Regulation of the somatotropic axis by MYC-mediated miRNA repression

The transcription factor MYC is overexpressed in many human cancers and has a significant causal role in tumor incidence and progression. In contrast, Myc+/− heterozygous mice, which have decreased MYC expression, exhibit a 10–20% increase in lifespan and a decreased incidence or progression of seve...

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Main Authors: Anna P. Petrashen, Andrew D. Verdesca, Jill A. Kreiling, John M. Sedivy
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-10-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2023.1269860/full
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author Anna P. Petrashen
Andrew D. Verdesca
Jill A. Kreiling
John M. Sedivy
author_facet Anna P. Petrashen
Andrew D. Verdesca
Jill A. Kreiling
John M. Sedivy
author_sort Anna P. Petrashen
collection DOAJ
description The transcription factor MYC is overexpressed in many human cancers and has a significant causal role in tumor incidence and progression. In contrast, Myc+/− heterozygous mice, which have decreased MYC expression, exhibit a 10–20% increase in lifespan and a decreased incidence or progression of several age-related diseases. Myc heterozygous mice were also reported to have decreased mTOR and IGF1 signaling, two pathways whose reduced activity is associated with longevity in diverse species. Given MYC’s downstream role in these pathways, the downregulation of mTOR and IGF1 signaling in Myc heterozygotes suggests the presence of feedback loops within this regulatory network. In this communication we provide further evidence that the reduction of Myc expression in Myc+/− heterozygous mice provokes a female-specific decrease in circulating IGF1 as well as a reduction of IGF1 protein in the liver. In particular, reduced Myc expression led to upregulation of miRNAs that target the Igf1 transcript, thereby inhibiting its translation and leading to decreased IGF1 protein levels. Using Argonaute (AGO)-CLIP-sequencing we found enrichment of AGO binding in the Igf1 transcript at the target sites of let-7, miR-122, and miR-29 in female, but not male Myc heterozygotes. Upregulation of the liver-specific miR-122 in primary hepatocytes in culture and in vivo in mice resulted in significant downregulation of IGF1 protein, but not mRNA. Reduced levels of IGF1 increased GH production in the pituitary through a well-documented negative-feedback relationship. In line with this, we found that IGF1 levels in bone (where miR-122 is not expressed) were unchanged, consistent with the decreased incidence of osteoporosis in female Myc heterozygotes, despite decreased circulating IGF1.
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spelling doaj.art-821f2ca0d3094bd79ffe9c58d4f933422023-10-16T15:57:15ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2023-10-011110.3389/fcell.2023.12698601269860Regulation of the somatotropic axis by MYC-mediated miRNA repressionAnna P. PetrashenAndrew D. VerdescaJill A. KreilingJohn M. SedivyThe transcription factor MYC is overexpressed in many human cancers and has a significant causal role in tumor incidence and progression. In contrast, Myc+/− heterozygous mice, which have decreased MYC expression, exhibit a 10–20% increase in lifespan and a decreased incidence or progression of several age-related diseases. Myc heterozygous mice were also reported to have decreased mTOR and IGF1 signaling, two pathways whose reduced activity is associated with longevity in diverse species. Given MYC’s downstream role in these pathways, the downregulation of mTOR and IGF1 signaling in Myc heterozygotes suggests the presence of feedback loops within this regulatory network. In this communication we provide further evidence that the reduction of Myc expression in Myc+/− heterozygous mice provokes a female-specific decrease in circulating IGF1 as well as a reduction of IGF1 protein in the liver. In particular, reduced Myc expression led to upregulation of miRNAs that target the Igf1 transcript, thereby inhibiting its translation and leading to decreased IGF1 protein levels. Using Argonaute (AGO)-CLIP-sequencing we found enrichment of AGO binding in the Igf1 transcript at the target sites of let-7, miR-122, and miR-29 in female, but not male Myc heterozygotes. Upregulation of the liver-specific miR-122 in primary hepatocytes in culture and in vivo in mice resulted in significant downregulation of IGF1 protein, but not mRNA. Reduced levels of IGF1 increased GH production in the pituitary through a well-documented negative-feedback relationship. In line with this, we found that IGF1 levels in bone (where miR-122 is not expressed) were unchanged, consistent with the decreased incidence of osteoporosis in female Myc heterozygotes, despite decreased circulating IGF1.https://www.frontiersin.org/articles/10.3389/fcell.2023.1269860/fullMYC proto-oncogenemiRNA regulationIGF1 signalingsomatotrophic axisgender effectsosteoporosis
spellingShingle Anna P. Petrashen
Andrew D. Verdesca
Jill A. Kreiling
John M. Sedivy
Regulation of the somatotropic axis by MYC-mediated miRNA repression
Frontiers in Cell and Developmental Biology
MYC proto-oncogene
miRNA regulation
IGF1 signaling
somatotrophic axis
gender effects
osteoporosis
title Regulation of the somatotropic axis by MYC-mediated miRNA repression
title_full Regulation of the somatotropic axis by MYC-mediated miRNA repression
title_fullStr Regulation of the somatotropic axis by MYC-mediated miRNA repression
title_full_unstemmed Regulation of the somatotropic axis by MYC-mediated miRNA repression
title_short Regulation of the somatotropic axis by MYC-mediated miRNA repression
title_sort regulation of the somatotropic axis by myc mediated mirna repression
topic MYC proto-oncogene
miRNA regulation
IGF1 signaling
somatotrophic axis
gender effects
osteoporosis
url https://www.frontiersin.org/articles/10.3389/fcell.2023.1269860/full
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AT johnmsedivy regulationofthesomatotropicaxisbymycmediatedmirnarepression