Journal Article

Cloning Vectors for Rice

Lee, Dong-Yeon, An, Gynheung, Kim, Sung-Ryul, Moon, Sunok, Yang, Jung-Il

2009

Overview

We developed various binary vectors that can be used for expressing a foreign gene in rice. Vectors pGA3426, pGA3436, and pGA3626 are intended for overexpression of a gene using the maize Ubiquitin promoter, whereas pGA3780 is for rather mild expression of a gene using the rice Actin1 promoter. Vector pGA3777 is for expressing two genes simultaneously. We also developed binary vectors for expressing a fusion protein with a tag. Four vectors (pGA3427, pGA3428, pGA3429, and pGA3438) are for protein tags with sGFP, HA, His, and Myc, respectively. Vector pGA3383 is for analyzing promoter activity using the GUS reporter. In this vector, multiple cloning sites in front of GUS can be utilized for accepting a promoter fragment. We also generated transient expression vectors for studying the subcellular localization of a protein. Vectors pGA3452, pGA3651, and pGA3652 are for GFP fusion; pGA3574 for RFP fusion; pGA3697 for Myc tag; and pGA3698 for HA tag. In addition, we generated pGA3506, pGA3516, pGA3592, and pGA3593 for facilitating the subcloning of full-length cDNA clones into our binary vectors.

• Publisher: Springer-Verlag,Springer Nature B.V,한국식물학회
• Subject: Biomedical and Life Sciences / Cloning / Cloning vectors / Enzymes / Expression vectors / Fusion protein / Gene expression / Genes / Genomes / Life Sciences / Localization / Myc protein / Original Research / Plant Breeding/Biotechnology / Plant Ecology / Plant Genetics and Genomics / Plant Sciences / Plant Systematics/Taxonomy/Biogeography / Proteins / Rice / Ubiquitin / 생물학