Molecular regulation of high muscle mass in developing Blonde d'Aquitaine cattle foetuses
Identifieur interne : 000786 ( Main/Exploration ); précédent : 000785; suivant : 000787Molecular regulation of high muscle mass in developing Blonde d'Aquitaine cattle foetuses
Auteurs : Isabelle Cassar-Malek [France] ; Céline Boby [France] ; Brigitte Picard [France] ; Antonio Reverter [Australie] ; Nicholas J. Hudson [Australie]Source :
- Biology Open [ 2046-6390 ] ; 2017.
Abstract
The Blonde d'Aquitaine (BA) is a French cattle breed with enhanced muscularity, partly attributable to a
Url:
DOI: 10.1242/bio.024950
PubMed: 28838967
PubMed Central: 5665461
Affiliations:
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Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Molecular regulation of high muscle mass in developing Blonde d'Aquitaine cattle foetuses</title>
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<author><name sortKey="Boby, Celine" sort="Boby, Celine" uniqKey="Boby C" first="Céline" last="Boby">Céline Boby</name>
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<series><title level="j">Biology Open</title>
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<front><div type="abstract" xml:lang="en"><title>ABSTRACT</title>
<p>The Blonde d'Aquitaine (BA) is a French cattle breed with enhanced muscularity, partly attributable to a <italic>MSTN</italic>
mutation. The BA <italic>m. Semitendinosus</italic>
has a faster muscle fibre isoform phenotype comprising a higher proportion of fast type IIX fibres compared to age-matched Charolais (CH). To better understand the molecular network of modifications in BA compared to CH muscle, we assayed the transcriptomes of the <italic>m. Semitendinosus</italic>
at 110, 180, 210 and 260 days postconception (dpc). We used a combination of differential expression (DE) and regulatory impact factors (RIF) to compare and contrast muscle gene expression between the breeds. Prominently developmentally regulated genes in both breeds reflected the replacement of embryonic myosin isoforms (<italic>MYL4</italic>
, <italic>MYH3</italic>
) with adult isoforms (<italic>MYH1</italic>
) and the upregulation of mitochondrial metabolism (<italic>CKMT2</italic>
, <italic>AGXT2L1</italic>
) in preparation for birth. However, the transition to a fast, glycolytic muscle phenotype in the MSTN mutant BA is detectable through downregulation of various slow twitch subunits (<italic>TNNC1</italic>
, <italic>MYH7</italic>
, <italic>TPM3</italic>
, <italic>CSRP3</italic>
) beyond 210 dpc, and a small but consistent genome-wide reduction in mRNA encoding the mitoproteome. Across the breeds, <italic>NRIP2</italic>
is the regulatory gene possessing a network change most similar to that of <italic>MSTN</italic>
.</p>
</div>
</front>
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</TEI>
<affiliations><list><country><li>Australie</li>
<li>France</li>
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<tree><country name="France"><noRegion><name sortKey="Cassar Malek, Isabelle" sort="Cassar Malek, Isabelle" uniqKey="Cassar Malek I" first="Isabelle" last="Cassar-Malek">Isabelle Cassar-Malek</name>
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