4.6 Article

Gadd45a Protein Promotes Skeletal Muscle Atrophy by Forming a Complex with the Protein Kinase MEKK4

期刊

JOURNAL OF BIOLOGICAL CHEMISTRY
卷 291, 期 34, 页码 17496-17509

出版社

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M116.740308

关键词

aging; mass spectrometry (MS); muscle; muscle atrophy; skeletal muscle; skeletal muscle metabolism; Gadd45a; MEKK4

资金

  1. National Institutes of Health [R01AR059115, R01EY022616]
  2. United States Department of Veterans Affairs Biomedical Laboratory Research and Development Service Grant [IBX000976A]
  3. United States Department of Veterans Affairs Rehabilitation and Research Development Service Grant [1I01RX001477]
  4. Fraternal Order of Eagles Diabetes Research Center at the University of Iowa
  5. National Institutes of Health Shared Instrumentation Grant [1S10 OD016281]

向作者/读者索取更多资源

Skeletal muscle atrophy is a serious and highly prevalent condition that remains poorly understood at the molecular level. Previous work found that skeletal muscle atrophy involves an increase in skeletal muscle Gadd45a expression, which is necessary and sufficient for skeletal muscle fiber atrophy. However, the direct mechanism by which Gadd45a promotes skeletal muscle atrophy was unknown. To address this question, we biochemically isolated skeletal muscle proteins that associate with Gadd45a as it induces atrophy in mouse skeletal muscle fibers in vivo. We found that Gadd45a interacts with multiple proteins in skeletal muscle fibers, including, most prominently, MEKK4, a mitogen-activated protein kinase kinase kinase that was not previously known to play a role in skeletal muscle atrophy. Furthermore, we found that, by forming a complex with MEKK4 in skeletal muscle fibers, Gadd45a increases MEKK4 protein kinase activity, which is both sufficient to induce skeletal muscle fiber atrophy and required for Gadd45a-mediated skeletal muscle fiber atrophy. Together, these results identify a direct biochemical mechanism by which Gadd45a induces skeletal muscle atrophy and provide new insight into the way that skeletal muscle atrophy occurs at the molecular level.

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