ArticleTAG. Theoretical and applied genetics. Theoretische und angewandte Genetik2025
Genetic and transcriptomic identification of WPG1 controlling nitrogen allocation-related leaf chlorisis and premature senescence in wheat.
Article in TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
14 authors.
Funding
Abstract
Leaf senescence is a turning point for grain development and closely related to yield and grain quality. Fine-tuning leaf senescence could be a vital strategy for yield improvement. However, our knowledge of the regulatory genes of leaf senescence is limited in wheat. In this study, we identified a methanesulfonate (EMS) mutant, wheat pale green 1 (wpg1), exhibiting obvious leaf chlorisis and premature senescence (PS) since the jointing stage. The chloroplast structure of the chlorisis leaf of wpg1 seemed intact, whereas its chlorophyll content was significantly decreased compared to the wild type (WT). The content of nitrogen (N), the core element for chlorophyll, was much lower in leaves of wpg1 than in WT. The spatio-temporal pattern analysis of nitrogen content further indicated accelerated N allocation from vegetation tissues to spike in wpg1, resulting in a significant decrease in nitrogen content in leaves, but a substantial increase in grains compared to WT. Genetic analysis showed that leaf chlorisis and PS is controlled by a single dominant locus, designated as Wheat Pale Green 1 (WPG1), which was further mapped to a physical interval of 34.69 M-41.19 M on chromosome 2A. Transcriptomic analysis revealed that expression of photosynthesis-related genes, and N absorption and transportation genes consistently decreased in wpg1, which revalidated the underlying relationship between N shortage and leaf chlorisis. The results presented here lays the basis for further dissecting the causal gene of WPG1 and the subsequent molecular mechanism underlying the regulation of leaf senescence, N allocation, and possibly the photosynthesis in wheat.
Indexed as
Identifiers
41343053What OpenQuestion holds
Registered trials
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 OpenQuestion graph.