Manipulation of DET1 expression in tomato results in photomorphogenic phenotypes caused by post-transcriptional gene silencing
The tomato HIGH PIGMENT-2 gene encodes an orthologue of the Arabidopsis nuclear protein DE-ETIOLATED 1 (DET1). From genetic analyses it has been proposed that DET1 is a negative regulator of light signal transduction, and recent results indicate that it may control light-regulated gene expression at...
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Published in | The Plant journal : for cell and molecular biology Vol. 40; no. 3; pp. 344 - 354 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Science Ltd
01.11.2004
Blackwell Science Blackwell Publishing Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | The tomato HIGH PIGMENT-2 gene encodes an orthologue of the Arabidopsis nuclear protein DE-ETIOLATED 1 (DET1). From genetic analyses it has been proposed that DET1 is a negative regulator of light signal transduction, and recent results indicate that it may control light-regulated gene expression at the level of chromatin remodelling. To gain further understanding about the function of DET1 during plant development, we generated a range of overexpression constructs and introduced them into tomato. Unexpectedly, we only observed phenotypes characteristic of DET1 inactivation, i.e. hyper-responsiveness to light. Molecular analysis indicated in all cases that these phenotypes were a result of suppression of endogenous DET1 expression, due to post-transcriptional gene silencing. DET1 silencing was often lethal when it occurred at relatively early stages of plant development, whereas light hyper-responsive phenotypes were obtained when silencing occurred later on. The appearance of phenotypes correlated with the generation of siRNAs but not DNA hypermethylation, and was most efficient when using constructs with mutations in the DET1 coding sequence or with constructs containing only the 3'-terminal portion of the gene. These results indicate an important function for DET1 throughout plant development and demonstrate that silencing of DET1 in fruits results in increased carotenoids, which may have biotechnological potential. |
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Bibliography: | † ‡ Present address: Verdia Inc., 200 Penobscot Drive, Redwood City, CA 94063, USA. Present address: Department of Horticultural Sciences, Vegetable & Fruit Improvement Center, Texas A & M University, College Station, TX 77843‐2119, USA. Present address: Crop and Food Research, Food Industry Science Centre, Batchelar Road, Palmerston North, New Zealand. ¶ § Present address: Laboratory for Plant Physiology, Wageningen University, Arboretumlaan 4, 6703 BD Wageningen, The Netherlands. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 Present address: Department of Horticultural Sciences, Vegetable & Fruit Improvement Center, Texas A & M University, College Station, TX 77843-2119, USA. |
ISSN: | 0960-7412 1365-313X |
DOI: | 10.1111/j.1365-313x.2004.02218.x |