Cross regulation between Candida albicans catalytic and regulatory subunits of protein kinase A
In the pathogen Candida albicans protein kinase A [PKA] catalytic subunit is encoded by two genes TPK1 and TPK2 and the regulatory subunit by one gene, BCY1. PKA mediates several cellular processes such as cell cycle regulation and the yeast to hyphae transition, a key factor for C. albicans virulen...
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| Acceso en línea: | http://ri.agro.uba.ar/files/intranet/articulo/2012Giacometti.pdf LINK AL EDITOR |
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| 245 | 1 | 0 | |a Cross regulation between Candida albicans catalytic and regulatory subunits of protein kinase A |
| 520 | |a In the pathogen Candida albicans protein kinase A [PKA] catalytic subunit is encoded by two genes TPK1 and TPK2 and the regulatory subunit by one gene, BCY1. PKA mediates several cellular processes such as cell cycle regulation and the yeast to hyphae transition, a key factor for C. albicans virulence. The catalytic isoforms Tpk1p and Tpk2p share redundant functions in vegetative growth and hyphal development, though they differentially regulate glycogen metabolism, the stress response pathway and pseudohyphal formation. In Saccharomyces cerevisiae it was earlier reported that BCY1 overexpression not only increased the amount of TPK3 mRNA but also its catalytic activity. In C. albicans a significant decrease in Bcy1p expression levels was already observed in tpk2delta null strains. In this work we showed that the upregulation in Bcy1p expression was observed in a set of strains having a TPK1 or TPK2 allele reintegrated in its own locus, as well as in strains expressing the TPKs under the control of the constitutive ACT1 promoter. To confirm the cross regulation event between Bcy1p and Tpkp expression we generated a mutant strain with the lowest PKA activity carrying one TPK1 and a unique BCY1 allele with the aim to obtain two derived strains in which BCY1 or TPK1 were placed under their own promoters inserted in the RPS10 neutral locus. We found that placing one copy of BCY1 upregulated the levels of Tpk1p and its catalytic activity; while TPK1 insertion led to an increase in BCY1 mRNA, Bcy1p and in a high cAMP binding activity. Our results suggest that C. albicans cells were able to compensate for the increased levels of either Tpk1p or Tpk2p subunits with a corresponding elevation of Bcy1 protein levels and vice versa, implying a tightly regulated mechanism to balance holoenzyme formation. | ||
| 653 | 0 | |a CAMP BINDING ACTIVITY | |
| 653 | 0 | |a CANDIDA ALBICANS | |
| 653 | 0 | |a PKA ACTIVITY | |
| 653 | 0 | |a TRANSCRIPTIONAL CROSS REGULATION | |
| 653 | 0 | |a CYCLIC AMP | |
| 653 | 0 | |a CYCLIC AMP DEPENDENT PROTEIN KINASE | |
| 653 | 0 | |a HOLOENZYME | |
| 653 | 0 | |a MESSENGER RNA | |
| 653 | 0 | |a ACT1 GENE | |
| 653 | 0 | |a ALLELE | |
| 653 | 0 | |a BCY1 GENE | |
| 653 | 0 | |a CATALYST | |
| 653 | 0 | |a CONTROLLED STUDY | |
| 653 | 0 | |a ENZYME ACTIVITY | |
| 653 | 0 | |a ENZYME REGULATION | |
| 653 | 0 | |a FUNGAL GENE | |
| 653 | 0 | |a FUNGAL STRAIN | |
| 653 | 0 | |a GENE EXPRESSION | |
| 653 | 0 | |a GENE INSERTION | |
| 653 | 0 | |a GENE LOCUS | |
| 653 | 0 | |a HETEROZYGOSITY | |
| 653 | 0 | |a NONHUMAN | |
| 653 | 0 | |a PLASMID | |
| 653 | 0 | |a PROMOTER REGION | |
| 653 | 0 | |a PROTEIN BINDING | |
| 653 | 0 | |a TPK1 GENE | |
| 653 | 0 | |a TPK2 GENE | |
| 653 | 0 | |a TRANSCRIPTION REGULATION | |
| 653 | 0 | |a UPREGULATION | |
| 653 | 0 | |a CYCLIC AMP-DEPENDENT PROTEIN KINASES | |
| 653 | 0 | |a GENE DELETION | |
| 653 | 0 | |a GENE EXPRESSION PROFILING | |
| 653 | 0 | |a GENE EXPRESSION REGULATION, FUNGAL | |
| 653 | 0 | |a MUTANT PROTEINS | |
| 653 | 0 | |a SACCHAROMYCES CEREVISIAE | |
| 700 | 1 | |9 68244 |a Giacometti, Romina | |
| 700 | 1 | |9 66853 |a Kronberg, María Florencia | |
| 700 | 1 | |9 69374 |a Biondi, Ricardo M. | |
| 700 | 1 | |a Hernández Agramonte, Ignacio |9 38543 | |
| 700 | 1 | |9 48345 |a Passeron, Susana | |
| 773 | |t Fungal Genetics and Biology |g Vol.49, no.1 (2012), p.74-85 | ||
