論文

査読有り
2018年9月26日

Structural analysis of HTL and D14 proteins reveals the basis for ligand selectivity in Striga

Nature Communications
  • Xu Y
  • Miyakawa T
  • Nosaki S
  • Nakamura A
  • Lyu Y
  • Nakamura H
  • Ohto U
  • Ishida H
  • Shimizu T
  • Asami T
  • Tanokura M
  • 全て表示

9
1
開始ページ
3947
終了ページ
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1038/s41467-018-06452-2
出版者・発行元
NATURE PUBLISHING GROUP

HYPOSENSITIVE TO LIGHT (HTL) and DWARF14 (D14) mediate the perception of karrikin and strigolactone, which stimulates germination of the parasitic weed Striga. However, their role in parasitic seeds is poorly understood, and the basis for their differing responsiveness remains unclear. Here, we show that Striga hermonthica HTL proteins (ShHTLs) in 'conserved' and 'intermediate' clades are able to bind karrikin. The 'divergent' clade is able to hydrolyze strigolactone. Unexpectedly, we find that ShD14 is also capable of hydrolyzing strigolactone. Through comparative analysis of ShHTLs and ShD14 crystal structures, we provide insights into the basis for their selectivity. Moreover, we show that both ShD14 and divergent clade ShHTLs, but not conserved and intermediate clade ShHTLs, can interact with the putative downstream signaling component ShMAX2 in the presence of the synthetic strigolactone, rac-GR24. These findings provide insight into how strigolactone is perceived and how ligand specificity is determined.

リンク情報
DOI
https://doi.org/10.1038/s41467-018-06452-2
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/30258184
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000445607500018&DestApp=WOS_CPL
ID情報
  • DOI : 10.1038/s41467-018-06452-2
  • ISSN : 2041-1723
  • PubMed ID : 30258184
  • Web of Science ID : WOS:000445607500018

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