Cloning of the promoter sequence of rice OsPR-4b gene and construction of its 5′ deletions for analyzing promoter activity

A 2257 bp promoter sequence upstream of the rice OsPR-4b was amplified using two primers designed on the basis of the sequence of OsPR-4b and rice genome sequences database. Several cis-acting elements, including W-box, PAL-boxA, GT-1 elements and MybSt1 elements, were recognized with the aid of PLA...

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Bibliographic Details
Main Authors: ZHU Ting-heng, LUO Hong-li, SONG Feng-ming, ZHENG Zhong
Format: Article
Language:English
Published: Zhejiang University Press 2005-01-01
Series:浙江大学学报. 农业与生命科学版
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Online Access:https://www.academax.com/doi/10.3785/1008-9209.2005.01.0022
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Summary:A 2257 bp promoter sequence upstream of the rice OsPR-4b was amplified using two primers designed on the basis of the sequence of OsPR-4b and rice genome sequences database. Several cis-acting elements, including W-box, PAL-boxA, GT-1 elements and MybSt1 elements, were recognized with the aid of PLACE program. The promoter region sequence and its 5′ deletion constructs were fused to the gus reportor gene in pCAMBIA1391z vector for analyzing the promoter activity of the cloned promoter sequence and the functions of the cis-acting elements in regulation of OsPR-4b expression.
ISSN:1008-9209
2097-5155