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NtcA is responsible for accumulation of the small isoform of ferredoxin:NADP oxidoreductase
In several cyanobacteria, petH, the gene encoding ferredoxin:NADP oxidoreductase (FNR), is transcribed from at least two promoters depending on growth conditions. Two transcripts (short and long) are translated from two different translation initiation sites, resulting in two isoforms (large and sma...
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Published in: | Microbiology (Society for General Microbiology) 2014-04, Vol.160 (Pt 4), p.789-794 |
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container_issue | Pt 4 |
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container_title | Microbiology (Society for General Microbiology) |
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creator | Omairi-Nasser, Amin Galmozzi, Carla V Latifi, Amel Muro-Pastor, M Isabel Ajlani, Ghada |
description | In several cyanobacteria, petH, the gene encoding ferredoxin:NADP oxidoreductase (FNR), is transcribed from at least two promoters depending on growth conditions. Two transcripts (short and long) are translated from two different translation initiation sites, resulting in two isoforms (large and small, respectively). Here, we show that in Synechocystis PCC6803 the global transcriptional regulator NtcA activates transcription from the distal petH promoter. Modification of the NtcA-binding site prevents NtcA binding to the promoter in vitro and abolishes accumulation of the small isoform of FNR in vivo. We also demonstrate that a similar petH transcription and translation regime occurs in other cyanobacteria. The conditions under which this system operates provide hints for the function of each FNR isoform. |
doi_str_mv | 10.1099/mic.0.076042-0 |
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subjects | Bacterial Proteins - metabolism Binding Sites DNA Mutational Analysis DNA-Binding Proteins - metabolism Ferredoxin-NADP Reductase - metabolism Flavoproteins - metabolism Gene Expression Gene Expression Regulation, Bacterial Promoter Regions, Genetic Protein Isoforms - metabolism Synechocystis - enzymology Synechocystis - genetics Transcription Factors - metabolism Transcription, Genetic |
title | NtcA is responsible for accumulation of the small isoform of ferredoxin:NADP oxidoreductase |
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