Suppr超能文献

转录组分析揭示了棉花根系响应低钾胁迫和钾吸收反馈调节的关键因素。

Transcriptome Analysis Unravels Key Factors Involved in Response to Potassium Deficiency and Feedback Regulation of K Uptake in Cotton Roots.

机构信息

State Key Laboratory of Plant Physiology and Biochemistry, China Agricultural University, Beijing 100193, China.

College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China.

出版信息

Int J Mol Sci. 2021 Mar 19;22(6):3133. doi: 10.3390/ijms22063133.

Abstract

To properly understand cotton responses to potassium (K) deficiency and how its shoot feedback regulates K uptake and root growth, we analyzed the changes in root transcriptome induced by low K (0.03 mM K, lasting three days) in self-grafts of a K inefficient cotton variety (CCRI41/CCRI41, scion/rootstock) and its reciprocal grafts with a K efficient variety (SCRC22/CCRI41). Compared with CCRI41/CCRI41, the SCRC22 scion enhanced the K uptake and root growth of CCRI41 rootstock. A total of 1968 and 2539 differently expressed genes (DEGs) were identified in the roots of CCRI41/CCRI41 and SCRC22/CCRI41 in response to K deficiency, respectively. The overlapped and similarly (both up- or both down-) regulated DEGs in the two grafts were considered the basic response to K deficiency in cotton roots, whereas the DEGs only found in SCRC22/CCRI41 (1954) and those oppositely (one up- and the other down-) regulated in the two grafts might be the key factors involved in the feedback regulation of K uptake and root growth. The expression level of four putative K transporter genes (three and one ) increased in both grafts under low K, which could enable plants to cope with K deficiency. In addition, two ethylene response factors (ERFs), and , both down-regulated in the roots of CCRI41/CCRI41 and SCRC22/CCRI41, may negatively regulate K uptake in cotton roots due to higher net K uptake rate in their virus-induced gene silencing (VIGS) plants. In terms of feedback regulation of K uptake and root growth, several up-regulated DEGs related to Ca binding and CIPK (CBL-interacting protein kinases), one up-regulated and several up-regulated probably play important roles. In conclusion, these results provide a deeper insight into the molecular mechanisms involved in basic response to low K stress in cotton roots and feedback regulation of K uptake, and present several low K tolerance-associated genes that need to be further identified and characterized.

摘要

为了正确理解棉花对钾(K)缺乏的响应以及其地上部反馈如何调节 K 吸收和根系生长,我们分析了低钾(0.03 mM K,持续 3 天)对自嫁接的 K 低效棉花品种(CCRI41/CCRI41,接穗/砧木)和其与 K 高效品种(SCRC22/CCRI41)的互嫁接株根转录组的变化。与 CCRI41/CCRI41 相比,SCRC22 接穗增强了 CCRI41 砧木的 K 吸收和根系生长。在低钾条件下,CCRI41/CCRI41 和 SCRC22/CCRI41 的根系分别鉴定出 1968 和 2539 个差异表达基因(DEGs)。在两个嫁接体中,重叠且相似(均上调或均下调)调节的 DEGs 被认为是棉花根系对 K 缺乏的基本响应,而仅在 SCRC22/CCRI41 中发现的 DEGs(1954 个)和在两个嫁接体中反向(一个上调,另一个下调)调节的 DEGs可能是参与 K 吸收和根系生长反馈调节的关键因素。在低钾条件下,四个假定的 K 转运体基因(三个 和一个 )在两个嫁接体中的表达水平均升高,这可能使植物能够应对 K 缺乏。此外,在 CCRI41/CCRI41 和 SCRC22/CCRI41 的根系中均下调表达的两个乙烯反应因子(ERFs) 和 ,由于其病毒诱导基因沉默(VIGS)植株的净 K 吸收速率较高,可能负调控棉花根系的 K 吸收。就 K 吸收和根系生长的反馈调节而言,几个与 Ca 结合和 CIPK(CBL 相互作用蛋白激酶)相关的上调 DEGs、一个上调的 和几个上调的 可能发挥重要作用。总之,这些结果深入了解了棉花根系对低钾胁迫的基本响应和 K 吸收的反馈调节所涉及的分子机制,并提出了几个需要进一步鉴定和表征的低钾耐受相关基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b6/8003395/7650bbcb87d7/ijms-22-03133-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验