{"title":"Genome-wide study of the R2R3-MYB gene family and analysis of NoMYB90 promoting anthocyanin biosynthesis in watercress (Nasturtium officinale R.Br.)","authors":"Suchong Deng, Qiang Ding, Xilin Hou","doi":"10.1016/j.plantsci.2026.113071","DOIUrl":null,"url":null,"abstract":"<div><div>Watercress (<em>Nasturtium officinale</em> R.Br.) is a kind of aquatic or semi-aquatic vegetable, which is rich in a variety of metabolites beneficial to human body. The R2R3-MYB gene family plays a key role in the biosynthesis of metabolites such as anthocyanins, but has not been characterized in watercress. Here, we identified 118 R2R3-NoMYB genes in the watercress genome and classified them into 35 subgroups. High-light treatment simultaneously enhanced anthocyanin accumulation in both lateral stems and upper main stems and strongly up-regulated the expression of subgroup S6 member <em>NoMYB90</em> as well as the anthocyanin biosynthetic structural genes. Subcellular localization showed that NoMYB90 was located in the nucleus and cell membrane. Transient overexpression of <em>NoMYB90</em> in tobacco leaves promoted anthocyanin accumulation, confirming its role as a positive regulator of anthocyanin biosynthesis. Dual-luciferase assay showed that NoMYB90 transactivates the anthocyanin biosynthetic genes <em>NoCHS</em>, <em>NoF3H</em>, <em>NoDFR</em>, and <em>NoUF3GT</em>. This study presented the first genome-wide analysis of the R2R3-MYB family in watercress and identified <em>NoMYB90</em> as a positive regulator of anthocyanin biosynthesis. The findings provided a reference for further investigations of R2R3-NoMYB genes and established a foundation for the study of anthocyanin biosynthesis in watercress.</div></div>","PeriodicalId":20273,"journal":{"name":"Plant Science","volume":"366 ","pages":"Article 113071"},"PeriodicalIF":4.6000,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Science","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0168945226000993","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/23 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Watercress (Nasturtium officinale R.Br.) is a kind of aquatic or semi-aquatic vegetable, which is rich in a variety of metabolites beneficial to human body. The R2R3-MYB gene family plays a key role in the biosynthesis of metabolites such as anthocyanins, but has not been characterized in watercress. Here, we identified 118 R2R3-NoMYB genes in the watercress genome and classified them into 35 subgroups. High-light treatment simultaneously enhanced anthocyanin accumulation in both lateral stems and upper main stems and strongly up-regulated the expression of subgroup S6 member NoMYB90 as well as the anthocyanin biosynthetic structural genes. Subcellular localization showed that NoMYB90 was located in the nucleus and cell membrane. Transient overexpression of NoMYB90 in tobacco leaves promoted anthocyanin accumulation, confirming its role as a positive regulator of anthocyanin biosynthesis. Dual-luciferase assay showed that NoMYB90 transactivates the anthocyanin biosynthetic genes NoCHS, NoF3H, NoDFR, and NoUF3GT. This study presented the first genome-wide analysis of the R2R3-MYB family in watercress and identified NoMYB90 as a positive regulator of anthocyanin biosynthesis. The findings provided a reference for further investigations of R2R3-NoMYB genes and established a foundation for the study of anthocyanin biosynthesis in watercress.
期刊介绍:
Plant Science will publish in the minimum of time, research manuscripts as well as commissioned reviews and commentaries recommended by its referees in all areas of experimental plant biology with emphasis in the broad areas of genomics, proteomics, biochemistry (including enzymology), physiology, cell biology, development, genetics, functional plant breeding, systems biology and the interaction of plants with the environment.
Manuscripts for full consideration should be written concisely and essentially as a final report. The main criterion for publication is that the manuscript must contain original and significant insights that lead to a better understanding of fundamental plant biology. Papers centering on plant cell culture should be of interest to a wide audience and methods employed result in a substantial improvement over existing established techniques and approaches. Methods papers are welcome only when the technique(s) described is novel or provides a major advancement of established protocols.