Journal Article

<i>Arabidopsis</i> Mutants by Activation Tagging in which Photosynthesis Genes are Expressed in Dedifferentiated Calli

Yasuo Niwa, Shingo Goto, Tatsuo Nakano, Mao Sakaiya, Takanori Hirano, Hirokazu Tsukaya, Yoshibumi Komeda and Hirokazu Kobayashi

in Plant and Cell Physiology

Published on behalf of Japanese Society of Plant Physiologists

Volume 47, issue 3, pages 319-331
Published in print March 2006 | ISSN: 0032-0781
Published online March 2006 | e-ISSN: 1471-9053 | DOI:
Arabidopsis Mutants by Activation Tagging in which Photosynthesis Genes are Expressed in Dedifferentiated Calli

More Like This

Show all results sharing these subjects:

  • Biochemistry
  • Molecular and Cell Biology
  • Plant Sciences and Forestry


Show Summary Details


In an effort to delineate the precise mechanisms underlying the organ-specific expression of photosynthesis genes, Arabidopsis lines homozygous for each transgene construct made with the gene for hygromycin B phosphotransferase or β-glucuronidase (GUS) placed under control of the promoter of the nuclear gene for the small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase (RBCS-3B) were constructed. Furthermore, activation tagging with T-DNA possessing quadruply repeated enhancers derived from the cauliflower mosaic virus 35S promoter was applied to a transgenic line of Arabidopsis. Mutants resistant to hygromycin B during the growth of calli generated from non-green roots on callus-inducing medium resulted from the expression of hygromycin B phosphotransferase driven by the RBCS-3B promoter. Three mutant lines, ces101 to ces103 (callus expression of RBCS), were obtained from approximately 4,000 calli resistant to a selectable marker for transformation. The active transcription driven by the RBCS-3B promoter in all the calli of ces mutants was confirmed by expression of both the GUS reporter gene and endogenous RBCS-3B. Chlorophyll and carotenoids, as well as light-dependent O2 evolution, have been detected in the calli of all ces mutants. The loci where T-DNA was integrated in the ces101 line were determined by thermal asymmetric interlaced (TAIL)-PCR. The introduction of a DNA fragment harboring the gene for receptor-like kinase placed under the influence of enhancers into the parental line reproduced the phenotype of ces mutants. We have thus concluded that CES101 is a receptor-like kinase. The strategy presented in this investigation may promise to select a greater number of ces mutants.

Keywords: Activation tagging; Arabidopsis; Callus; Expression; Mutants; Photosynthesis genes; CAB, chlorophyll a/b-binding proteins; CaMV, cauliflower mosaic virus; ces, callus expression of RBCS; CIM, callus-inducing medium; GUS, β-glucuronidase; MUG, 4-methylumbelliferylglucuronide; RBCS, small subunit of Rubisco; RLK, receptor-like kinase; RT–PCR, reverse transcription–PCR; Rubisco, ribulose 1,5-bisphosphate carboxylase/oxygenase; TAIL-PCR, thermal asymmetric interlaced PCR; uidA, gene for GUS

Journal Article.  7029 words.  Illustrated.

Subjects: Biochemistry ; Molecular and Cell Biology ; Plant Sciences and Forestry

Full text: subscription required

How to subscribe Recommend to my Librarian

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.