2020
DOI: 10.1016/j.micpath.2020.104281
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Nitrogen Catabolite Repression in members of Paracoccidioides complex

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Cited by 9 publications
(9 citation statements)
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“…RNA-seq analysis under SYA+N condition showed that MaNCP1 involved in multiple metabolic pathways, the amino acid permease MAC_09768, a DEG, is homologous to the amino acid permease GAP1 in S. cerevisiae, which is regulated by the Gln3 and Gat1 in S. cerevisiae [44]. It has been reported that the GATA transcription factor AreA, which function is similar to Gln3/Gat1, interacts with Gap1 in A. nidulans [37]. In this study, we confirmed that MaAreA was a direct target gene of MaNCP1.…”
Section: Discussionmentioning
confidence: 99%
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“…RNA-seq analysis under SYA+N condition showed that MaNCP1 involved in multiple metabolic pathways, the amino acid permease MAC_09768, a DEG, is homologous to the amino acid permease GAP1 in S. cerevisiae, which is regulated by the Gln3 and Gat1 in S. cerevisiae [44]. It has been reported that the GATA transcription factor AreA, which function is similar to Gln3/Gat1, interacts with Gap1 in A. nidulans [37]. In this study, we confirmed that MaAreA was a direct target gene of MaNCP1.…”
Section: Discussionmentioning
confidence: 99%
“…Further analysis revealed that MAC_09768 (Figure 5D), a DEG involved in the RNA-seq data, encoding an amino acid permease, which was homologous to Saccharomyces cerevisiae amino acid permease GAP1 (NP_012965.3). GAP1 is an important marker protein to respond to NCR and a main regulator of yeast plasma membrane in nitrogen starvation condition [35,36], and could interact with AreA in A. nidulans [37]. Therefore, we reasoned that the involvement of MaNCP1 in regulating conidiation may be related to the NCR pathway.…”
Section: Transcriptomic Insights Into Pleiotropic Effects Of Mancp1mentioning
confidence: 99%
“…The yeast cells were then incubated in Brain Heart Infusion (BHI) medium supplemented with 4% (w/v) glucose at 36 • C under rotation for 48 h. The cells were centrifuged at 1900× g for 10 min at 4 • C and washed twice in phosphate-buffered saline (PBS). The yeast (2 × 10 6 cells/mL), was inoculated under NCR conditions, as described by Cruz-Leite et al [41]. In brief, the yeast cells were grown in Yeast Nitrogen Base (YNB) without amino acids and ammonium sulfate (Sigma-Aldrich ® , St. Louis, MO, USA), supplemented with either 10 mM glutamine or 10 mM proline nitrogen sources plus 2% glucose (w/v) for 48 h. Glutamine, a preferential nitrogen source, triggers repressive NCR conditions, while proline, a non-preferential nitrogen source, triggers alleviation of NCR [14].…”
Section: P Lutzii Growth Conditionsmentioning
confidence: 99%
“…The relative expression levels of the NCR genes formamidase (PAAG_03333), arginase (PAAG_01969), urease (PAAG_00954) and γ-glutamyl transpeptidase (PAAG_06130) were calculated using the standard curve method for relative quantification [43]. The tubulin gene (PAAG_03031) was used as an endogenous control, as described by Cruz-Leite et al [41]. Student's t-test was applied, and p ≤ 0.05 was considered as statistically significant.…”
Section: Rna Extraction and Quantitative Real-time Rt-qpcr Analysismentioning
confidence: 99%
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