Plants are vulnerable to many abiotic stresses, resulting in reduced plant productivity. Its adaptation to unfavorable environments relies on transmitting external stress signals into internal signaling pathways. A series of stress response mechanisms have been developed. Among them, brassinosteroids (BRs) are a class of steroid hormones that are widely involved in plant growth, development, and stress response. Via genetics, proteomics, and genomics studies, the major components of signaling and signaling pathways through a series of phosphorylation cascade reactions have been identified in model plants such as Arabidopsis. Numerous studies have shown that BRs play important roles in plant responses to drought, temperature, salt, heavy metals, and other environmental stresses. The application of BRs to improve plant stress resistance has become the focus of research in recent years, especially the regulation of stress via endogenous BRs. Therefore, this paper systematically summarizes the research progress related to endogenous BR levels and provides an overview of BR biosynthesis and the signaling pathway, as well as the function of endogenous BRs in the response to abiotic stresses.

As a highly conserved family of plant-specific proteins, SIMILAR-TO-RCD-ONE (SROs) play an essential role in plant growth, development and response to abiotic stresses. In this study, six StSRO genes were identified by searching the PARP, RST and WWE domains based on the genome-wide data of potato database DM v6.1, and they were named StSRO1–6 according to their locations on chromosomes. StSRO genes were comprehensively analyzed using bioinformatics methods. The results showed that six StSRO genes were irregularly distributed on five chromosomes. Phylogenetic analysis showed that 30 SRO genes of four species were distributed in three groups, while StSRO genes were distributed in groups II and III. The promoter sequence of StSRO genes contained many cis-acting elements related to hormones and stress responses. In addition, the expression level of StSRO genes in different tissues of doubled monoploid (DM) potato, as well as under salt, drought stresses and hormone treatments, was analyzed by RNA-seq data from the online database and quantitative real-time polymerase chain reaction (qRT-PCR) analysis. Furthermore, the expression level of StSRO genes was analyzed by transcriptome analysis under mild, moderate and severe salt stress. It was concluded that StSRO genes could respond to different abiotic conditions, but their expression level was significantly different. This study lays a foundation for further studies on the biological functions of the StSRO gene family.

TCP is a plant-specific transcription factor that plays an important role in plant growth and development. In this study, we used bioinformatics to identify the entire genome of the TCP gene family in Glycyrrhiza inflata Bat, and we analyzed the expression characteristics of GiTCP genes under UV-B radiation using qRT-PCR. The results were as follows: (1) 24 members of the TCP gene family were identified in G. inflata, evenly distributed on its 24 chromosomes. (2) The GiTCP genes contained 0–4 introns and 0–5 exons. (3) The GiTCP genes were phylogenetically divided into three subfamilies—PCF, CIN, and CYC/TB1, with 14, 9, and 1 GiTCP proteins, respectively. (4) A covariance analysis showed that two pairs of GiTCP genes underwent a fragmentary duplication event. (5) A cis-element analysis showed that the cis-responsive elements of the GiTCP genes’ promoter regions were mainly comprised of light-responsive, stress-responsive, hormone-regulated, growth and development, and metabolic-regulated elements. (6) A protein network interaction analysis revealed a total of 14 functional molecules of TCPs and 8 potential interacting proteins directly related to GiTCP proteins. (7) GO annotation showed that the GiTCP genes were mainly enriched in BP, CC, and MF groups and had corresponding functions. (8) RNA-seq and qRT-PCR further indicated that GiTCP3, 6, 7, 8, 12, 14, 17, 23, and 24 were up- or down-regulated in G. inflata after UV-B radiation, demonstrating that these genes responded to UV-B radiation in G. inflata. (9) Subcellular localization analysis showed that the GiTCP8 protein was localized in the nucleus. The results of this study provide a basis for further exploration of the function of the GiTCP gene family in the growth and development of G. inflata.