論文

査読有り
2008年6月

Targeted degradation of the cyclin-dependent kinase inhibitor ICK4/KRP6 by RING-type E3 ligases is essential for mitotic cell cycle progression during Arabidopsis gametogenesis

PLANT CELL
  • Jingjing Liu
  • Yiyue Zhang
  • Genji Qin
  • Tomohiko Tsuge
  • Norihiro Sakaguchi
  • Guo Luo
  • Kangtai Sun
  • Dongqiao Shi
  • Shiori Aki
  • Nuoyan Zheng
  • Takashi Aoyama
  • Atsuhiro Oka
  • Weicai Yang
  • Masaaki Umeda
  • Qi Xie
  • Hongya Gu
  • Li-Jia Qu
  • 全て表示

20
6
開始ページ
1538
終了ページ
1554
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1105/tpc.108.059741
出版者・発行元
AMER SOC PLANT BIOLOGISTS

Following meiosis, plant gametophytes develop through two or three rounds of mitosis. Although the ontogeny of gametophyte development has been defined in Arabidopsis thaliana, the molecular mechanisms regulating mitotic cell cycle progression are not well understood. Here, we report that RING-H2 group F 1a (RHF1a) and RHF2a, two RING-finger E3 ligases, play an important role in Arabidopsis gametogenesis. The rhf1a rhf2a double mutants are defective in the formation of male and female gametophytes due to interphase arrest of the mitotic cell cycle at the microspore stage of pollen development and at female gametophyte stage 1 of embryo sac development. We demonstrate that RHF1a directly interacts with and targets a cyclin-dependent kinase inhibitor ICK4/KRP6 (for Interactors of Cdc2 Kinase 4/Kip-related protein 6) for proteasome-mediated degradation. Inactivation of the two redundant RHF genes leads to the accumulation of ICK4/KRP6, and reduction of ICK4/KRP6 expression largely rescues the gametophytic defects in rhf1a rhf2a double mutants, indicating that ICK4/KRP6 is a substrate of the RHF E3 ligases. Interestingly, in situ hybridization showed that ICK4/KRP6 was predominantly expressed in sporophytes during meiosis. Our findings indicate that RHF1a/2a-mediated degradation of the meiosis-accumulated ICK4/KRP6 is essential to ensure the progression of subsequent mitoses to form gametophytes in Arabidopsis.

リンク情報
DOI
https://doi.org/10.1105/tpc.108.059741
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/18552199
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000258061200009&DestApp=WOS_CPL
ID情報
  • DOI : 10.1105/tpc.108.059741
  • ISSN : 1040-4651
  • PubMed ID : 18552199
  • Web of Science ID : WOS:000258061200009

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