生物技术通报 ›› 2026, Vol. 42 ›› Issue (9): 14-28.doi: 10.13560/j.cnki.biotech.bull.1985.2026-0046

• 植物发育生物学专题 • 上一篇    下一篇

温度胁迫调控花药绒毡层发育的研究进展

聂佳1,2, 林慧子1,2, 唐哲源1,2, 陈立余2,3()   

  1. 1.福建农林大学生命科学学院,福州 350002
    2.福建农林大学海峡联合研究院,福州 350002
    3.福建农林大学农学院,福州 350002
  • 收稿日期:2026-01-16 出版日期:2026-09-26 发布日期:2026-09-16
  • 通讯作者: 陈立余lychen@fafu.edu
  • 基金资助:
    国家自然科学基金项目(32170324)

Advances in Regulation of Anther Tapetum Development under Temperature Stress

NIE Jia1,2, LIN Hui-zi1,2, TANG Zhe-yuan1,2, CHEN Li-yu2,3()   

  1. 1.College of Life Sciences, Fujian Agriculture and Forestry University, Fuzhou 350002
    2.Haixia Institute of Science and Technology, Fujian Agriculture and Forestry University, Fuzhou 350002
    3.College of Agriculture, Fujian Agriculture and Forestry University, Fuzhou 350002
  • Received:2026-01-16 Published:2026-09-26 Online:2026-09-16

摘要:

近年来,随着全球气候变暖的加剧,极端天气频发,温度胁迫显著影响花粉育性,给农业生产带来巨大损失。绒毡层是位于花药壁内层的分泌细胞,不仅为小孢子发育提供必需的营养物质,还为花粉外壁的形成提供原料。在花药发育过程中,绒毡层细胞会经历程序性细胞死亡(programmed cell death, PCD),这一过程的提前或延迟均会导致花粉败育。现有研究表明,高温通常会导致绒毡层PCD的提前,而低温则可能抑制或延迟其发生。在此过程中往往伴随着活性氧(reactive oxygen species, ROS)的过度积累及激素信号紊乱,同时影响内质网(endoplasmic reticulum, ER)的结构及功能,导致大量错误折叠及未折叠蛋白质积累。温度胁迫还可能直接影响蛋白质的降解以破坏蛋白质稳态。此外,花药绒毡层发育及降解的遗传模块DYT1-TDF1-AMS-MYB80-MS1在响应温度胁迫时也发挥着重要作用。本文综述了绒毡层细胞在高低温胁迫下的表型特征,总结了高低温如何通过调控绒毡层DYT1-TDF1-AMS-MYB80-MS1转录激活级联通路的表达,破坏ROS、内质网和蛋白质稳态,以及引起激素信号紊乱来干扰绒毡层发育及PCD时序,进而影响花粉育性。此外,本文还讨论了在有性生殖阶段研究温度胁迫对花粉育性影响的挑战,并展望相关研究在作物育种和农业生产中的潜在应用价值,包括培育耐高低温品种、丰富作物抗逆基因库、优化栽培管理策略、研发新型化学药剂等方面。

关键词: 温度胁迫, 绒毡层, 程序性细胞死亡, 花粉育性, 活性氧, 激素信号, 内质网应激, 蛋白质稳态

Abstract:

With the escalation of global warming, extreme weather events have become more frequent, leading to temperature stress that severely compromises pollen fertility and results in significant agricultural losses. The tapetum, consisting of secretory cells located in the inner wall of the anther, provides vital nutrients for microspore development and materials essential for pollen exine formation. During anther development, tapetum cells undergo programmed cell death (PCD); deviations in the timing of this process, whether premature or delayed, can lead to pollen sterility. Recent studies indicate that high temperatures primarily trigger early PCD in tapetum cells, whereas low temperatures tend to inhibit or delay it. This process is often accompanied by excessive accumulation of reactive oxygen species (ROS) and hormone signaling disruption. Additionally, temperature stress induces structural and functional abnormalities in the endoplasmic reticulum (ER), resulting in massive accumulation of misfolded and unfolded proteins. Temperature stress can also directly disrupt protein homeostasis by interfering with protein degradation. Furthermore, the genetic module DYT1-TDF1-AMS-MYB80-MS1, which regulates the development and degradation of the anther tapetum, also plays an important role in responding to temperature stress. In this review, we examine the phenotypic characteristics of tapetal cells under high and low temperature stress, and summarize how these stresses regulate the expression of the tapetal DYT1-TDF1-AMS-MYB80-MS1 transcriptional activation cascade. This regulation disrupts the homeostasis of ROS, ER and proteins, and triggers phytohormone signaling disruption, interfering with tapetal development and the timing of PCD, ultimately affecting pollen fertility. In addition, we discuss the challenges of studying the effects of temperature stress on pollen fertility during the sexual reproductive phase of plants, and explore the potential applications of these studies in crop breeding and agricultural production. These applications include breeding temperature-tolerant cultivars, enriching crop stress resistance gene pools, optimizing cultivation management strategies, and developing novel chemical regulators.

Key words: temperature stress, tapetum, programmed cell death, pollen fertility, reactive oxygen species, hormone signaling, endoplasmic reticulum stress, proteostasis