Wang Ying, Wang Lingping, Xing Nailin, Wu Xiaohua, Wu Xinyi, Wang Baogen, Lu Zhongfu, Xu Pei, Tao Ye, Li Guojing, Wang Yuhong
1Institute of Vegetables, Zhejiang Academy of Agricultural Sciences, Hangzhou, 310021 China.
2Institute of Vegetables, Ningbo Academy of Agricultural Sciences, Ningbo, 315040 China.
Hortic Res. 2020 Feb 1;7:13. doi: 10.1038/s41438-019-0236-1. eCollection 2020.
Heterografting has long been used to enhance the chilling tolerance of temperature-sensitive crops, including watermelon, whose mechanism is known to involve bidirectional long-distance mRNA movements. Despite several studies reporting on mobile mRNA (mb-mRNA) profiles in plants, accurate identification of mb-mRNAs is challenging owing to an array of technical problems. Here, we developed a bioinformatical pipeline that took most of the known technical concerns into consideration and is considered to be a universal tool for mb-mRNA detection in heterografts. By applying this pipeline to a commercial watermelon-bottle gourd heterografting system, we detected 130 and 1144 mb-mRNAs upwardly and 167 and 1051 mb-mRNAs downwardly transmitted under normal and chilling-stress conditions, respectively. Quantitative real-time PCR indicated a high accuracy rate (88.2%) of mb-mRNA prediction with our pipeline. We further revealed that the mobility of mRNAs was not associated with their abundance. Functional annotation and classification implied that scions may convey the stress signal to the rootstock, subsequently triggering energy metabolism reprogramming and abscisic acid-mediated stress responses by upward movement of effective mRNAs, ultimately leading to enhanced chilling tolerance. This study provides a universal tool for mb-mRNA detection in plant heterografting systems and novel insights into heterografting advantages under chilling stress.
异种嫁接长期以来一直被用于提高包括西瓜在内的温度敏感型作物的耐寒性,其机制已知涉及双向长距离mRNA移动。尽管有几项研究报告了植物中移动mRNA(mb-mRNA)的概况,但由于一系列技术问题,准确鉴定mb-mRNA具有挑战性。在这里,我们开发了一种生物信息学流程,该流程考虑了大多数已知的技术问题,被认为是异种嫁接中mb-mRNA检测的通用工具。通过将此流程应用于商业西瓜-葫芦异种嫁接系统,我们分别在正常和冷胁迫条件下检测到向上传输的130个和1144个mb-mRNA以及向下传输的167个和1051个mb-mRNA。定量实时PCR表明我们的流程对mb-mRNA的预测准确率很高(88.2%)。我们进一步揭示,mRNA的移动性与其丰度无关。功能注释和分类表明,接穗可能将胁迫信号传递给砧木,随后通过有效mRNA的向上移动触发能量代谢重编程和脱落酸介导的胁迫反应,最终导致耐寒性增强。本研究为植物异种嫁接系统中mb-mRNA的检测提供了一种通用工具,并对冷胁迫下异种嫁接的优势提供了新的见解。