2018
DOI: 10.1186/s13104-018-3364-z
|View full text |Cite
|
Sign up to set email alerts
|

Concurrent interactome and metabolome analysis reveals role of AKT1 in central carbon metabolism

Abstract: ObjectiveSignal transduction not only initiates entry into the cell cycle, but also reprograms the cell’s metabolism. To control abnormalities in cell proliferation, both the aspects should be taken care of, thus pleiotropic signaling molecules are considered as crucial modulators. Considering this, we investigated the role of AKT1 in central carbon metabolism. The role of AKT1 has already been established in the process of cell cycle, but its contribution to the central carbon metabolism is sparsely studied.R… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2019
2019
2023
2023

Publication Types

Select...
3
1

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(2 citation statements)
references
References 18 publications
0
2
0
Order By: Relevance
“…In order to analyze the metabolic state of Mtb depleted with DNA gyrase expression, we estimated the levels of metabolites by LC-MS/MS, as described in the materials and methods. Metabolites in both the control and gyr(-) were quantified by using concentration-dependent standard curves for each metabolite as described earlier (Gupta et al, 2018). Those small molecules which exhibit minimal variation ( P < 0.05) in six biological samples were examined for fold-change in their levels between the two strains (Supplementary Dataset 4).…”
Section: Resultsmentioning
confidence: 99%
“…In order to analyze the metabolic state of Mtb depleted with DNA gyrase expression, we estimated the levels of metabolites by LC-MS/MS, as described in the materials and methods. Metabolites in both the control and gyr(-) were quantified by using concentration-dependent standard curves for each metabolite as described earlier (Gupta et al, 2018). Those small molecules which exhibit minimal variation ( P < 0.05) in six biological samples were examined for fold-change in their levels between the two strains (Supplementary Dataset 4).…”
Section: Resultsmentioning
confidence: 99%
“…22,23 Glucose carbon entry into the TCA cycle via PDH was also inhibited by uprosertib, consistent with previous work that suggests a direct interaction between PDH subunit B and AKT1 and that silencing of AKT1 could reduce PDH flux from 13 C labelled glucose. 35 By contrast exogenous lactate incorporation into citrate was maintained in cells treated with uprosertib. Furthermore, lactic acidosis stimulated an increase in respiration and respiratory capacity in our cell models.…”
Section: Discussionmentioning
confidence: 98%