論文

査読有り 国際共著
2019年8月

High potassium seawater inhibits ascidian sperm chemotaxis, but does not affect the male gamete chemotaxis of a brown alga

Zygote (Cambridge, England)
  • Kinoshita-Terauchi, Nana
  • ,
  • Shiba, Kogiku
  • ,
  • Terauchi, Makoto
  • ,
  • Romero, Francisco
  • ,
  • Ramírez-Gómez
  • ,
  • Héctor Vincente
  • ,
  • Yoshida, Manabu
  • ,
  • Motomura, Taizo
  • ,
  • Kawai, Hiroshi
  • ,
  • Nishigaki, Takuya

27
4
開始ページ
225
終了ページ
231
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1017/S0967199419000224
出版者・発行元
CAMBRIDGE UNIV PRESS

Male gamete chemotaxis towards the female gamete is a general strategy to facilitate the sexual reproduction in many marine eukaryotes. Biochemical studies of chemoattractants for male gametes of brown algae have advanced in the 1970s and 1980s, but the molecular mechanism of male gamete responses to the attractants remains elusive. In sea urchin, a K+ channel called the tetraKCNG channel plays a fundamental role in sperm chemotaxis and inhibition of K+ efflux through this channel by high K+ seawater blocks almost all cell responses to the chemoattractant. This signalling mechanism could be conserved in marine invertebrates as tetraKCNG channels are conserved in the marine invertebrates that exhibit sperm chemotaxis. We confirmed that high K+ seawater also inhibited sperm chemotaxis in ascidian, Ciona intestinalis (robusta), in this study. Conversely, the male gamete chemotaxis towards the female gamete of a brown alga, Mutimo cylindricus, was preserved even in high K+ seawater. This result indicates that none of the K+ channels is essential for male gamete chemotaxis in the brown alga, suggesting that the signalling mechanism for chemotaxis in this brown alga is quite different from that of marine invertebrates. Correlated to this result, we revealed that the channels previously proposed as homologues of tetraKCNG in brown algae have a distinct domain composition from that of the tetraKCNG. Namely, one of them possesses two repeats of the six transmembrane segments (diKCNG) instead of four. The structural analysis suggests that diKCNG is a cyclic nucleotide-modulated and/or voltage-gated K+ channel.

リンク情報
DOI
https://doi.org/10.1017/S0967199419000224
ID情報
  • DOI : 10.1017/S0967199419000224
  • ISSN : 1469-8730

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