The ideal plant architecture is a critical factor in achieving high yields in tomato (Solanum lycopersicum) cultivation.  The length and number of internodes directly influence plant height.  Therefore, investigating the regulatory mechanisms of internode morphology is essential for the genetic enhancement of tomatoes.  We identified a naturally occurring field mutant, tomato elongated internode (tei), characterized by longer internodes and darker leaf color.  Physiological hormone and microscopic studies revealed that, compared to wild-type (WT) plants, the tei mutant exhibited increased endogenous GA3 levels, enhanced photosynthetic capacity, and elongation of stem internode cells.  RNA-seq analysis results of tei and WT indicated enrichment in the gibberellin pathway.  We employed BSA-seq for mapping analysis on tei, WT, and F₂ populations, leading to the fine mapping of the candidate gene designated as TEI (Tomato Elongated Internode).  This gene encoded a gibberellin 20 oxidase (GA20ox) protein and was identified as Solyc09g042210.  Additionally, we discovered numerous SNPs and InDel mutations in the TEI promoter region, with expression levels of TEI in tei stems significantly higher than those in WT.  Furthermore, knocking out the TEI gene eliminated its role in elongating internodes.  We proposed that TEI serves as the primary effector gene regulating the internode elongation phenotype associated with tei.  This discovery offered researchers a novel target for enhancing crop plant varieties by modulating gibberellin homeostasis, ultimately contributing to the breeding of superior tomato varieties.

The evolutionary development of adventitious roots (ARs) in plants enhances their capacity to adapt to various stress conditions. A thorough analysis of the influencing factors in its morphological construction holds significant theoretical value and practical guidance for overcoming rooting obstacles in cuttings, as well as for cultivating superior varieties characterized by broad adaptability and stress resistance. In this study, we investigated the molecular mechanisms underlying the development of ARs in tomato (Solanum lycopersicum).by performing transcriptome sequencing (RNA-seq). We analyzed the transcription profiles of relevant genes in the "Y962" strain, which exhibits spontaneous AR formation, and the "W961" strain, which does not form ARs. Our findings indicate that the AR induction stage represents an active phase of development, during which we identified 1,676 overlapping genes across the three comparison groups, highlighting the most differentially expressed genes. Functional enrichment analysis showed that they were most closely related to response to auxin, and were also dependent on the crosstalk between other hormones and carbohydrates. Furthermore, through the measurement of endogenous auxin levels and the induction tests with exogenous auxin, it was established that the formation of ARs is closely linked to the accumulation and transport of auxin. Notably, the auxin efflux SlPIN3, which was enriched in the auxin response pathway, exhibited significantly high expression during the induction phase of ARs. The slpin3 mutant, generated using the CRISPR/Cas9 editing system, exhibited a significant reduction in the number of ARs, highlighting the close relationship between polar transport regulated by SlPIN3 and auxin-induced AR formation. In summary, this study not only enriches the developmental network of AR formation in tomatoes with a wealth of data but also elucidates the potential mechanisms for promoting AR development by targeting SlPIN3.