TY - JOUR
T1 - The downstream atpE cistron is efficiently translated via its own cis-element in partially overlapping atpB-atpE dicistronic mRNAs in chloroplasts
AU - Suzuki, Haruka
AU - Kuroda, Hiroshi
AU - Yukawa, Yasushi
AU - Sugiura, Masahiro
N1 - Funding Information:
Nagoya City University Funds; New Energy and Industrial Technology Development Organization; Grants-in-Aid for Scientific Research (15370025, 17370020 to M.S., 20570043 to H.K.). Funding for open access charge: Grant-in-Aid for Scientific Research (1737002).
PY - 2011/11
Y1 - 2011/11
N2 - The chloroplast atpB and atpE genes encode subunits β and of the ATP synthase, respectively. They are co-transcribed as dicistronic mRNAs in flowering plants. An unusual feature is an overlap (AUGA) of the atpB stop codon (UGA) with the atpE start codon (AUG). Hence, atpE translation has been believed to depend on atpB translation (i.e. translational coupling). Using an in vitro translation system from tobacco chloroplasts, we showed that both atpB and atpE cistrons are translated from the tobacco dicistronic mRNA, and that the efficiency of atpB translation is higher than that of atpE translation. When the atpB 5′-UTR was replaced with lower efficiency 5′-UTRs, atpE translation was higher than atpB translation. Removal of the entire atpB 5′-UTR arrested atpB translation but atpE translation still proceeded. Introduction of a premature stop codon in the atpB cistron did not abolish atpE translation. These results indicate that atpE translation is independent of atpB translation. Mutation analysis showed that the atpE cistron possesses its own cis-element(s) for translation, located ∼25nt upstream from the start codon.
AB - The chloroplast atpB and atpE genes encode subunits β and of the ATP synthase, respectively. They are co-transcribed as dicistronic mRNAs in flowering plants. An unusual feature is an overlap (AUGA) of the atpB stop codon (UGA) with the atpE start codon (AUG). Hence, atpE translation has been believed to depend on atpB translation (i.e. translational coupling). Using an in vitro translation system from tobacco chloroplasts, we showed that both atpB and atpE cistrons are translated from the tobacco dicistronic mRNA, and that the efficiency of atpB translation is higher than that of atpE translation. When the atpB 5′-UTR was replaced with lower efficiency 5′-UTRs, atpE translation was higher than atpB translation. Removal of the entire atpB 5′-UTR arrested atpB translation but atpE translation still proceeded. Introduction of a premature stop codon in the atpB cistron did not abolish atpE translation. These results indicate that atpE translation is independent of atpB translation. Mutation analysis showed that the atpE cistron possesses its own cis-element(s) for translation, located ∼25nt upstream from the start codon.
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U2 - 10.1093/nar/gkr644
DO - 10.1093/nar/gkr644
M3 - Article
C2 - 21846772
AN - SCOPUS:82255181553
SN - 0305-1048
VL - 39
SP - 9405
EP - 9412
JO - Nucleic acids research
JF - Nucleic acids research
IS - 21
ER -