論文

査読有り 筆頭著者
2015年2月

Pale-Green Phenotype of atl31 atl6 Double Mutant Leaves Is Caused by Disruption of 5-Aminolevulinic Acid Biosynthesis in Arabidopsis thaliana

PLOS ONE
  • Shugo Maekawa
  • ,
  • Atsushi Takabayashi
  • ,
  • Thais Huarancca Reyes
  • ,
  • Hiroko Yamamoto
  • ,
  • Ayumi Tanaka
  • ,
  • Takeo Sato
  • ,
  • Junji Yamaguchi

10
2
開始ページ
e0117662
終了ページ
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1371/journal.pone.0117662
出版者・発行元
PUBLIC LIBRARY SCIENCE

Arabidopsis ubiquitin ligases ATL31 and homologue ATL6 control the carbon/nitrogen nutrient and pathogen responses. A mutant with the loss-of-function of both atl31 and atl6 developed light intensity-dependent pale-green true leaves, whereas the single knockoutmutants did not. Plastid ultrastructure and Blue Native-PAGE analyses revealed that pale-green leaves contain abnormal plastid structure with highly reduced levels of thylakoid proteins. In contrast, the pale-green leaves of the atl31/atl6 mutant showed normal Fv/Fm. In the pale-green leaves of the atl31/atl6, the expression of HEMA1, which encodes the key enzyme for 5-aminolevulinic acid synthesis, the rate-limiting step in chlorophyll biosynthesis, was markedly down-regulated. The expression of key transcription factor GLK1, which directly promotes HEMA1 transcription, was also significantly decreased in atl31/atl6 mutant. Finally, application of 5-aminolevulinic acid to the atl31/atl6 mutants resulted in recovery to a green phenotype. Taken together, these findings indicate that the 5-aminolevulinic acid biosynthesis step was inhibited through the down-regulation of chlorophyll biosynthesis-related genes in the pale-green leaves of atl31/atl6 mutant.

リンク情報
DOI
https://doi.org/10.1371/journal.pone.0117662
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/25706562
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000350662100109&DestApp=WOS_CPL
ID情報
  • DOI : 10.1371/journal.pone.0117662
  • ISSN : 1932-6203
  • PubMed ID : 25706562
  • Web of Science ID : WOS:000350662100109

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