ArticleRice (New York, N.Y.)2026
Identification and Functional Characterization of Anthocyanidin 3-O-Glucosyltransferases OsA3GT1 and OsA3GT2 in Black Rice.
Article in Rice (New York, N.Y.), 2026. 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
15 authors.
Funding
Abstract
Anthocyanins are key pigments that enhance the nutritional value and aesthetic appeal of black rice (Oryza sativa L.), a variety rich in health-promoting compounds. Despite advances in elucidating the anthocyanin biosynthetic pathway, the specific glucosyltransferase responsible for converting anthocyanidins such as cyanidin and peonidin into their 3-O-glucosides remains unidentified in rice. In this study, we identified two isoenzymes of anthocyanidin 3-O-glucosyltransferase, OsA3GT1 and OsA3GT2, in rice and investigated their roles in anthocyanin biosynthesis. Organ-specific expression profiling, subcellular localization, and CRISPR/Cas9-mediated mutagenesis revealed that OsA3GT1 functions as the primary enzyme for anthocyanin biosynthesis in seeds, whereas OsA3GT2 plays a minor role. Loss-of-function mutants of OsA3GT1 exhibited markedly reduced seed pigmentation and anthocyanin content, especially cyanidin 3-O-glucoside and peonidin 3-O-glucoside. Analysis of double mutants further confirmed the pivotal role of OsA3GT1 in anthocyanin biosynthesis. Both OsA3GT1 and OsA3GT2 catalyzed the glucosylation of anthocyanidins and flavonols, showing the highest specificity for the 3-hydroxyl (3-OH) position, consistent with their roles in anthocyanin biosynthesis. Our findings demonstrate that OsA3GT1 plays a major role in anthocyanin biosynthesis, whereas OsA3GT2 contributes to a lesser extent. Functional analysis of OsA3GT1 and OsA3GT2 in black rice, together with in vitro biochemical characterization of recombinant proteins, enhances our understanding of the genetic and biochemical mechanisms underlying anthocyanin biosynthesis in rice grain, providing valuable insights for breeding anthocyanin-enriched rice cultivars.
Indexed as
Identifiers
What 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.