Matches in SemOpenAlex for { <https://semopenalex.org/work/W4284693836> ?p ?o ?g. }
- W4284693836 endingPage "267" @default.
- W4284693836 startingPage "260" @default.
- W4284693836 abstract "Biallelic pathogenic variants in the nuclear gene DARS2 (MIM# 610956), encoding the mitochondrial enzyme aspartyl-tRNA synthetase (MT-ASPRS) cause leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Lactate Elevation (LBSL) (MIM# 611105), a neurometabolic disorder characterized by progressive ataxia, spasticity, developmental arrest or regression and characteristic brain MRI findings. Most patients exhibit a slowly progressive disease course with motor deterirartion that begins in childhood or adolescence, but can also occasionaly occur in adulthood. More severe LBSL presentations with atypical brain MRI findings have been recently described. Baker's yeast orthologue of DARS2, MSD1, is required for growth on oxidative carbon sources. A yeast with MSD1 knockout (msd1Δ) demonstrated a complete lack of oxidative growth which could be rescued by wild-type MSD1 but not MSD1 with pathogenic variants. Here we reported two siblings who exhibited developmental regression and ataxia with different age of onset and phenotypic severity. Exome sequencing revealed 2 compound heterozygous missense variants in DARS2: c.473A>T (p.Glu158Val) and c.829G>A (p.Glu277Lys); this variant combination has not been previously reported. The msd1Δ yeast transformed with plasmids expressing p.Glu259Lys, equivalent to human p.Glu277Lys, showed complete loss of oxidative growth and oxygen consumption, while the strain carrying p.Gln137Val, equivalent to human p.Glu158Val, showed a significant reduction of oxidative growth, but a residual ability to grow was retained. Structural analysis indicated that p.Glu158Val may interfere with protein binding of tRNAAsp, while p.Glu277Lys may impact both homodimerization and catalysis of MT-ASPRS. Our data illustrate the utility of yeast model and in silico analysis to determine pathogenicity of DARS2 variants, expand the genotypic spectrum and suggest intrafamilial variability in LBSL." @default.
- W4284693836 created "2022-07-08" @default.
- W4284693836 creator A5005087345 @default.
- W4284693836 creator A5034827238 @default.
- W4284693836 creator A5049020514 @default.
- W4284693836 creator A5057295149 @default.
- W4284693836 creator A5057794593 @default.
- W4284693836 creator A5059281499 @default.
- W4284693836 creator A5076294242 @default.
- W4284693836 creator A5079340502 @default.
- W4284693836 creator A5080016627 @default.
- W4284693836 date "2022-08-01" @default.
- W4284693836 modified "2023-10-17" @default.
- W4284693836 title "Functional analysis of missense DARS2 variants in siblings with leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation" @default.
- W4284693836 cites W1511041944 @default.
- W4284693836 cites W1970413157 @default.
- W4284693836 cites W1978742484 @default.
- W4284693836 cites W2004807060 @default.
- W4284693836 cites W2012849860 @default.
- W4284693836 cites W2022665563 @default.
- W4284693836 cites W2051575430 @default.
- W4284693836 cites W2051978340 @default.
- W4284693836 cites W2059319775 @default.
- W4284693836 cites W2073505231 @default.
- W4284693836 cites W2100780019 @default.
- W4284693836 cites W2195303995 @default.
- W4284693836 cites W2521967673 @default.
- W4284693836 cites W2605462664 @default.
- W4284693836 cites W2743084346 @default.
- W4284693836 cites W2751686252 @default.
- W4284693836 cites W2897434952 @default.
- W4284693836 cites W2905452503 @default.
- W4284693836 cites W2982914835 @default.
- W4284693836 cites W3029661147 @default.
- W4284693836 cites W3084025367 @default.
- W4284693836 cites W3128482208 @default.
- W4284693836 cites W3129566372 @default.
- W4284693836 cites W3158540459 @default.
- W4284693836 cites W3175071069 @default.
- W4284693836 cites W3180963866 @default.
- W4284693836 cites W3199639770 @default.
- W4284693836 cites W4221017463 @default.
- W4284693836 doi "https://doi.org/10.1016/j.ymgme.2022.07.002" @default.
- W4284693836 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35820270" @default.
- W4284693836 hasPublicationYear "2022" @default.
- W4284693836 type Work @default.
- W4284693836 citedByCount "1" @default.
- W4284693836 countsByYear W42846938362022 @default.
- W4284693836 crossrefType "journal-article" @default.
- W4284693836 hasAuthorship W4284693836A5005087345 @default.
- W4284693836 hasAuthorship W4284693836A5034827238 @default.
- W4284693836 hasAuthorship W4284693836A5049020514 @default.
- W4284693836 hasAuthorship W4284693836A5057295149 @default.
- W4284693836 hasAuthorship W4284693836A5057794593 @default.
- W4284693836 hasAuthorship W4284693836A5059281499 @default.
- W4284693836 hasAuthorship W4284693836A5076294242 @default.
- W4284693836 hasAuthorship W4284693836A5079340502 @default.
- W4284693836 hasAuthorship W4284693836A5080016627 @default.
- W4284693836 hasBestOaLocation W42846938361 @default.
- W4284693836 hasConcept C104317684 @default.
- W4284693836 hasConcept C12125453 @default.
- W4284693836 hasConcept C126322002 @default.
- W4284693836 hasConcept C127716648 @default.
- W4284693836 hasConcept C134018914 @default.
- W4284693836 hasConcept C16671776 @default.
- W4284693836 hasConcept C169760540 @default.
- W4284693836 hasConcept C2776151105 @default.
- W4284693836 hasConcept C2778583010 @default.
- W4284693836 hasConcept C2779134260 @default.
- W4284693836 hasConcept C2780906641 @default.
- W4284693836 hasConcept C54355233 @default.
- W4284693836 hasConcept C71924100 @default.
- W4284693836 hasConcept C75563809 @default.
- W4284693836 hasConcept C86803240 @default.
- W4284693836 hasConceptScore W4284693836C104317684 @default.
- W4284693836 hasConceptScore W4284693836C12125453 @default.
- W4284693836 hasConceptScore W4284693836C126322002 @default.
- W4284693836 hasConceptScore W4284693836C127716648 @default.
- W4284693836 hasConceptScore W4284693836C134018914 @default.
- W4284693836 hasConceptScore W4284693836C16671776 @default.
- W4284693836 hasConceptScore W4284693836C169760540 @default.
- W4284693836 hasConceptScore W4284693836C2776151105 @default.
- W4284693836 hasConceptScore W4284693836C2778583010 @default.
- W4284693836 hasConceptScore W4284693836C2779134260 @default.
- W4284693836 hasConceptScore W4284693836C2780906641 @default.
- W4284693836 hasConceptScore W4284693836C54355233 @default.
- W4284693836 hasConceptScore W4284693836C71924100 @default.
- W4284693836 hasConceptScore W4284693836C75563809 @default.
- W4284693836 hasConceptScore W4284693836C86803240 @default.
- W4284693836 hasFunder F4320310094 @default.
- W4284693836 hasFunder F4320332591 @default.
- W4284693836 hasFunder F4320337611 @default.
- W4284693836 hasIssue "4" @default.
- W4284693836 hasLocation W42846938361 @default.
- W4284693836 hasLocation W42846938362 @default.
- W4284693836 hasOpenAccess W4284693836 @default.
- W4284693836 hasPrimaryLocation W42846938361 @default.
- W4284693836 hasRelatedWork W1799753142 @default.