Pin-Yu Zhu

Auxin response factors (ARFs) are pivotal transcription factors involved in many aspects of auxin-dependent developmental processes. While functions of ARFs have been extensively studied in Arabidopsis, their distinct role in cucumber remains unclear. In this study, a cucumber auxin response factor homolog, CsARF10a, was cloned and overexpressed in tomato plants. RT-qPCR analysis indicated that the expression abundance of CsARF10a was significantly decreased in cucumber leaves and female flowers, and the expression level of CsARF10a was relatively low in pollinated fruits and hormone-treated fruits compared with that in unpollinated fruits. Moreover, the overexpression of CsARF10a in tomato resulted in multiple phenotypic changes, including a wider leaf blade, delayed fruit ripening, and parthenocarpic fruit set in CsARF10a-OE lines. Taken together, our research shed light on the regulatory importance of CsARF10a in regulating various phenotype alterations and laid a solid foundation for further functional studies.

TIR1-like proteins act as auxin receptors and play essential roles in auxin-mediated plant development processes. The number of auxin receptor family members varies among species. While the functions of auxin receptor genes have been widely studied in Arabidopsis, the distinct functions of cucumber (Cucumis sativus L.) auxin receptors remains poorly understood. To further our understanding of their potential role in cucumber development, two TIR1-like genes were identified and designated CsTIR1 and CsAFB2. In the present study, tomato (Sonanum lycopersicum) was used as a model to investigate the phenotypic and molecular changes associated with the overexpression of CsTIR1 and CsAFB2. Differences in the subcellular localizations of CsTIR1 and CsAFB2 were identified and both genes were actively expressed in leaf, female flower and young fruit tissues of cucumber. Moreover, CsTIR1- and CsAFB2-overexpressing lines exhibited pleotropic phenotypes ranging from leaf abnormalities to seed germination and parthenocarpic fruit compared with the wild-type plants. To further elucidate the regulation of CsTIR1 and CsAFB2, the role of the miR393/TIR1 module in regulating cucumber fruit set were investigated. Activation of miR393-mediated mRNA cleavage of CsTIR1 and CsAFB2 was revealed by qPCR and semi-qPCR, which highlighted the critical role of the miR393/TIR1 module in mediating fruit set development in cucumber. Our results provide new insights into the involvement of CsTIR1 and CsAFB2 in regulating various phenotype alterations, and suggest that post-transcriptional regulation of CsTIR1 and CsAFB2 mediated by miR393 is essential for cucumber fruit set initiation. Collectively, these results further clarify the roles of cucumber TIR1 homologs and miR393 in regulating fruit/seed set development and leaf morphogenesis.