MISC

2003年7月

Mechanism regulating telomerase activity in Oryza sativa L.

PLANT SCIENCE
  • H Chung
  • ,
  • Y Hirata
  • ,
  • S Ando
  • ,
  • S Kamachi
  • ,
  • S Sakai

165
1
開始ページ
43
終了ページ
54
記述言語
英語
掲載種別
DOI
10.1016/S0168-9452(03)00124-9
出版者・発行元
ELSEVIER SCI IRELAND LTD

A stretch PCR-based method used to measure human telomerase activity was modified for use with plant telomerase and shown to be useful for quantitative analysis. We isolated a full-length cDNA of a telomerase reverse transcriptase catalytic subunit gene from suspension-cultured cells of rice (Oryza sativa L.). A single copy of this gene is present in the rice genome. Telomerase activity was detected in suspension-cultured O. saliva cells at all growth stages, although the activity was greatest in 2-day-old subcultures and decreased at 6 days. Nevertheless, the accumulation of O. sativa telomerase mRNA was nearly constant in cells at all growth stages. Although no telomerase activity was detected in the lower portions of blades in 3-month-old rice plants, telomerase mRNA accumulated in the blades. Tests of different tissues excised from rice seedlings 3 weeks after sowing showed that root tips had high telomerase activity, while roots without root tips had no telomerase activity. Nevertheless, telomerase mRNA accumulated in both tissues. These results suggest that telomerase activity in tissues of O. saliva is regulated at the post-transcriptional or post-translational levels. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/S0168-9452(03)00124-9
CiNii Articles
http://ci.nii.ac.jp/naid/80016025682
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000183926000005&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/S0168-9452(03)00124-9
  • ISSN : 0168-9452
  • CiNii Articles ID : 80016025682
  • Web of Science ID : WOS:000183926000005

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