetic correlations between yield and the phenology traits SE and EE (rg = 0.56 and rg = 0.6, respectively). While SE duration was mainly driven by EE, independent QTL for TS suggest that SE could be modified without affecting EE. The positive effect of SE duration on yield was attributed to increased grain number per area as well as increased grain weight, through independent QTL. Although validation in broader genetic backgrounds is needed, these QTL may offer opportunities for further yield increase in a physiological breeding framework. HighlightsO_LILonger stem elongation duration increases grain number. C_LIO_LILonger stem elongation duration increases grain weight. C_LIO_LIIndependent QTL suggest the timing of stem elongation as well as its effect on yield components may be independently selectable. C_LI

Explore related subjects

genetics Preprint

Keep this discovery

Explore connections, maps & timelines

BibTeX RIS

Kronenberg, L., Gonzalez-Navarro, O. E., Collier, S., Chhetry, M., Tailby, P., Leverington-Waite, M., Wingen, L. U., Griffiths, S.. 2025-05-01. Buying time - increasing yield potential in wheat by extending stem elongation duration. https://doi.org/10.1101/2025.04.28.650957

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

KEEP EXPLORING

Related preprints

bioRxiv2026

OPA1 controls mitochondrial dysfunction-driven liver fibrosis in MASLD

Progressive hepatic fibrosis is the principal determinant of morbidity and mortality in metabolic dysfunction-associated steatotic liver disease and steatohepatitis (MASLD/MASH). Mitochondrial dysfunction is a hallmark of MASH, and the release of mitochondrial damage-associated molecular patterns (mito-DAMPs) from injured hepatocytes can promote fibrosis. However, how mitochondrial dynamics and quality control shape the fibrotic response in MASLD/MASH remains unclear. Here, through large-scale genomic analyses of mitochondrial genes governing mitophagy, fusion and fission in human MASLD, with a power-equivalent sample size of approximately 700,000 individuals, we identify a strong association between hepatic fibrosis and the mitochondrial fusion factor dynamin-like GTPase optic atrophy 1 (OPA1). OPA1 transcripts and protein abundance in the liver epithelium were progressively dysregulated with advancing fibrosis. In mice, hepatocyte-specific OPA1 loss alone was sufficient to induce hepatic stellate cell activation and fibrosis in zone 3, promoted the release of mito-DAMPs into the circulation and exacerbated fibrosis in experimental MASH. These findings identify OPA1 as a central regulator of the hepatic fibrotic response and connect defective mitochondrial homeostasis to mito-DAMP release, hepatic stellate cell activation and fibrosis in MASLD.

genetics↗

bioRxiv2026

Temporal control of mitochondrial mutagenesis reveals the fate of mtDNA mutations with age

Mutations in the mitochondrial genome (mtDNA) play a critical role in the aging process and a wide variety of age-related diseases. However, it remains unclear when the mutations that drive physiological decline arise. To answer this question, we generated a new mouse model in which mitochondrial mutagenesis can be confined to a defined window of time. Surprisingly, we found that mutations that arise during the first two months of life are sufficient to drive a wide variety of age-related pathologies, and that the severity of this pathology is broadly regulated by distinct, tissue-specific selective pressures that control the fate of mtDNA mutations with age. Further, we found that selection against deleterious variants can be modulated by manipulation of mitochondrial fusion in vitro and in vivo. These observations raise the possibility that in some tissues, the pace of aging is pre-determined by events that occur early in life and that interventions targeting mitochondrial fusion may be able to slow down or reverse the expansion of these pathogenic variants. These results carry far-reaching implications for strategies aimed at preventing or delaying age-related decline.

genetics↗

bioRxiv2026

Innate immune stress pathway activation underlies heterochromatin dysfunction pathology

Heterochromatin loss disrupts nuclear architecture, gene regulation and repetitive element silencing, and is associated with diverse human diseases. However, mechanisms linking heterochromatin dysfunction to pathological phenotypes remain unclear. Using genetic interaction screening and genomic analyses in C. elegans, we identify secondary activation of the Intracellular Pathogen Response (IPR), an innate immune stress pathway, as a major contributor to heterochromatin mutant phenotypes. Constitutive IPR activation phenocopies slow growth and indirect transcriptional changes observed in these mutants. Depletion of genetic enhancers further increased, whereas suppressor RNAi attenuated IPR activation, with direct heterochromatin targets remaining substantially deregulated. Notably, many suppressors encode active chromatin components, and mild reduction of RNA polymerase II activity ameliorates growth defects in C. elegans HP1 mutants and human HP1-deficient cells. Our findings reveal secondary stress response activation as an important mechanism linking heterochromatin dysfunction to pathology and identify transcriptional dampening as a potential therapeutic strategy for mitigating these effects.

genetics↗