4.7 Article

Hydrogen peroxide signalling mediates fertilization and post-fertilization development in the red alga Bostrychia moritziana

期刊

JOURNAL OF EXPERIMENTAL BOTANY
卷 73, 期 3, 页码 727-741

出版社

OXFORD UNIV PRESS
DOI: 10.1093/jxb/erab453

关键词

Ca2+ influx; fertilization; hydrogen peroxide; ROS signal

资金

  1. Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, and Forestry (IPET) through Golden Seed Project - Ministry of Agriculture, Food and Rural Affairs (MAFRA) [213008-05-5-SB810]
  2. Ministry of Oceans and Fisheries (MOF)
  3. Rural Development Administration (RDA)
  4. Korea Forest Services (KFS)
  5. National Research Foundation of Korea (NRF) [2019M3C1B7025093]
  6. National Research Foundation of Korea [2019M3C1B7025093] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Reactive oxygen species (ROS) signaling plays a crucial role in red algal fertilization, with H2O2 acting as a signaling molecule that regulates gene expression and post-fertilization development possibly through Ca2+ channel activation. NADPH oxidase homologues are involved in fertilization process, and pre-treatment or perturbation of plants' redox state can impact post-fertilization development.
Reactive oxygen species (ROS) signalling has a multitude of roles in cellular processes throughout biology. We hypothesized that red algal fertilization may offer an interesting model to study ROS-mediated signalling, as the stages of fertilization are complex and unique. We detected the localization of ROS production microscopically and monitored the expression of three homologues of NADPH oxidase in reproductive cells during fertilization. ROS were instantaneously produced by spermatia (sperm) when they attached to female trichogynes, diffused across the cell membrane in the form of H2O2, and triggered ROS generation in the carpogonium (egg) as well as carpogonial branch cells which are not in direct contact with spermatia. The expression of NADPH oxidase homologues, RESPIRATORY BURST OXIDASE HOMOLOGUES (BmRBOHs), began to be up-regulated in the female plant upon gamete binding, peaking during the fertilization process and descending back to their original level after fertilization. Pre-treatment with diphenylene iodonium or caffeine blocked gene expression as well as H2O2 production. Post-fertilization development was also inhibited when the redox state of the plants was perturbed with H2O2 at any time before or after the fertilization. Our results suggest that H2O2 acts as an auto-propagating signalling molecule, possibly through Ca2+ channel activation, and regulates gene expression in fertilization as well as post-fertilization development in red algae. A calcium-mediated H(2)O(2)signal regulates RBOHgene expression and mediates spermatial mitosis, gamete fusion, as well as zygote development in red algae.

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