| Full text | |
| Author(s): |
Leaden, Laura
[1]
;
Silva, Larissa G.
[1]
;
Ribeiro, Rodolfo A.
[1]
;
dos Santos, Naara M.
[1]
;
Lorenzetti, Alan P. R.
[2]
;
Alegria, Thiago G. P.
[3]
;
Schulz, Mariane L.
[4]
;
Medeiros, Marisa H. G.
[4]
;
Koide, Tie
[2]
;
Marques, V, Marilis
Total Authors: 10
|
| Affiliation: | [1] V, Univ Sao Paulo, Inst Ciencias Biomed, Dept Microbiol, Sao Paulo - Brazil
[2] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Bioquim & Imunol, Ribeirao Preto - Brazil
[3] Univ Sao Paulo, Inst Biociencias, Dept Genet & Biol Evolut, Sao Paulo - Brazil
[4] Univ Sao Paulo, Inst Quim, Dept Bioquim, Sao Paulo - Brazil
Total Affiliations: 4
|
| Document type: | Journal article |
| Source: | FRONTIERS IN MICROBIOLOGY; v. 9, AUG 28 2018. |
| Web of Science Citations: | 5 |
| Abstract | |
In C. crescentus, iron metabolism is mainly controlled by the transcription factor Fur (ferric uptake regulator). Iron-bound Fur represses genes related to iron uptake and can directly activate the expression of genes for iron-containing proteins. In this work, we used total RNA sequencing (RNA-seq) of wild type C. crescentus growing in minimal medium under iron limitation and a fur mutant strain to expand the known Fur regulon, and to identify novel iron-regulated genes. The RNA-seq of cultures treated with the iron chelator 2-2-dypiridyl (DP) allowed identifying 256 upregulated genes and 236 downregulated genes, being 176 and 204 newly identified, respectively. Sixteen transcription factors and seven sRNAs were upregulated in iron limitation, suggesting that the response to low iron triggers a complex regulatory network. Notably, lexA along with most of its target genes were upregulated, suggesting that DP treatment caused DNA damage, and the SOS DNA repair response was activated in a RecA-dependent manner, as confirmed by RT-qPCR. Fluorescence microscopy assays using an oxidation-sensitive dye showed that wild type cells in iron limitation and the fur mutant were under endogenous oxidative stress, and a direct measurement of cellular H2O2 showed that cells in iron-limited media present a higher amount of endogenous H2O2. A mutagenesis assay using the rpoB gene as a reporter showed that iron limitation led to an increase in the mutagenesis rate. These results showed that iron deficiency causes C. crescentus cells to suffer oxidative stress and to activate the SOS response, indicating an increase in DNA damage. (AU) | |
| FAPESP's process: | 16/06378-3 - Characterization of the DEAD-box RNA helicase CC1478 in Caulobacter crescentus and its regulation |
| Grantee: | Rodolfo Alvarenga Ribeiro |
| Support type: | Scholarships in Brazil - Master |
| FAPESP's process: | 15/07386-7 - Regulatory RNAs identification in response to iron availability and their mechanisms of action in Caulobacter crescentus |
| Grantee: | Laura Leaden |
| Support type: | Scholarships in Brazil - Post-Doctorate |
| FAPESP's process: | 14/04046-8 - Regulatory networks of bacterial stress response |
| Grantee: | Marilis Do Valle Marques |
| Support type: | Research Projects - Thematic Grants |
| FAPESP's process: | 17/03052-2 - Non-coding RNAs derived from insertion sequences in the halophilic archaeon Halobacterium salinarum NRC-1 |
| Grantee: | Alan Péricles Rodrigues Lorenzetti |
| Support type: | Scholarships in Brazil - Doctorate |
| FAPESP's process: | 15/21038-1 - The antisense transcriptome of the halophilic archaeon Halobacterium salinarum |
| Grantee: | Tie Koide |
| Support type: | Regular Research Grants |
| FAPESP's process: | 17/02127-9 - Characterization of iron transport systems in Caulobacter crescentus |
| Grantee: | Naara Marcondes dos Santos |
| Support type: | Scholarships in Brazil - Master |