品种与技术

籼稻恢复系R382苗期耐冷生理机制与基因表达特性分析

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  • 1 湖南农业大学 农学院, 长沙 410128
    2 湖南杂交水稻研究中心, 长沙 410125
第一联系人:

第一作者:13364950541@163.com

收稿日期: 2026-03-12

  网络出版日期: 2026-07-14

基金资助

岳麓山实验室种业专项-重大新品种培育项目(YLS-2025-ZY02001);岳麓山实验室种业专项-青年项目(YLS-2025-ZY04023);湖南省科技创新计划项目(2024RC3183);长沙市自然科学基金(kq2502269)

Analysis of Chilling Tolerance Physiological Mechanism and Gene Expression Characteristics of Indica Rice Restorer Line R382 at the Seedling Stage

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  • 1 College of Agronomy, Hunan Agricultural University, Changsha 410128, China
    2 Hunan Hybrid Rice Research Center, Changsha 410125, China
First author contact:

1st author: 13364950541@163.com

Received date: 2026-03-12

  Online published: 2026-07-14

摘要

本研究对26个杂交籼稻恢复系进行苗期耐冷性评价,鉴定出强耐冷性恢复系R382;以大面积推广应用但耐冷性较弱的恢复系9311为对照,通过比较R382与9311耐冷相关生理指标及低温应答基因表达水平的差异,揭示了R382苗期耐冷的生理机制。在相同生长环境下,系统分析了常温及低温胁迫条件下,R382和9311水稻幼苗叶片的多项生理指标变化,包括活性氧(过氧化氢、超氧阴离子)水平、丙二醛含量、抗氧化酶活性、相对电导率及渗透保护物质脯氨酸含量等。同时,采用实时定量PCR技术,检测了苗期低温胁迫下抗氧化酶编码基因(过氧化氢酶OsCATB、超氧化物歧化酶OsFe-SOD、抗坏血酸过氧化物酶OsAPX1)及富含脯氨酸蛋白编码基因OsPRP1的表达水平。结果表明,低温胁迫后,R382的抗氧化酶编码基因表达水平显著高于9311,抗氧化酶活性更强,活性氧及毒性化合物丙二醛积累量更少;同时,其细胞内渗透保护物质脯氨酸含量显著升高,细胞相对电导率较低,这一系列生理及分子层面的差异共同赋予了R382更强的苗期耐冷性。

本文引用格式

张静, 朱童童, 徐佳琛, 李连州, 王昱, 张桂莲, 邓化冰, 卢学丹, 唐文帮 . 籼稻恢复系R382苗期耐冷生理机制与基因表达特性分析[J]. 中国稻米, 2026 , 32(4) : 102 -107 . DOI: 10.3969/j.issn.1006-8082.2026.04.017

Abstract

In this study, 26 indica hybrid rice restorer lines were evaluated for cold tolerance at the seedling stage, and the strongly cold-tolerant restorer line R382 was identified. Using the widely cultivated but relatively cold-sensitive restorer line 9311 as a control, the physiological mechanisms underlying the cold tolerance of R382 at the seedling stage were revealed by comparing differences in cold-related physiological indices and low-temperature-responsive gene expression levels between R382 and 9311. Under identical growth conditions, changes in several physiological parameters of rice seedlings (leaves) of R382 and 9311 were systematically analyzed under both normal temperature and low-temperature stress, including levels of reactive oxygen species (hydrogen peroxide, superoxide anion), malondialdehyde (MDA) content, antioxidant enzyme activities, relative electrolyte leakage, and the osmoprotectant proline content. In addition, real-time quantitative PCR (qRT-PCR) was used to measure the expression levels of genes encoding antioxidant enzymes catalase (OsCATB), iron-superoxide dismutase (OsFe-SOD), ascorbate peroxidase (OsAPX1) and the proline-rich protein gene OsPRP1 under low-temperature stress at the seedling stage. The results showed that after low-temperature treatment, the expression levels of antioxidant enzyme-coding genes in R382 were significantly higher than those in 9311, accompanied by stronger antioxidant enzyme activities, lower accumulation of reactive oxygen species and the toxic compound MDA, and a marked increase in intracellular proline content, along with lower relative electrolyte leakage. These combined physiological and molecular differences contribute to the stronger cold tolerance of R382 at the seedling stage.

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