2016
DOI: 10.1038/nature21034
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mTORC1 and muscle regeneration are regulated by the LINC00961-encoded SPAR polypeptide

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Cited by 496 publications
(397 citation statements)
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“…These animals manifest no apparent developmental abnormalities, but their skeletal muscle shows enhanced regeneration capacity after acute injury as well as enhanced mTORC1 activation. These observations are consistent with the abundance of Spar mRNA in skeletal muscle of wild-type mice as well as with the fact that amino acid-induced mTORC1 activation is required for regeneration after muscle injury, and they suggest that mTORC1 activation is precisely regulated by the SPAR polypeptide in a tissue-specific manner (Matsumoto et al, 2017).…”
Section: (5) Sparsupporting
confidence: 75%
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“…These animals manifest no apparent developmental abnormalities, but their skeletal muscle shows enhanced regeneration capacity after acute injury as well as enhanced mTORC1 activation. These observations are consistent with the abundance of Spar mRNA in skeletal muscle of wild-type mice as well as with the fact that amino acid-induced mTORC1 activation is required for regeneration after muscle injury, and they suggest that mTORC1 activation is precisely regulated by the SPAR polypeptide in a tissue-specific manner (Matsumoto et al, 2017).…”
Section: (5) Sparsupporting
confidence: 75%
“…Of note, SPAR had no obvious effect on lysosomal acidification but was found to inhibit mTORC1 activation by amino acids through regulation of the v-ATPase-Ragulator supercomplex (Fig. 3E) (Matsumoto et al, 2017).…”
Section: (5) Sparmentioning
confidence: 99%
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“…This regulatory network has now been extended by the work of Matsumoto et al who demonstrate that SPAR, a polypeptide translated from lncRNA LINC00961, inhibits amino acid-mediated mTORC1 activation at the lysosomal membrane [7]. SPAR was discovered by proteomics aimed at identifying polypeptides encoded by lncRNAs.…”
mentioning
confidence: 99%