Journal article
Akirin Is Required for Muscle Function and Acts Through the TGF-β Sma/Mab Signaling Pathway in Caenorhabditis elegans Development
G3 (Bethesda, Md.), Vol.10(1), pp.387-400
01/07/2020
DOI: 10.1534/g3.119.400377
PMCID: PMC6945016
PMID: 31767636
Abstract
Akirin, a conserved metazoan protein, functions in muscle development in flies and mice. However, this was only tested in the rodent and fly model systems. Akirin was shown to act with chromatin remodeling complexes in transcription and was established as a downstream target of the NFκB pathway. Here we show a role for
Akirin/AKIR-1 in the muscle and body length regulation through a different pathway. Akirin localizes to somatic tissues throughout the body of
, including muscle nuclei. In agreement with its role in other model systems, Akirin loss of function mutants exhibit defects in muscle development in the embryo, as well as defects in movement and maintenance of muscle integrity in the
adult. We also have determined that Akirin acts downstream of the TGF-β Sma/Mab signaling pathway in controlling body size. Moreover, we found that the loss of Akirin resulted in an increase in autophagy markers, similar to mutants in the TGF-β Sma/Mab signaling pathway. In contrast to what is known in rodent and fly models,
Akirin does not act with the SWI/SNF chromatin-remodeling complex, and is instead involved with the NuRD chromatin remodeling complex in both movement and regulation of body size. Our studies define a novel developmental role (body size) and a new pathway (TGF-β Sma/Mab) for Akirin function, and confirmed its evolutionarily conserved function in muscle development in a new organism.
Details
- Title: Subtitle
- Akirin Is Required for Muscle Function and Acts Through the TGF-β Sma/Mab Signaling Pathway in Caenorhabditis elegans Development
- Creators
- Richard Bowman - Department of Biology University of Iowa, Iowa City, IA 52240 andNathan Balukoff - Department of Biology University of Iowa, Iowa City, IA 52240 andAmy Clemons - Department of Biology University of Iowa, Iowa City, IA 52240 andEmily Koury - Department of Biology University of Iowa, Iowa City, IA 52240 andTalitha Ford - Department of Biology University of Iowa, Iowa City, IA 52240 andKunal Baxi - Department of Biology, University of Saskatchewan, 112 Science Place, Saskatoon, SK, S7N 5E2Carlos Egydio de Carvalho - Department of Biology, University of Saskatchewan, 112 Science Place, Saskatoon, SK, S7N 5E2Sarit Smolikove - Department of Biology University of Iowa, Iowa City, IA 52240 and sarit-smolikove@uiowa.edu
- Resource Type
- Journal article
- Publication Details
- G3 (Bethesda, Md.), Vol.10(1), pp.387-400
- DOI
- 10.1534/g3.119.400377
- PMID
- 31767636
- PMCID
- PMC6945016
- NLM abbreviation
- G3 (Bethesda)
- ISSN
- 2160-1836
- eISSN
- 2160-1836
- Grant note
- P40 OD010440 / NIH HHS
- Language
- English
- Date published
- 01/07/2020
- Academic Unit
- Biology
- Record Identifier
- 9984217421202771
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