516 / 2019-03-01 14:48:21
Arabidopsis VAC14 Is Critical for Pollen Development through Mediating Vacuolar Organization
pollen tube,PI(3,5)P2,vacuolar organiztion,VAC14
摘要录用
Li En / Shandong Agricultrual University
Wei-Tong Zhang / Shandong Agricultural University
Yan-Kui Guo / Shandong Agricultural University
Shi-Xia Yu / Shandong Agricultural University
Zhi-Yuan Wan / Shandong Agricultural University
Ting Ma / Shandong Agricultural University
Sha Li / Shandong Agricultural University
Tomoko Hirano / Kyoto Prefectural University
Masa H. Sato / Kyoto Prefectural University
Yan Zhang / Shandong Agricultural University
Pollen viability depends on dynamic vacuolar changes during pollen development. Mutations in FAB1A to FAB1D, the genes encoding phosphatidylinositol 3,5-bisphosphate [PI(3,5)P2]-converting kinases, are male gametophyte lethal in Arabidopsis due to defective vacuolar fission after pollen mitosis I, suggesting a key role of the phospholipid in dynamic vacuolar organization. However, other genetic components that regulate the production of PI(3,5)P2 and its involvement in pollen germination and tube growth are unknown. Here, we identified and characterized Arabidopsis VAC14, a homolog of the yeast and metazoan VAC14s that are crucial for the production of PI(3,5)P2. VAC14 is highly present in developing pollen. Loss of function of VAC14 was male gametophyte lethal due to defective pollen development. Ultrastructural studies showed that vacuolar fission after pollen mitosis I was compromised in vac14 mutant microspores, which led to pollen abortion. We further showed that inhibiting the production of PI(3,5)P2 or exogenous application of PI(3,5)P2 mimicked or rescued the pollen developmental defect of the vac14 mutant, respectively. Genetic interference and pharmacological approaches suggested a role of PI(3,5)P2 in pollen germination and tube growth. Our results provide insights into the function of VAC14 and, by inference, that of PI(3,5)P2 in plant cells.
重要日期
  • 会议日期

    06月16日

    2019

    06月21日

    2019

  • 05月01日 2019

    初稿截稿日期

  • 06月21日 2019

    注册截止日期

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