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Fungal phytochrome chromophore biosynthesis at mitochondria
Mitochondria are essential organelles because of their function in energy conservation. Here, we show an involvement of mitochondria in phytochrome‐dependent light sensing in fungi. Phytochrome photoreceptors are found in plants, bacteria, and fungi and contain a linear, heme‐derived tetrapyrrole as...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447599/ https://www.ncbi.nlm.nih.gov/pubmed/34254350 http://dx.doi.org/10.15252/embj.2021108083 |
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author | Streng, Christian Hartmann, Jana Leister, Kai Krauß, Norbert Lamparter, Tilman Frankenberg‐Dinkel, Nicole Weth, Franco Bastmeyer, Martin Yu, Zhenzhong Fischer, Reinhard |
author_facet | Streng, Christian Hartmann, Jana Leister, Kai Krauß, Norbert Lamparter, Tilman Frankenberg‐Dinkel, Nicole Weth, Franco Bastmeyer, Martin Yu, Zhenzhong Fischer, Reinhard |
author_sort | Streng, Christian |
collection | PubMed |
description | Mitochondria are essential organelles because of their function in energy conservation. Here, we show an involvement of mitochondria in phytochrome‐dependent light sensing in fungi. Phytochrome photoreceptors are found in plants, bacteria, and fungi and contain a linear, heme‐derived tetrapyrrole as chromophore. Linearization of heme requires heme oxygenases (HOs) which reside inside chloroplasts in planta. Despite the poor degree of conservation of HOs, we identified two candidates in the fungus Alternaria alternata. Deletion of either one phenocopied phytochrome deletion. The two enzymes had a cooperative effect and physically interacted with phytochrome, suggesting metabolon formation. The metabolon was attached to the surface of mitochondria with a C‐terminal anchor (CTA) sequence in HoxA. The CTA was necessary and sufficient for mitochondrial targeting. The affinity of phytochrome apoprotein to HoxA was 57,000‐fold higher than the affinity of the holoprotein, suggesting a “kiss‐and‐go” mechanism for chromophore loading and a function of mitochondria as assembly platforms for functional phytochrome. Hence, two alternative approaches for chromophore biosynthesis and insertion into phytochrome evolved in plants and fungi. |
format | Online Article Text |
id | pubmed-8447599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84475992021-09-27 Fungal phytochrome chromophore biosynthesis at mitochondria Streng, Christian Hartmann, Jana Leister, Kai Krauß, Norbert Lamparter, Tilman Frankenberg‐Dinkel, Nicole Weth, Franco Bastmeyer, Martin Yu, Zhenzhong Fischer, Reinhard EMBO J Articles Mitochondria are essential organelles because of their function in energy conservation. Here, we show an involvement of mitochondria in phytochrome‐dependent light sensing in fungi. Phytochrome photoreceptors are found in plants, bacteria, and fungi and contain a linear, heme‐derived tetrapyrrole as chromophore. Linearization of heme requires heme oxygenases (HOs) which reside inside chloroplasts in planta. Despite the poor degree of conservation of HOs, we identified two candidates in the fungus Alternaria alternata. Deletion of either one phenocopied phytochrome deletion. The two enzymes had a cooperative effect and physically interacted with phytochrome, suggesting metabolon formation. The metabolon was attached to the surface of mitochondria with a C‐terminal anchor (CTA) sequence in HoxA. The CTA was necessary and sufficient for mitochondrial targeting. The affinity of phytochrome apoprotein to HoxA was 57,000‐fold higher than the affinity of the holoprotein, suggesting a “kiss‐and‐go” mechanism for chromophore loading and a function of mitochondria as assembly platforms for functional phytochrome. Hence, two alternative approaches for chromophore biosynthesis and insertion into phytochrome evolved in plants and fungi. John Wiley and Sons Inc. 2021-07-13 2021-09-01 /pmc/articles/PMC8447599/ /pubmed/34254350 http://dx.doi.org/10.15252/embj.2021108083 Text en © 2021 The Authors. Published under the terms of the CC BY NC ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Articles Streng, Christian Hartmann, Jana Leister, Kai Krauß, Norbert Lamparter, Tilman Frankenberg‐Dinkel, Nicole Weth, Franco Bastmeyer, Martin Yu, Zhenzhong Fischer, Reinhard Fungal phytochrome chromophore biosynthesis at mitochondria |
title | Fungal phytochrome chromophore biosynthesis at mitochondria |
title_full | Fungal phytochrome chromophore biosynthesis at mitochondria |
title_fullStr | Fungal phytochrome chromophore biosynthesis at mitochondria |
title_full_unstemmed | Fungal phytochrome chromophore biosynthesis at mitochondria |
title_short | Fungal phytochrome chromophore biosynthesis at mitochondria |
title_sort | fungal phytochrome chromophore biosynthesis at mitochondria |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447599/ https://www.ncbi.nlm.nih.gov/pubmed/34254350 http://dx.doi.org/10.15252/embj.2021108083 |
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