Christopher M Adams1, Scott M Ebert, Michael C Dyle. 1. aDepartment of Internal Medicine bDepartment of Molecular Physiology and Biophysics cFraternal Order of Eagles Diabetes Research Center, Roy J. and Lucille A. Carver College of Medicine, The University of Iowa dIowa City Veterans Affairs Medical Center, Iowa City eEmmyon, Inc., Coralville, Iowa, USA.
Abstract
PURPOSE OF REVIEW: Here, we discuss recent work focused on the role of activating transcription factor 4 (ATF4) in skeletal muscle atrophy. RECENT FINDINGS: Muscle atrophy involves and requires widespread changes in skeletal muscle gene expression; however, the transcriptional regulatory proteins responsible for those changes are not yet well defined. Recent work indicates that some forms of muscle atrophy require ATF4, a stress-inducible bZIP transcription factor subunit that helps to mediate a broad range of stress responses in mammalian cells. ATF4 expression in skeletal muscle fibers is sufficient to induce muscle fiber atrophy and required for muscle atrophy during several stress conditions, including aging, fasting, and limb immobilization. By helping to activate specific genes in muscle fibers, ATF4 contributes to the expression of numerous mRNAs, including at least two mRNAs (Gadd45a and p21) that encode mediators of muscle fiber atrophy. Gadd45a promotes muscle fiber atrophy by activating the protein kinase MEKK4. p21 promotes atrophy by reducing expression of spermine oxidase, a metabolic enzyme that helps to maintain muscle fiber size under nonstressed conditions. SUMMARY: In skeletal muscle fibers, ATF4 is critical component of a complex and incompletely understood molecular signaling network that causes muscle atrophy during aging, fasting, and immobilization.
PURPOSE OF REVIEW: Here, we discuss recent work focused on the role of activating transcription factor 4 (ATF4) in skeletal muscle atrophy. RECENT FINDINGS:Muscle atrophy involves and requires widespread changes in skeletal muscle gene expression; however, the transcriptional regulatory proteins responsible for those changes are not yet well defined. Recent work indicates that some forms of muscle atrophy require ATF4, a stress-inducible bZIP transcription factor subunit that helps to mediate a broad range of stress responses in mammalian cells. ATF4 expression in skeletal muscle fibers is sufficient to induce muscle fiber atrophy and required for muscle atrophy during several stress conditions, including aging, fasting, and limb immobilization. By helping to activate specific genes in muscle fibers, ATF4 contributes to the expression of numerous mRNAs, including at least two mRNAs (Gadd45a and p21) that encode mediators of muscle fiber atrophy. Gadd45a promotes muscle fiber atrophy by activating the protein kinase MEKK4. p21 promotes atrophy by reducing expression of spermine oxidase, a metabolic enzyme that helps to maintain muscle fiber size under nonstressed conditions. SUMMARY: In skeletal muscle fibers, ATF4 is critical component of a complex and incompletely understood molecular signaling network that causes muscle atrophy during aging, fasting, and immobilization.
Authors: Michael Munroe; Svyatoslav Dvoretskiy; Amber Lopez; Jiayu Leong; Michael C Dyle; Hyunjoon Kong; Christopher M Adams; Marni D Boppart Journal: FASEB J Date: 2019-04-25 Impact factor: 5.191
Authors: Daniel J Ham; Anastasiya Börsch; Shuo Lin; Marco Thürkauf; Martin Weihrauch; Judith R Reinhard; Julien Delezie; Fabienne Battilana; Xueyong Wang; Marco S Kaiser; Maitea Guridi; Michael Sinnreich; Mark M Rich; Nitish Mittal; Lionel A Tintignac; Christoph Handschin; Mihaela Zavolan; Markus A Rüegg Journal: Nat Commun Date: 2020-09-09 Impact factor: 14.919
Authors: Gavin Pharaoh; Jacob L Brown; Kavithalakshmi Sataranatarajan; Parker Kneis; Jan Bian; Rojina Ranjit; Niran Hadad; Constantin Georgescu; Peter Rabinovitch; Qitao Ran; Jonathan D Wren; Willard Freeman; Michael Kinter; Arlan Richardson; Holly Van Remmen Journal: Sci Rep Date: 2020-08-18 Impact factor: 4.996