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Tomato SlIDA has a critical role in tomato fertilization by modifying reactive oxygen species homeostasis
Author(s) -
Wang Rong,
Shi ChunLin,
Wang Xiaoyang,
Li Ruizhen,
Meng Yan,
Cheng Lina,
Qi Mingfang,
Xu Tao,
Li Tianlai
Publication year - 2020
Publication title -
the plant journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.058
H-Index - 269
eISSN - 1365-313X
pISSN - 0960-7412
DOI - 10.1111/tpj.14886
Subject(s) - tapetum , biology , reactive oxygen species , pollen tube , microbiology and biotechnology , stamen , programmed cell death , arabidopsis , pollen , abscission , botany , biochemistry , mutant , pollination , apoptosis , gene , microspore
Summary Anther development and pollen tube elongation are key steps for pollination and fertilization. The timing and spatial distribution of reactive oxygen species (ROS) and programmed cell death are central to these processes, but the regulatory mechanism of ROS production is not well understood. Inflorescence deficient in abscission (IDA) is implicated in many plant development and responses to environmental stimuli. However, their role in reproductive development is still unknown. We generated tomato knockout lines ( CR‐slida ) of an IDA homolog ( SlIDA ), which is expressed in the tapetum, septum and pollen tube, and observed a severe defect in male gametes. Further analysis indicated that there was a programmed cell death defect in the tapetum and septum and a failure of anther dehiscence in the CR‐slida lines, likely related to insufficient ROS signal. Liquid chromatography‐tandem mass spectrometry identified mature SlIDA as a 14‐mer EPIP peptide, which was shown to be secreted, and a complementation experiment showed that application of a synthetic 14‐mer EPIP peptide rescued the CR‐slida defect and enhanced the ROS signal. Moreover, the application of the ROS scavengers diphenyleneiodonium or Mn‐TMPP suppressed peptide function. Collectively, our results revealed that SlIDA plays an essential role in pollen development and pollen tube elongation by modulating ROS homeostasis.