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Plant and Cell Physiology, 2003, Vol. 44, No. 5 491-499
© 2003 Oxford University Press

A Mechanism for Light-Induced Translation of the rbcL mRNA Encoding the Large Subunit of Ribulose-1,5-bisphosphate Carboxylase in Barley Chloroplasts

Jungmook Kim1,2 and John E. Mullet

Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, U.S.A.

Translational regulation plays a key role in light-induced expression of photosynthesis-related genes at various levels in chloroplasts. We here present the results suggesting a mechanism for light-induced translation of the rbcL mRNA encoding the large subunit (LS) of ribulose-1,5-bisphosphate carboxylase (Rubisco). When 8-day-old dark-grown barley seedlings that have low plastid translation activity were illuminated for 16 h, a dramatic increase in synthesis of large subunit of Rubisco and global activation of plastid protein synthesis occurred. While an increase in polysome-associated rbcL mRNA was observed upon illumination for 16 h, the abundance of translation initiation complexes bound to rbcL mRNA remained constant, indicating that translation elongation might be controlled during this dark-to-light transition. Toeprinting of soluble rbcL polysomes after in organello plastid translation showed that ribosomes of rbcL translation initiation complexes could read-out into elongating ribosomes in illuminated plastids whereas in dark-grown plastids, read-out of ribosomes of translation initiation complexes was inhibited. Moreover, new rounds of translation initiation could also occur in illuminated plastids, but not in dark-grown plastids. These results suggest that translation initiation complexes for rbcL are normally formed in the dark, but the transition step of translation initiation complexes entering the elongation phase of protein synthesis and/or the elongation step might be inhibited, and this inhibition seems to be released upon illumination. The release of such a translational block upon illumination may contribute to light-activated translation of the rbcL mRNA.

1 Present address: Kumho Life and Environmental Science Laboratory, 1 Oryong-Dong, Puk-Gu, Gwangju, 500-712 Korea.

2 Corresponding author: E-mail, jungmkim{at}kkpc.com; Fax, +82-62-972-5085.


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