van Overbeek Leonard S, Aanstoot Stefan, Esveld Erik, Russ Lina, Andreo Jimenez Beatriz
Wageningen University and Research (WUR), Radix building (building 107), Droevendaalsesteeg 1, 6700AB Wageningen, The Netherlands.
FEMS Microbiol Ecol. 2025 Jun 24;101(7). doi: 10.1093/femsec/fiaf063.
Roots are essential plant organs for anchorage in soil, uptake of water with nutrients, storage of photosynthates, and microbial interactions. More knowledge on microorganisms stimulating root growth is needed to control root development of cultured plants. A marker-assisted approach would facilitate vast screenings of microbes for eventual effects on root development. It was aimed to select for transcripts that report on root growth stimulation at the early tomato plant growth stage upon microbial treatments. Microbially treated tomato (Solanum lycopersicum) plants were cultivated in stone wool slabs and screened for genes that increased or decreased in differential expression upon increased root growth, by RNAseq. Expression of 21 selected genes was measured by quantitative polymerase chain reaction (qPCR) in relation with stimulated root growth, recorded by X-ray microtomography, of microbially treated tomato plants cultivated in stone wool blocks. Two genes were identified of which expression significantly correlated with high measured root length, and for one also with high measured shoot wet and dry weight. The translated products, both involved in modulation of Rubisco activity, were a chloroplast-localized acetyltransferase (SlSNAT2) and a Rubisco activase (Rca). Transcripts whose translated products modulate Rubisco activity can serve as candidates for reporting on early root development upon microbial inoculation.
根是植物的重要器官,用于在土壤中固定植株、吸收水分和养分、储存光合产物以及进行微生物相互作用。为了控制栽培植物的根系发育,需要更多关于刺激根系生长的微生物的知识。标记辅助方法将有助于对微生物进行大规模筛选,以确定其对根系发育的最终影响。本研究旨在筛选出在番茄植株生长早期经微生物处理后能反映根系生长受刺激情况的转录本。将经微生物处理的番茄(Solanum lycopersicum)植株种植在岩棉板上,并通过RNA测序筛选出在根系生长增加时差异表达上调或下调的基因。通过定量聚合酶链反应(qPCR)测定了21个选定基因的表达,这些基因与在岩棉块中种植的经微生物处理的番茄植株的根系生长受刺激情况相关,根系生长情况通过X射线显微断层扫描记录。鉴定出两个基因,其表达与测量到的高根长显著相关,其中一个基因还与测量到的高地上部分湿重和干重显著相关。这两个基因的翻译产物均参与调节Rubisco活性,分别是一个定位于叶绿体的乙酰转移酶(SlSNAT2)和一个Rubisco活化酶(Rca)。其翻译产物调节Rubisco活性的转录本可作为报告微生物接种后早期根系发育情况的候选基因。