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  4. 生物時鐘調控甘藷葉部澱粉合成酵素基因表現之分子機制
 
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生物時鐘調控甘藷葉部澱粉合成酵素基因表現之分子機制

Date Issued
2004-07-31
Date
2004-07-31
Author(s)
王淑珍
DOI
922313B002100
URI
http://ntur.lib.ntu.edu.tw//handle/246246/19845
Abstract
A starch granule-bound starch synthase I (GBSSI) gene is regulated by a circadian clock in sweet potato leaves. In order to examine whether the promoter region is responsible for controlling a circadian expression of the GBSSI gene, the sweet potato GBSSI promoter was isolated and deleted to different lengths for functional analysis with a GUS reporter gene in transgenic Arabidopsis plants. Nuclear run-on transcriptional assays showed that the circadian control was regulated at the transcriptional rate level, and de novo synthesized proteins were necessary for controlling the rhythm. Promoter assays showed that the GBSSI promoter fragments containing six I-boxes, two putative circadian regulation elements (CAANNNNATC) and four circadian clock-associated 1 protein-binding sites (AATCT) maintained the activity to induce the circadian expression of the GUS gene. Similar to the GBSSI in sweet potato, GBSSI, soluble starch synthase and ADP-glucose pyrophosphorylase genes in Arabidopsis leaves also exhibited a circadian rhythm. These results suggested that common signals may exist in dicotyledonous plants to coordinate the circadian expression of genes involved in the transitory starch synthetic pathway.
Subjects
Circadian clock
Granule-bound starch synthase
Ipomoea batatas
Starch
Publisher
臺北市:國立臺灣大學農藝學系暨研究所
Type
report
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922313B002100.pdf

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