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转录因子 MYC2 样蛋白与 OsCYP2 启动子的 ABRE 结合增强了水稻的耐盐性。

Binding of the transcription factor MYC2-like to the ABRE of the OsCYP2 promoter enhances salt tolerance in Oryza sativa.

机构信息

Key Laboratory for Quality Improvement of Agricultural Products of Zhejiang Province, College of Advanced Agricultural Sciences, Zhejiang A & F University, Hangzhou, China.

出版信息

PLoS One. 2022 Oct 14;17(10):e0276075. doi: 10.1371/journal.pone.0276075. eCollection 2022.

DOI:10.1371/journal.pone.0276075
PMID:36240213
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9565382/
Abstract

Cyclophilins, a type of peptidyl-prolyl cis-trans isomerase, function as important molecular chaperones in a series of biological processes. However, the expression pattern and signal transduction pathway of cyclophilins are still unclear. Here, we showed that the promoter of OsCYP2 could function as a tissue-specific promoter by GUS staining. Moreover, we found that the promoter sequence contained not only core elements but also inducible elements. Then, the ABA-responsive element was used for cDNA library screening, and the transcription factor MYC2-like was identified by a yeast one-hybrid assay and confirmed through an electrophoretic mobility shift assay. Furthermore, the relative expression showed that MYC2-like was induced by abscisic acid. In addition, MYC2-like overexpression enhanced salt tolerance in transformants and partially restored the cyp2-RNAi line. In summary, we explored a novel transcriptional signal mediated by MYC2-like, a potential regulator of salt stress-related physiological processes in rice.

摘要

亲环蛋白属于肽基脯氨酰顺反异构酶,作为重要的分子伴侣在一系列生物学过程中发挥功能。然而,亲环蛋白的表达模式和信号转导途径仍不清楚。在这里,我们通过 GUS 染色显示 OsCYP2 的启动子可以作为组织特异性启动子发挥作用。此外,我们发现启动子序列不仅包含核心元件,还包含诱导元件。然后,我们使用 ABA 响应元件进行 cDNA 文库筛选,并通过酵母单杂交测定鉴定出转录因子 MYC2-like,随后通过电泳迁移率变动测定得到验证。此外,相对表达分析表明 MYC2-like 受到脱落酸的诱导。此外,MYC2-like 的过表达增强了转化体的耐盐性,并部分恢复了 cyp2-RNAi 系。总之,我们探索了由 MYC2-like 介导的一种新的转录信号,它可能是水稻中与盐胁迫相关的生理过程的调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/c673c974081b/pone.0276075.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/71d0a5ddd4ae/pone.0276075.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/3c76148650d5/pone.0276075.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/83eee5ac1415/pone.0276075.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/93e2405a56b2/pone.0276075.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/364844c05f4d/pone.0276075.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/c673c974081b/pone.0276075.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/71d0a5ddd4ae/pone.0276075.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/3c76148650d5/pone.0276075.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/83eee5ac1415/pone.0276075.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/93e2405a56b2/pone.0276075.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/364844c05f4d/pone.0276075.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bbf/9565382/c673c974081b/pone.0276075.g006.jpg

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