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Comparative Analysis of Chloroplast psbD Promoters in Terrestrial Plants

The transcription of photosynthesis genes encoded by the plastid genome is mainly mediated by a prokaryotic-type RNA polymerase called plastid-encoded plastid RNA polymerase (PEP). Standard PEP-dependent promoters resemble bacterial sigma-70-type promoters containing the so-called -10 and -35 elemen...

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Autores principales: Shimmura, Shuichi, Nozoe, Mikio, Kitora, Shota, Kin, Satoko, Matsutani, Shigeru, Ishizaki, Yoko, Nakahira, Yoichi, Shiina, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508017/
https://www.ncbi.nlm.nih.gov/pubmed/28751898
http://dx.doi.org/10.3389/fpls.2017.01186
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author Shimmura, Shuichi
Nozoe, Mikio
Kitora, Shota
Kin, Satoko
Matsutani, Shigeru
Ishizaki, Yoko
Nakahira, Yoichi
Shiina, Takashi
author_facet Shimmura, Shuichi
Nozoe, Mikio
Kitora, Shota
Kin, Satoko
Matsutani, Shigeru
Ishizaki, Yoko
Nakahira, Yoichi
Shiina, Takashi
author_sort Shimmura, Shuichi
collection PubMed
description The transcription of photosynthesis genes encoded by the plastid genome is mainly mediated by a prokaryotic-type RNA polymerase called plastid-encoded plastid RNA polymerase (PEP). Standard PEP-dependent promoters resemble bacterial sigma-70-type promoters containing the so-called -10 and -35 elements. On the other hand, an unusual light- and stress-responsive promoter (psbD LRP) that is regulated by a 19-bp AAG-box immediately upstream of the -35 element has been mapped upstream of the psbD-psbC operon in some angiosperms. However, the occurrence of the AAG-box containing psbD LRP in plant evolution remains elusive. We have mapped the psbD promoters in eleven embryophytes at different evolutionary stages from liverworts to angiosperms. The psbD promoters were mostly mapped around 500–900 bp upstream of the psbD translational start sites, indicating that the psbD mRNAs have unusually long 5′-UTR extensions in common. The -10 elements of the psbD promoter are well-conserved in all embryophytes, but not the -35 elements. We found that the AAG-box sequences are highly conserved in angiosperms and gymnosperms except for gnetaceae plants. Furthermore, partial AAG-box-like sequences have been identified in the psbD promoters of some basal embryophytes such as moss, hornwort, and lycophyte, whereas liverwort has the standard PEP promoter without the AAG-box. These results suggest that the AAG-box sequences of the psbD LRP may have evolved from a primitive type of AAG-box of basal embryophytes. On the other hand, monilophytes (ferns) use another type of psbD promoter composed of a distinct cis-element upstream of the potential -35 element. Furthermore, we found that psbD expression is not regulated by light in gymnosperms or basal angiosperms, although they have the well-conserved AAG-box sequences. Thus, it is unlikely that acquisition of the AAG-box containing psbD promoter is directly associated with light-induced transcription of the psbD-psbC operon. Light- and stress-induced transcription may have evolved independently and multiple times during terrestrial plant evolution.
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spelling pubmed-55080172017-07-27 Comparative Analysis of Chloroplast psbD Promoters in Terrestrial Plants Shimmura, Shuichi Nozoe, Mikio Kitora, Shota Kin, Satoko Matsutani, Shigeru Ishizaki, Yoko Nakahira, Yoichi Shiina, Takashi Front Plant Sci Plant Science The transcription of photosynthesis genes encoded by the plastid genome is mainly mediated by a prokaryotic-type RNA polymerase called plastid-encoded plastid RNA polymerase (PEP). Standard PEP-dependent promoters resemble bacterial sigma-70-type promoters containing the so-called -10 and -35 elements. On the other hand, an unusual light- and stress-responsive promoter (psbD LRP) that is regulated by a 19-bp AAG-box immediately upstream of the -35 element has been mapped upstream of the psbD-psbC operon in some angiosperms. However, the occurrence of the AAG-box containing psbD LRP in plant evolution remains elusive. We have mapped the psbD promoters in eleven embryophytes at different evolutionary stages from liverworts to angiosperms. The psbD promoters were mostly mapped around 500–900 bp upstream of the psbD translational start sites, indicating that the psbD mRNAs have unusually long 5′-UTR extensions in common. The -10 elements of the psbD promoter are well-conserved in all embryophytes, but not the -35 elements. We found that the AAG-box sequences are highly conserved in angiosperms and gymnosperms except for gnetaceae plants. Furthermore, partial AAG-box-like sequences have been identified in the psbD promoters of some basal embryophytes such as moss, hornwort, and lycophyte, whereas liverwort has the standard PEP promoter without the AAG-box. These results suggest that the AAG-box sequences of the psbD LRP may have evolved from a primitive type of AAG-box of basal embryophytes. On the other hand, monilophytes (ferns) use another type of psbD promoter composed of a distinct cis-element upstream of the potential -35 element. Furthermore, we found that psbD expression is not regulated by light in gymnosperms or basal angiosperms, although they have the well-conserved AAG-box sequences. Thus, it is unlikely that acquisition of the AAG-box containing psbD promoter is directly associated with light-induced transcription of the psbD-psbC operon. Light- and stress-induced transcription may have evolved independently and multiple times during terrestrial plant evolution. Frontiers Media S.A. 2017-07-13 /pmc/articles/PMC5508017/ /pubmed/28751898 http://dx.doi.org/10.3389/fpls.2017.01186 Text en Copyright © 2017 Shimmura, Nozoe, Kitora, Kin, Matsutani, Ishizaki, Nakahira and Shiina. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Shimmura, Shuichi
Nozoe, Mikio
Kitora, Shota
Kin, Satoko
Matsutani, Shigeru
Ishizaki, Yoko
Nakahira, Yoichi
Shiina, Takashi
Comparative Analysis of Chloroplast psbD Promoters in Terrestrial Plants
title Comparative Analysis of Chloroplast psbD Promoters in Terrestrial Plants
title_full Comparative Analysis of Chloroplast psbD Promoters in Terrestrial Plants
title_fullStr Comparative Analysis of Chloroplast psbD Promoters in Terrestrial Plants
title_full_unstemmed Comparative Analysis of Chloroplast psbD Promoters in Terrestrial Plants
title_short Comparative Analysis of Chloroplast psbD Promoters in Terrestrial Plants
title_sort comparative analysis of chloroplast psbd promoters in terrestrial plants
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508017/
https://www.ncbi.nlm.nih.gov/pubmed/28751898
http://dx.doi.org/10.3389/fpls.2017.01186
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