The overall goal of this project is to define the mechanisms that are used to generate diverse muscle fiber types. In animals, different muscle fiber types arise to fine-tune the functions of individuals muscles, to enable those muscles to carry out their distinct roles in the animal. However, there is still much to learn of the cellular and molecular mechanisms that direct groups of myoblasts towards one fiber fate versus others. We have demonstrated that the flight muscles of the adult Drosophila thorax are specified and differentiate using mechanisms that are conserved with vertebrate fast fiber specification. Moreover, we have identified a number of transcriptional regulators that are required for formation of the flight muscles or of the physiologically-distinct jump muscles. In this renewal, we will build upon our studies to define conserved signaling and transcriptional pathways that give rise to different adult muscle fiber types. In the first aim, we will determine how ectodermal signals such as Wingless specify flight muscle specification via Vestigial and the flight muscle identity factor Spalt-major. In the second aim, we will define the roles of orthologs of mammalian Mohawk and Sox6 in regulating muscle fiber identity. In the third aim, we will focus upon how Vestigial and its cofactor Scalloped regulate jump muscle differentiation. Overall, our studies will provide significant new insight into how different muscle fiber types are generated during development in Drosophila. Importantly, our published and preliminary data provide significant evidence that conserved mechanisms regulate muscle fiber fate choices, indicating that our findings can be used as a valuable framework for understanding vertebrate muscle specification. Moreover, since muscle diseases and diabetes often affect the prevalence of one muscle fiber type over another, understanding the normal mechanisms of muscle fiber specification and maintenance can provide insight into the diseased state and how those conditions might be ameliorated.

Public Health Relevance

to public health: Understanding the transcriptional programs that control muscle fiber specification is a major area of investigation in muscle biology. Moreover, a number of human muscle diseases preferentially affect one class of muscles over another. By defining mechanisms for how individual muscles arise in the body, our studies will provide a deeper understanding of how some muscles might be more sensitive to the development of pathologies, and how the symptoms of such diseases might be ameliorated. !

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM061738-18
Application #
9661294
Study Section
Skeletal Muscle and Exercise Physiology Study Section (SMEP)
Program Officer
Hoodbhoy, Tanya
Project Start
2001-05-01
Project End
2023-02-28
Budget Start
2019-03-15
Budget End
2020-02-29
Support Year
18
Fiscal Year
2019
Total Cost
Indirect Cost
Name
San Diego State University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
073371346
City
San Diego
State
CA
Country
United States
Zip Code
92182
Dohn, Tracy E; Cripps, Richard M (2018) Absence of the Drosophila jump muscle actin Act79B is compensated by up-regulation of Act88F. Dev Dyn 247:642-649
Chechenova, Maria B; Maes, Sara; Oas, Sandy T et al. (2017) Functional redundancy and nonredundancy between two Troponin C isoforms in Drosophila adult muscles. Mol Biol Cell 28:760-770
Lovato, TyAnna L; Cripps, Richard M (2017) High Heart: A Role for Calcineurin Signaling in Hypoxia-Influenced Cardiac Growth. Circ Cardiovasc Genet 10:
Adema, Coen M; Hillier, LaDeana W; Jones, Catherine S et al. (2017) Whole genome analysis of a schistosomiasis-transmitting freshwater snail. Nat Commun 8:15451
Lovato, TyAnna L; Cripps, Richard M (2016) Regulatory Networks that Direct the Development of Specialized Cell Types in the Drosophila Heart. J Cardiovasc Dev Dis 3:
Chechenova, Maria B; Maes, Sara; Cripps, Richard M (2015) Expression of the Troponin C at 41C Gene in Adult Drosophila Tubular Muscles Depends upon Both Positive and Negative Regulatory Inputs. PLoS One 10:e0144615
Elwell, Jennifer A; Lovato, TyAnna L; Adams, Melanie M et al. (2015) The myogenic repressor gene Holes in muscles is a direct transcriptional target of Twist and Tinman in the Drosophila embryonic mesoderm. Dev Biol 400:266-76
Lovato, TyAnna L; Sensibaugh, Cheryl A; Swingle, Kirstie L et al. (2015) The Drosophila Transcription Factors Tinman and Pannier Activate and Collaborate with Myocyte Enhancer Factor-2 to Promote Heart Cell Fate. PLoS One 10:e0132965
Brunetti, Tonya M; Fremin, Brayon J; Cripps, Richard M (2015) Identification of singles bar as a direct transcriptional target of Drosophila Myocyte enhancer factor-2 and a regulator of adult myoblast fusion. Dev Biol 401:299-309
Oas, Sandy T; Bryantsev, Anton L; Cripps, Richard M (2014) Arrest is a regulator of fiber-specific alternative splicing in the indirect flight muscles of Drosophila. J Cell Biol 206:895-908

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