Peer review in Salt-inducible kinases mediate nutrient-sensing to link dietary sugar and tumorigenesis in Drosophila

Decision letter
Author response

Decision letter

Duojia Pan

Reviewing Editor; Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, United States

eLife posts the editorial decision letter and author response on a selection of the published articles (subject to the approval of the authors). An edited version of the letter sent to the authors after peer review is shown, indicating the substantive concerns or comments; minor concerns are not usually shown. Reviewers have the opportunity to discuss the decision before the letter is sent (see review process). Similarly, the author response typically shows only responses to the major concerns raised by the reviewers.

Thank you for submitting your work entitled “Salt-Inducible Kinases Mediate Nutrient-Sensing To Link Dietary Sugar and Tumorigenesis in Drosophila” for peer review at eLife. Your submission has been favorably evaluated by Tony Hunter (Senior Editor) and two reviewers, one of whom is a member of our Board of Reviewing Editors.

The reviewers have discussed the reviews with one another and the Reviewing editor has drafted this decision to help you prepare a revised submission.

The work addresses the link between diabetes/obesity and increased tumour susceptibility. In previous work, the authors have established a Drosophila model in which a combination of dietary glucose and Ras + Src oncogenes can lead to enhanced tumorigenesis by inducing the expression of Wnt and Insulin Receptor. In the current manuscript, the authors identify the Hippo pathway effector Yorkie as an essential mediator of Wnt induction in the tumors. Mechanistically, the authors show that activation of Yki is due to activation of Salt Inducible Kinases (SIKs) by Ras + Src + dietary glucose. Overall, the study is well conducted and clearly presented, and will be of broad interest to the cancer, diabetes and developmental growth control communities. The authors have identified a potentially important mechanism by which nutrients cooperate oncogenes to drive tumorigenesis. Furthermore, this represents the first clear demonstration that the Hippo pathway is regulated by metabolism.

Essential revisions:

1) Some additional insight into how SIK is activated in response to HDS would strengthen the study. Is it Akt-dependent, as is suggested by the strong activation of Akt by HDS in their previous study (Hirabayashi et al., Cell 2013)? This could be addressed by activating Akt in normal diet or RNAi depletion of Akt in HDS.

2) Please include statistics (Reviewer 1), the molecular weight markers and scale bars (Reviewer 2) in the revision.

https://doi.org/10.7554/eLife.08501.014

Author response

Essential revisions:

Previous studies in mammals and Drosophila have shown that SIKs are activated by Akt. To assess the role of Akt in activation of SIKs in our model, we used a hypomorphic allele of akt (akt⁰⁴²²⁶) and established ras1^G12V;csk^−/−,akt^hypo/hypo and inr^CA,ras1^G12V;csk^−/−,akt^hypo/hypo lines. Reducing Akt-activity in ras1^G12V;csk^−/− animals raised on a HDS or in inr^CA,ras1^G12V;csk^−/− animals raised on a control diet both suppressed tumor growth and activation of SIKs as assessed by Western-blot analysis using anti-phospho Sav antibody (Figure 3–figure supplement 1). Therefore, together with the evidence that increased insulin signaling in Ras/Src-activated cells (inr^CA,ras1^G12V;csk^−/−) promotes SIK activity (Figure 3A), we now clearly demonstrate that the activation of SIKs in the eye tissues of ras1^G12V;csk^−/− larvae fed HDS and in inr^CA, ras1^G12V;csk^−/− animals fed a control diet are mediated by Akt.

2) Please include statistics (Reviewer 1), the molecular weight markers and scale bars (Reviewer 2) in the revision.

We have provided statistics for the quantification in Figures 1H, 2I and 3J, molecular weight markers in all Western-blot data and scale bars in all immunofluorescence data.

https://doi.org/10.7554/eLife.08501.015