SwePub
Sök i LIBRIS databas

  Extended search

WFRF:(Lochmuller H.)
 

Search: WFRF:(Lochmuller H.) > Metabolic shift und...

Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency

Hathazi, D. (author)
Griffin, H. (author)
Jennings, M. J. (author)
show more...
Giunta, M. (author)
Powell, C. (author)
Pearce, S. F. (author)
Munro, B. (author)
Wei, W. (author)
Boczonadi, V. (author)
Poulton, J. (author)
Pyle, A. (author)
Calabrese, C. (author)
Gomez-Duran, A. (author)
Schara, U. (author)
Pitceathly, R. D. (author)
Hanna, M. G. (author)
Joost, K. (author)
Cotta, A. (author)
Paim, J. F. (author)
Navarro, M. M. (author)
Duff, J. (author)
Mattmann, A. (author)
Chapman, K. (author)
Servidei, S. (author)
Della Marina, A. (author)
Uusimaa, J. (author)
Roos, A. (author)
Mootha, V. (author)
Hirano, M. (author)
Tulinius, Mar, 1953 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics
Giri, M. (author)
Hoffmann, E. P. (author)
Lochmuller, H. (author)
DiMauro, S. (author)
Minczuk, M. (author)
Chinnery, P. F. (author)
Muller, J. S. (author)
Horvath, R. (author)
show less...
 (creator_code:org_t)
2020-10-31
2020
English.
In: Embo Journal. - : EMBO. - 0261-4189 .- 1460-2075. ; 39:23
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Reversible infantile respiratory chain deficiency (RIRCD) is a rare mitochondrial myopathy leading to severe metabolic disturbances in infants, which recover spontaneously after 6-months of age. RIRCD is associated with the homoplasmic m.14674T>C mitochondrial DNA mutation; however, only similar to 1/100 carriers develop the disease. We studied 27 affected and 15 unaffected individuals from 19 families and found additional heterozygous mutations in nuclear genes interacting with mt-tRNAGlu including EARS2 and TRMU in the majority of affected individuals, but not in healthy carriers of m.14674T>C, supporting a digenic inheritance. Our transcriptomic and proteomic analysis of patient muscle suggests a stepwise mechanism where first, the integrated stress response associated with increased FGF21 and GDF15 expression enhances the metabolism modulated by serine biosynthesis, one carbon metabolism, TCA lipid oxidation and amino acid availability, while in the second step mTOR activation leads to increased mitochondrial biogenesis. Our data suggest that the spontaneous recovery in infants with digenic mutations may be modulated by the above described changes. Similar mechanisms may explain the variable penetrance and tissue specificity of other mtDNA mutations and highlight the potential role of amino acids in improving mitochondrial disease.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)

Keyword

digenic inheritance
homoplasmic tRNA mutation
mitochondrial myopathy
reversible infantile respiratory chain deficiency
citric-acid cycle
stress-response
mitochondrial translation
reaction-mechanism
fatty-acid
key role
rna
glutaminase
regulator
oxidation
Biochemistry & Molecular Biology
Cell Biology

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view