Abstract

Maximizing the amount of protein translated per unit mRNA is an important goal in establishing expression systems. The 5′ untranslated region (5′-UTR) of mRNA is known to play an important role in determining the rate of translation. The full length 5′-UTR from theArabidopsis thaliana heat shock protein (HSP) gene,HSPI8.2 gene, was inserted into the cloning site between the cauliflower mosaic virus 35S RNA promoter and β-glucuronidase (GUS) gene in the pBI221 plasmid. When this construct was transfected intoNicotiana tabacum (tobacco) BY-2 protoplasts, the level of protein was about 10-fold higher than that of unmodified pB1221. The accumulation of each transcript was the same level. We also demonstrated that the 5′-UTR of theHSP18.2 gene enhances the rate of translation in stable transgenic BY-2 clones andArabidopsis T87 protoplasts. The 5′-UTRs of the otherArabidopsis HSP genes —HSP17.4, HSP81-1,HSP81-2, andHSP81-3 — also conferred efficient translation. These 5′-UTRs ofHSP genes may be of use in increasing the expression of foreign proteins. In combination with a strong promoter, it can be used in the development of efficient protein production systems.

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