CLE (CLV3/ESR) is one of the most important groups of peptide phytohormones: its members regulate the development of various plant organs and tissues, as well as interaction with some parasites and symbionts and response to environmental factors. In this regard, the identification and study of the CLE genes encoding the peptides of this group in cultivated plants are of great practical interest. Relatively little is known about the functions of CLE peptides in potato, since the CLE genes of the potato Solanum phureja Juz. et Buk. were characterized only in 2021. At the same time, potato includes plenty of tuberous species of the genus Solanum L., both wild and cultivated, and the diversity of its forms may depend on differences in the sequences of CLE genes. In this work, we performed a search for and analysis of the CLE gene sequences in three wild potato species (S. bukasovii Juz., S. verrucosum Schltdl., S. commersonii Dunal) and four cultivated species (S. chaucha Juz. et Buk., S. curtilobum Juz. et Buk., S. juzepczukii Juz. et Buk., S. ajanhuiri Juz. et Buk.). In total, we identified 332 CLE genes in the analyzed potato species: from 40 to 43 genes of this family for each potato species. All potato species taken for analysis had homologues of previously identified S. phureja CLE genes; at the same time, the CLE42 gene, which is absent from the S. phureja genome, is present in all other analyzed potato species. Polymorphism of CLE proteins of S. commersonii is significantly higher than that of other analyzed potato species, due to the fact that S. commersonii grows in places outside the growing areas of other potato species and this potato is probably not one of the ancestors of cultivated potato. We also found examples of polymorphism of domains of CLE proteins that carried different functions. Further study of potato CLE proteins will reveal their role in development, including regulation of productivity in this important agricultural crop.

In potato, phloem tissues transport sugars and signal molecules to the tuber for growth and storage. The CLAVATA3/ESR-like (CLE) family of plant peptides plays an important role in regulating plant development. In this study, we identified a set of phloem-expressed CLE genes in Solanum tuberosum L. (StCLEs). We analyzed the phloem transcriptome of potato and found that 10 out of 41 StCLE genes were expressed in phloem cells, with StCLE12 and StCLE19 showing the highest expression levels. StCLE12 has an identical CLE domain to the Arabidopsis TDIF peptides, which are known to play a crucial role in maintaining the vascular meristem. StCLE19 has the highest sequence similarity to the Arabidopsis CLE25 peptide, which is involved in the formation of the phloem element and signaling in response to dehydration stress. The overexpression of StCLE12 and another potato TDIF-like gene, StCLE8, promoted vascular cell proliferation and delayed leaf senescence. On the other hand, plants with overexpression of StCLE19 were unable to form adventitious roots and demonstrated the absence of ordered cambium cell layers in the vascular bundles.

Sunflower (Helianthus annuus L.) is specifically infected by an obligatory root parasitic plant Orobanche cumana Wallr. (sunflower broomrape), which causes significant losses of sunflower yield. Breeding of sunflower varieties resistant to broomrape is an important challenge for agriculture. However, the selection of new resistant sunflower varieties was accompanied by the emergence of new virulent races of broomrape, which overcame the effect of resistance genes. Unraveling the molecular mechanisms underlying the resistance to broomrape in sunflowers should facilitate the development of new sunflower varieties with complex resistance to broomrape using genome editing technology. Here, we used CRISPR/Cas9-mediated genome editing in sunflower hairy roots for a specific knock-out of the gene encoding a GRAS transcription factor (HaNSP1a), acting as a possible regulator of strigolactone biosynthesis, a class of phytohormones known to induce the germination of broomrape seeds. According to HPLC-IT-TOF/MS analysis, the levels of orobanchol were decreased in the genetically modified roots with knock-out of the HaNSP1a gene, whereas, in contrast, 5-deoxystrigol levels were increased in the roots with HaNSP1a knock-out, suggesting the role of HaNSP1a in the regulation of the strigolactone biosynthetic pathway. The experimental approach described here could be used in further studies to test the effect of gene knock-out on the development of resistance to O. cumana in sunflowers.

Here, we report the genome sequence of the epiphytic Paenibacillus kyungheensis bacterium isolated from Chenopodium album L. leaves. The raw sequencing data were obtained using the NextSeq 1000 technology (Illumina). The assembly comprises two scaffolds, totaling 5,257,300 bp with a guanine-cytosine content of 39%.

Here, we report the genome sequence of the epiphytic Bacillus safensis Cap07D, a bacterium isolated from Chenopodium album L. seeds. The raw sequencing data were obtained using the NextSeq 1000 technology (Illumina).