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| 900 | |a ^tCross regulation between Candida albicans catalytic and regulatory subunits of protein kinase A | ||
| 900 | |a ^aGiacometti^bR. | ||
| 900 | |a ^aKronberg^bF. | ||
| 900 | |a ^aBiondi^bR.M. | ||
| 900 | |a ^aHernández^bA.I. | ||
| 900 | |a ^aPasseron^bS. | ||
| 900 | |a ^aGiacometti^bR. | ||
| 900 | |a ^aKronberg^bF. | ||
| 900 | |a ^aBiondi^bR. M. | ||
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| 900 | |a ^aPasseron^bS. | ||
| 900 | |a ^aGiacometti^bR.^tCátedra de MicrobiologÃa, Facultad de AgronomÃa, Universidad de Buenos Aires, INBA-CONICET, Avda. San MartÃn 4453, C1417DSE Buenos Aires, Argentina | ||
| 900 | |a ^aKronberg^bF.^tResearch Group PhosphoSites, Medizinische Klinik I, Universitätsklinikum Frankfurt, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany | ||
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| 900 | |a ^aHernández^bA.I. | ||
| 900 | |a ^aPasseron^bS. | ||
| 900 | |a ^tFungal Genetics and Biology^cFungal Genet. Biol. | ||
| 900 | |a en | ||
| 900 | |a 74 | ||
| 900 | |a ^i | ||
| 900 | |a Vol. 49, no. 1 | ||
| 900 | |a 85 | ||
| 900 | |a CAMP BINDING ACTIVITY | ||
| 900 | |a CANDIDA ALBICANS | ||
| 900 | |a PKA ACTIVITY | ||
| 900 | |a TRANSCRIPTIONAL CROSS REGULATION | ||
| 900 | |a CYCLIC AMP | ||
| 900 | |a CYCLIC AMP DEPENDENT PROTEIN KINASE | ||
| 900 | |a HOLOENZYME | ||
| 900 | |a MESSENGER RNA | ||
| 900 | |a ACT1 GENE | ||
| 900 | |a ALLELE | ||
| 900 | |a BCY1 GENE | ||
| 900 | |a CATALYST | ||
| 900 | |a CONTROLLED STUDY | ||
| 900 | |a ENZYME ACTIVITY | ||
| 900 | |a ENZYME REGULATION | ||
| 900 | |a FUNGAL GENE | ||
| 900 | |a FUNGAL STRAIN | ||
| 900 | |a GENE EXPRESSION | ||
| 900 | |a GENE INSERTION | ||
| 900 | |a GENE LOCUS | ||
| 900 | |a HETEROZYGOSITY | ||
| 900 | |a NONHUMAN | ||
| 900 | |a PLASMID | ||
| 900 | |a PROMOTER REGION | ||
| 900 | |a PROTEIN BINDING | ||
| 900 | |a TPK1 GENE | ||
| 900 | |a TPK2 GENE | ||
| 900 | |a TRANSCRIPTION REGULATION | ||
| 900 | |a UPREGULATION | ||
| 900 | |a CYCLIC AMP-DEPENDENT PROTEIN KINASES | ||
| 900 | |a GENE DELETION | ||
| 900 | |a GENE EXPRESSION PROFILING | ||
| 900 | |a GENE EXPRESSION REGULATION, FUNGAL | ||
| 900 | |a MUTANT PROTEINS | ||
| 900 | |a SACCHAROMYCES CEREVISIAE | ||
| 900 | |a In the pathogen Candida albicans protein kinase A [PKA] catalytic subunit is encoded by two genes TPK1 and TPK2 and the regulatory subunit by one gene, BCY1. PKA mediates several cellular processes such as cell cycle regulation and the yeast to hyphae transition, a key factor for C. albicans virulence. The catalytic isoforms Tpk1p and Tpk2p share redundant functions in vegetative growth and hyphal development, though they differentially regulate glycogen metabolism, the stress response pathway and pseudohyphal formation. In Saccharomyces cerevisiae it was earlier reported that BCY1 overexpression not only increased the amount of TPK3 mRNA but also its catalytic activity. In C. albicans a significant decrease in Bcy1p expression levels was already observed in tpk2delta null strains. In this work we showed that the upregulation in Bcy1p expression was observed in a set of strains having a TPK1 or TPK2 allele reintegrated in its own locus, as well as in strains expressing the TPKs under the control of the constitutive ACT1 promoter. To confirm the cross regulation event between Bcy1p and Tpkp expression we generated a mutant strain with the lowest PKA activity carrying one TPK1 and a unique BCY1 allele with the aim to obtain two derived strains in which BCY1 or TPK1 were placed under their own promoters inserted in the RPS10 neutral locus. We found that placing one copy of BCY1 upregulated the levels of Tpk1p and its catalytic activity; while TPK1 insertion led to an increase in BCY1 mRNA, Bcy1p and in a high cAMP binding activity. Our results suggest that C. albicans cells were able to compensate for the increased levels of either Tpk1p or Tpk2p subunits with a corresponding elevation of Bcy1 protein levels and vice versa, implying a tightly regulated mechanism to balance holoenzyme formation. | ||
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