Author
Listed:
- Ilke Sen
(Karolinska Institute
Karolinska Institute
University Medical Center Groningen (UMCG), University of Groningen)
- Xin Zhou
(Karolinska Institute
Karolinska Institute)
- Alexey Chernobrovkin
(Karolinska Institute)
- Nataly Puerta-Cavanzo
(University Medical Center Groningen (UMCG), University of Groningen)
- Takaharu Kanno
(Karolinska Institute
Karolinska Institute)
- Jérôme Salignon
(Karolinska Institute
Karolinska Institute)
- Andrea Stoehr
(Karolinska Institute
Karolinska Institute)
- Xin-Xuan Lin
(Karolinska Institute
Karolinska Institute)
- Bora Baskaner
(Karolinska Institute)
- Simone Brandenburg
(University Medical Center Groningen (UMCG), University of Groningen)
- Camilla Björkegren
(Karolinska Institute
Karolinska Institute)
- Roman A. Zubarev
(Karolinska Institute)
- Christian G. Riedel
(Karolinska Institute
Karolinska Institute
University Medical Center Groningen (UMCG), University of Groningen)
Abstract
In C. elegans, the conserved transcription factor DAF-16/FOXO is a powerful aging regulator, relaying dire conditions into expression of stress resistance and longevity promoting genes. For some of these functions, including low insulin/IGF signaling (IIS), DAF-16 depends on the protein SMK-1/SMEK, but how SMK-1 exerts this role has remained unknown. We show that SMK-1 functions as part of a specific Protein Phosphatase 4 complex (PP4SMK-1). Loss of PP4SMK-1 hinders transcriptional initiation at several DAF-16-activated genes, predominantly by impairing RNA polymerase II recruitment to their promoters. Search for the relevant substrate of PP4SMK-1 by phosphoproteomics identified the conserved transcriptional regulator SPT-5/SUPT5H, whose knockdown phenocopies the loss of PP4SMK-1. Phosphoregulation of SPT-5 is known to control transcriptional events such as elongation and termination. Here we also show that transcription initiating events are influenced by the phosphorylation status of SPT-5, particularly at DAF-16 target genes where transcriptional initiation appears rate limiting, rendering PP4SMK-1 crucial for many of DAF-16’s physiological roles.
Suggested Citation
Ilke Sen & Xin Zhou & Alexey Chernobrovkin & Nataly Puerta-Cavanzo & Takaharu Kanno & Jérôme Salignon & Andrea Stoehr & Xin-Xuan Lin & Bora Baskaner & Simone Brandenburg & Camilla Björkegren & Roman A, 2020.
"DAF-16/FOXO requires Protein Phosphatase 4 to initiate transcription of stress resistance and longevity promoting genes,"
Nature Communications, Nature, vol. 11(1), pages 1-17, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-019-13931-7
DOI: 10.1038/s41467-019-13931-7
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