Cargando…
RcLS2F – A Novel Fungal Class 1 KDAC Co-repressor Complex in Aspergillus nidulans
The fungal class 1 lysine deacetylase (KDAC) RpdA is a promising target for prevention and treatment of invasive fungal infection. RpdA is essential for survival of the most common air-borne mold pathogen Aspergillus fumigatus and the model organism Aspergillus nidulans. In A. nidulans, RpdA depleti...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7010864/ https://www.ncbi.nlm.nih.gov/pubmed/32117098 http://dx.doi.org/10.3389/fmicb.2020.00043 |
_version_ | 1783495960591073280 |
---|---|
author | Bauer, Ingo Gross, Silke Merschak, Petra Kremser, Leopold Karahoda, Betim Bayram, Özlem Sarikaya Abt, Beate Binder, Ulrike Gsaller, Fabio Lindner, Herbert Bayram, Özgür Brosch, Gerald Graessle, Stefan |
author_facet | Bauer, Ingo Gross, Silke Merschak, Petra Kremser, Leopold Karahoda, Betim Bayram, Özlem Sarikaya Abt, Beate Binder, Ulrike Gsaller, Fabio Lindner, Herbert Bayram, Özgür Brosch, Gerald Graessle, Stefan |
author_sort | Bauer, Ingo |
collection | PubMed |
description | The fungal class 1 lysine deacetylase (KDAC) RpdA is a promising target for prevention and treatment of invasive fungal infection. RpdA is essential for survival of the most common air-borne mold pathogen Aspergillus fumigatus and the model organism Aspergillus nidulans. In A. nidulans, RpdA depletion induced production of previously unknown small bioactive substances. As known from yeasts and mammals, class 1 KDACs act as components of multimeric protein complexes, which previously was indicated also for A. nidulans. Composition of these complexes, however, remained obscure. In this study, we used tandem affinity purification to characterize different RpdA complexes and their composition in A. nidulans. In addition to known class 1 KDAC interactors, we identified a novel RpdA complex, which was termed RcLS2F. It contains ScrC, previously described as suppressor of the transcription factor CrzA, as well as the uncharacterized protein FscA. We show that recruitment of FscA depends on ScrC and we provide clear evidence that ΔcrzA suppression by ScrC depletion is due to a lack of transcriptional repression caused by loss of the novel RcLS2F complex. Moreover, RcLS2F is essential for sexual development and engaged in an autoregulatory feed-back loop. |
format | Online Article Text |
id | pubmed-7010864 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70108642020-02-28 RcLS2F – A Novel Fungal Class 1 KDAC Co-repressor Complex in Aspergillus nidulans Bauer, Ingo Gross, Silke Merschak, Petra Kremser, Leopold Karahoda, Betim Bayram, Özlem Sarikaya Abt, Beate Binder, Ulrike Gsaller, Fabio Lindner, Herbert Bayram, Özgür Brosch, Gerald Graessle, Stefan Front Microbiol Microbiology The fungal class 1 lysine deacetylase (KDAC) RpdA is a promising target for prevention and treatment of invasive fungal infection. RpdA is essential for survival of the most common air-borne mold pathogen Aspergillus fumigatus and the model organism Aspergillus nidulans. In A. nidulans, RpdA depletion induced production of previously unknown small bioactive substances. As known from yeasts and mammals, class 1 KDACs act as components of multimeric protein complexes, which previously was indicated also for A. nidulans. Composition of these complexes, however, remained obscure. In this study, we used tandem affinity purification to characterize different RpdA complexes and their composition in A. nidulans. In addition to known class 1 KDAC interactors, we identified a novel RpdA complex, which was termed RcLS2F. It contains ScrC, previously described as suppressor of the transcription factor CrzA, as well as the uncharacterized protein FscA. We show that recruitment of FscA depends on ScrC and we provide clear evidence that ΔcrzA suppression by ScrC depletion is due to a lack of transcriptional repression caused by loss of the novel RcLS2F complex. Moreover, RcLS2F is essential for sexual development and engaged in an autoregulatory feed-back loop. Frontiers Media S.A. 2020-02-04 /pmc/articles/PMC7010864/ /pubmed/32117098 http://dx.doi.org/10.3389/fmicb.2020.00043 Text en Copyright © 2020 Bauer, Gross, Merschak, Kremser, Karahoda, Sarikaya Bayram, Abt, Binder, Gsaller, Lindner, Bayram, Brosch and Graessle. 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) and the copyright owner(s) 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 | Microbiology Bauer, Ingo Gross, Silke Merschak, Petra Kremser, Leopold Karahoda, Betim Bayram, Özlem Sarikaya Abt, Beate Binder, Ulrike Gsaller, Fabio Lindner, Herbert Bayram, Özgür Brosch, Gerald Graessle, Stefan RcLS2F – A Novel Fungal Class 1 KDAC Co-repressor Complex in Aspergillus nidulans |
title | RcLS2F – A Novel Fungal Class 1 KDAC Co-repressor Complex in Aspergillus nidulans |
title_full | RcLS2F – A Novel Fungal Class 1 KDAC Co-repressor Complex in Aspergillus nidulans |
title_fullStr | RcLS2F – A Novel Fungal Class 1 KDAC Co-repressor Complex in Aspergillus nidulans |
title_full_unstemmed | RcLS2F – A Novel Fungal Class 1 KDAC Co-repressor Complex in Aspergillus nidulans |
title_short | RcLS2F – A Novel Fungal Class 1 KDAC Co-repressor Complex in Aspergillus nidulans |
title_sort | rcls2f – a novel fungal class 1 kdac co-repressor complex in aspergillus nidulans |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7010864/ https://www.ncbi.nlm.nih.gov/pubmed/32117098 http://dx.doi.org/10.3389/fmicb.2020.00043 |
work_keys_str_mv | AT baueringo rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans AT grosssilke rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans AT merschakpetra rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans AT kremserleopold rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans AT karahodabetim rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans AT bayramozlemsarikaya rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans AT abtbeate rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans AT binderulrike rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans AT gsallerfabio rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans AT lindnerherbert rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans AT bayramozgur rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans AT broschgerald rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans AT graesslestefan rcls2fanovelfungalclass1kdaccorepressorcomplexinaspergillusnidulans |