ABSTRACT
3′-end processing of nucleus-encoded mRNAs includes the addition of a poly(A) tail that is important for translation initiation. Since the vast majority of chloroplast mRNAs acquire their 3′ termini by processing yet are not polyadenylated, we asked whether 3′ end maturation plays a role in chloroplast translation. A general characteristic of the 3′ untranslated regions of chloroplast mRNAs is an inverted repeat (IR) sequence that can fold into a stem-loop structure. These stem-loops and their flanking sequences serve as RNA 3′-end formation signals. Deletion of the Chlamydomonas chloroplast atpB 3′ IR in strain Δ26 results in reduced accumulation of atpB transcripts and the chloroplast ATPase β-subunit, leading to weakly photosynthetic growth. Of the residualatpB mRNA in Δ26, approximately 1% accumulates as a discrete RNA of wild-type size, while the remainder is heterogeneous in length due to the lack of normal 3′ end maturation. In this work, we have analyzed whether these unprocessed atpBtranscripts are actively translated in vivo. We found that only the minority population of discrete transcripts of wild-type size is associated with polysomes and thus accounts for the ATPase β-subunit which accumulates in Δ26. Analysis of chloroplast rbcLmRNA revealed that transcripts extending beyond the mature 3′ end were not polysome associated. These results suggest that 3′-end processing of chloroplast mRNA is required for or strongly stimulates its translation.
ACKNOWLEDGMENTS
This work was supported by United States-Israel Binational Agricultural Research and Development Fund grant nos. US-2207-92 and US-2746-96 and by United States-Israel Binational Science Foundation grant no. 96-00418. H.L. was supported by an NSF grant to D.B.S.