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Tissue-specific enhancement of OsRNS1 with root-preferred expression is required for the increase of crop yield.
Gho, Yun-Shil; Choi, Heebak; Moon, Sunok; Kim, Sung-Ryul; Ha, Sun-Hwa; Jung, Ki-Hong.
Afiliación
  • Gho YS; Graduate School of Green-Bio Science & Crop Biotech Institute, Kyung Hee University, Yongin 17104, Republic of Korea.
  • Choi H; Graduate School of Green-Bio Science & Crop Biotech Institute, Kyung Hee University, Yongin 17104, Republic of Korea.
  • Moon S; Graduate School of Green-Bio Science & Crop Biotech Institute, Kyung Hee University, Yongin 17104, Republic of Korea.
  • Kim SR; Strategic Innovation Platform, International Rice Research Institute, Metro Manila, Philippines.
  • Ha SH; Graduate School of Green-Bio Science & Crop Biotech Institute, Kyung Hee University, Yongin 17104, Republic of Korea.
  • Jung KH; Graduate School of Green-Bio Science & Crop Biotech Institute, Kyung Hee University, Yongin 17104, Republic of Korea. Electronic address: khjung2010@khu.ac.kr.
J Adv Res ; 42: 69-81, 2022 12.
Article en En | MEDLINE | ID: mdl-35609869
INTRODUCTION: Root development is a fundamental process that supports plant survival and crop productivity. One of the essential factors to consider when developing biotechnology crops is the selection of a promoter that can optimize the spatial-temporal expression of introduced genes. However, there are insufficient cases of suitable promoters in crop plants, including rice. OBJECTIVES: This study aimed to verify the usefulness of a new rice root-preferred promoter to optimize the function of a target gene with root-preferred expression in rice. METHODS: osrns1 mutant had defects in root development based on T-DNA insertional mutant screening and CRISPR technology. To optimize the function of OsRNS1, we generated OsRNS1-overexpression plants under two different promoters: a whole-plant expression promoter and a novel root-preferred expression promoter. Root growth, yield-related agronomic traits, RNA-seq, and reactive oxygen species (ROS) accumulation were analyzed for comparison. RESULTS: OsRNS1 was found to be involved in root development through T-DNA insertional mutant analysis and gene editing mutant analysis. To understand the gain of function of OsRNS1, pUbi1::OsRNS1 was generated for the whole-plant expression, and both root growth defects and overall growth defects were found. To overcome this problem, a root-preferential overexpression line using Os1-CysPrxB promoter (Per) was generated and showed an increase in root length, plant height, and grain yield compared to wild-type (WT). RNA-seq analysis revealed that the response to oxidative stress-related genes was significantly up-regulated in both overexpression lines but was more obvious in pPer::OsRNS1. Furthermore, ROS levels in the roots were drastically decreased in pPer::OsRNS1 but were increased in the osrns1 mutants compared to WT. CONCLUSION: The results demonstrated that the use of a root-preferred promoter effectively optimizes the function of OsRNS1 and is a useful strategy for improving root-related agronomic traits as well as ROS regulation.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Oryza / Regulación de la Expresión Génica de las Plantas Idioma: En Revista: J Adv Res Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Oryza / Regulación de la Expresión Génica de las Plantas Idioma: En Revista: J Adv Res Año: 2022 Tipo del documento: Article