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ID 58130
フルテキストURL
fulltext.pdf 1.97 MB
著者
Imran, Shahin Institute of Plant Science and Resources, Okayama University
Horie, Tomoaki Division of Applied Biology, Faculty of the Textile Science and Technology, Shinshu University
Katsuhara, Maki Institute of Plant Science and Resources, Okayama University ORCID Kaken ID publons researchmap
抄録
OsHKT1;1 in rice, belongs to the high-affinity K+ Transporter family, has been found to be involved in salt tolerance. OsHKT1;1 in japonica rice (Nipponbare) produces mRNA variants, but their functions remain elusive. In salt tolerant rice, Pokkali, eight OsHKT1;1 variants (V1-V8) were identified in addition to the full-length OsHKT1;1 (FL) cDNA. Absolute quantification by qPCR revealed that accumulation of OsHKT1;1-FL mRNA is minor in contrast to that of OsHKT1;1-V1, -V2, -V4, and -V7 mRNAs, all of which are predominant in shoots, while only V1 and V7 mRNAs are predominant in roots. Two electrode voltage clamp (TEVC) experiments using Xenopus laevis oocytes revealed that oocytes-expressing OsHKT1;1-FL from Pokkali exhibited inward-rectified currents in the presence of 96 mM Na+ as reported previously. Further TEVC analyses indicated that six of eight OsHKT1;1 variants elicited currents in a Na+ or a K+ bath solution. OsHKT1;1-V6 exhibited a similar inward rectification to the FL protein. Contrastingly, however, the rests mediated bidirectional currents in both Na+ and K+ bath solutions. These data suggest possibilities that novel mechanisms regulating the transport activity of OsHKT1;1 might exist, and that OsHKT1;1 variants might also carry out distinct physiological roles either independently or in combination with OsHKT1;1-FL.
キーワード
HKT
rice
salt tolerance
Na+ transport
K+ transport
mRNA variants
発行日
2019-12-21
出版物タイトル
Plants
9巻
1号
出版者
MDPI
開始ページ
16
ISSN
2223-7747
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2019 by the authors.
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.3390/plants9010016
ライセンス
http://creativecommons.org/licenses/by/4.0/
助成機関名
文部科学省