School of Life Sciences, and Hubei Key Laboratory of Genetic Regulation and Integrative Biology, Central China Normal University, Wuhan 430079, Hubei, China.
Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409.
Plant Physiol. 2020 Apr;182(4):1991-2005. doi: 10.1104/pp.19.01149. Epub 2020 Feb 5.
Maintaining the structural integrity of the photosynthetic apparatus during dehydration is critical for effective recovery of photosynthetic activity upon rehydration in a variety of desiccation-tolerant plants, but the underlying molecular mechanism is largely unclear. The subaerial cyanobacterium can survive extreme dehydration conditions and quickly recovers its photosynthetic activity upon rehydration. In this study, we found that the expression of the molecular chaperone NfDnaK2 was substantially induced by dehydration, and NfDnaK2 proteins were primarily localized in the thylakoid membrane. NfDnaJ9 was identified to be the cochaperone partner of NfDnaK2, and their encoding genes shared similar transcriptional responses to dehydration. NfDnaJ9 interacted with the NfFtsH2 protease involved in the degradation of damaged D1 protein. Heterologous expression of enhanced PSII repair and drought tolerance in transgenic sp. PCC 7120. Furthermore, the nitrate reduction (NarL)/nitrogen fixation (FixJ) family transcription factors response regulator (NfRre1) and photosynthetic electron transport-dependent regulator (NfPedR) were identified as putative positive regulators capable of binding to the promoter region of and they may mediate dehydration-induced expression of in Our findings provide novel insights into the molecular mechanism of desiccation tolerance in some xerotolerant microorganisms, which could facilitate future synthetic approaches to the creation of extremophiles in microorganisms and plants.
在各种耐旱植物中,脱水过程中保持光合作用装置的结构完整性对于光合作用活性在再水合后有效恢复至关重要,但潜在的分子机制在很大程度上尚不清楚。陆生蓝细菌 可以在极端脱水条件下生存,并在再水合后迅速恢复其光合作用活性。在这项研究中,我们发现分子伴侣 NfDnaK2 的表达被脱水显著诱导,并且 NfDnaK2 蛋白主要定位于类囊体膜中。鉴定出 NfDnaJ9 是 NfDnaK2 的共伴侣伴侣,它们的编码基因对脱水具有相似的转录响应。NfDnaJ9 与参与 D1 蛋白降解的 NfFtsH2 蛋白酶相互作用。异源表达 增强了转基因 sp. PCC 7120 的 PSII 修复和耐旱性。此外,硝酸盐还原 (NarL)/固氮 (FixJ) 家族转录因子响应调节剂 (NfRre1) 和光合电子传递依赖性调节剂 (NfPedR) 被鉴定为可能的正调节因子,能够结合到 和它们可能介导脱水诱导的表达 在我们的研究结果为一些耐旱微生物的脱水耐受性的分子机制提供了新的见解,这可能有助于未来在微生物和植物中创造极端微生物的合成方法。