Cheng Chen, Wang Jianfeng, Hou Wenpeng, Malik Kamran, Zhao Chengzhou, Niu Xueli, Liu Yinglong, Huang Rong, Li Chunjie, Nan Zhibiao
State Key Laboratory of Grassland Agro-Ecosystems, Center for Grassland Microbiome, Lanzhou University, Lanzhou 730000, China.
College of Pastoral Agriculture Science and Technology, Lanzhou University, Lanzhou 730000, China.
Int J Mol Sci. 2021 Dec 7;22(24):13191. doi: 10.3390/ijms222413191.
Seed-borne endophyte enhance NaCl tolerance in and increase its biomass. However, the molecular mechanism by which increases the tolerance of host grasses to NaCl stress is unclear. Hence, we firstly explored the full-length transcriptome information of by PacBio RS II. In this work, we obtained 738,588 full-length non-chimeric reads, 36,105 transcript sequences and 27,202 complete CDSs from . We identified 3558 transcription factors (TFs), 15,945 simple sequence repeats and 963 long non-coding RNAs of . The present results show that 2464 and 1817 genes were differentially expressed by in the leaves of E+ and E- plants at 0 mM and 200 mM NaCl concentrations, respectively. In addition, NaCl stress significantly regulated 4919 DEGs and 502 DEGs in the leaves of E+ and E- plants, respectively. Transcripts associated with photosynthesis, plant hormone signal transduction, amino acids metabolism, flavonoid biosynthetic process and WRKY TFs were differentially expressed by ; importantly, up-regulated biology processes (brassinosteroid biosynthesis, oxidation-reduction, cellular calcium ion homeostasis, carotene biosynthesis, positive regulation of proteasomal ubiquitin-dependent protein catabolism and proanthocyanidin biosynthesis) of host grass under NaCl stress, which indicated an increase in the ability of host grasses' adaptation to NaCl stress. In conclusion, our study demonstrates the molecular mechanism for to increase the tolerance to salt stress in the host, which provides a theoretical basis for the molecular breed to create salt-tolerant forage with endophytes.
种子内生菌提高了[植物名称]对NaCl的耐受性并增加了其生物量。然而,[植物名称]提高宿主草对NaCl胁迫耐受性的分子机制尚不清楚。因此,我们首先通过PacBio RS II探索了[植物名称]的全长转录组信息。在这项工作中,我们从[植物名称]获得了738,588条全长非嵌合reads、36,105个转录序列和27,202个完整的CDS。我们鉴定了[植物名称]的3558个转录因子(TFs)、15,945个简单序列重复和963个长链非编码RNA。目前的结果表明,在0 mM和200 mM NaCl浓度下,E+和E-植株叶片中分别有2464个和1817个基因差异表达。此外,NaCl胁迫分别显著调节了E+和E-植株叶片中的4919个差异表达基因(DEGs)和502个DEGs。与光合作用、植物激素信号转导、氨基酸代谢、类黄酮生物合成过程和WRKY TFs相关的转录本差异表达;重要的是,[植物名称]上调了宿主草在NaCl胁迫下的生物学过程(油菜素类固醇生物合成、氧化还原、细胞钙离子稳态、类胡萝卜素生物合成、蛋白酶体泛素依赖性蛋白分解代谢的正调控和原花青素生物合成),这表明宿主草对NaCl胁迫的适应能力增强。总之,我们的研究揭示了[植物名称]提高宿主对盐胁迫耐受性的分子机制,为通过分子育种培育含内生菌的耐盐饲料提供了理论依据。