Feb 4, 2014

BCKDK regulates the TCA cycle through PDC to ensure embryonic development in the absence of PDK family

BioRxiv : the Preprint Server for Biology
Hong-Dong LiElazar Zelzer

Abstract

Pyruvate dehydrogenase kinase family of enzymes (PDK1-4) are central negative regulators of the TCA cycle by phosphorylating the rate-limiting multi-enzyme pyruvate dehydrogenase complex (PDC). Here, we show that the PDK family is dispensable for murine embryonic development and that BCKDK serves as a compensatory mechanism for PDKs by inactivating PDC. To study the role of Pdk family in vivo, we knocked out all four genes one by one. Surprisingly, Pdk total KO mouse embryos developed and were born in the expected ratio. Postnatally, these mice died by day four due to hypoglycemia or ketoacidosis, as confirmed by deep metabolic profiling. Looking for the mechanism that enables development in the absence of Pdks, we found that PDC site 2 (S300) was phosphorylated in these embryos, suggesting that another kinase compensates for the PDK family. Bioinformatic analysis predicted brunch chain ketoacid dehydrogenase kinase (Bckdk), a key regulator in the catabolism of branched chain amino acids (BCAA), as a candidate. Knockout of both Bckdk and the entire Pdk family led to loss of PDC phosphorylation on S300 and early embryonic lethality which firmly establish the role of BCKDK in the regulation of PDC. Altogether, this work demonstra...Continue Reading

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Mentioned in this Paper

Classification
Genes
Literature
Gene Function
Analysis

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