Literature DB >> 8394647

Nuclear complementation restores mtDNA levels in cultured cells from a patient with mtDNA depletion.

A G Bodnar1, J M Cooper, I J Holt, J V Leonard, A H Schapira.   

Abstract

We have studied cultured skin fibroblasts from a patient with a fatal mitochondrial disease manifesting soon after birth. These fibroblasts were found to grow only in the presence of pyruvate and uridine, a characteristic of cells lacking mtDNA (rho0 cells). Southern blot and PCR analyses confirmed that the patient's fibroblasts contained less than 2% of control levels of mtDNA. Biochemical analyses indicated that the activities of all the respiratory-chain enzymes were severely decreased in mitochondria isolated from these fibroblasts. In order to elucidate the underlying molecular defect, cell fusions were performed between enucleated fibroblasts from this patient and a human-derived rho0 cell line (rho0 A549.B2). The resulting cybrids were plated in medium lacking pyruvate and uridine, to select for the restoration of respiratory-chain function. Complementation was observed between the nuclear genome of the rho0 A549.B2 cells and the mtDNA of the patient's cells, restoring mtDNA levels and respiratory-chain function in the cybrid cells. These results indicate that mtDNA depletion in our patient is under the control of the nuclear genome.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8394647      PMCID: PMC1682435     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  19 in total

1.  Mitochondrial phosphoenolpyruvate carboxykinase deficiency.

Authors:  J V Leonard; K Hyland; N Furukawa; P T Clayton
Journal:  Eur J Pediatr       Date:  1991-01       Impact factor: 3.183

2.  Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation.

Authors:  M P King; G Attardi
Journal:  Science       Date:  1989-10-27       Impact factor: 47.728

3.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

4.  A rapid protocol for the purification of mitochondrial DNA suitable for studying restriction fragment length polymorphisms.

Authors:  C Welter; S Dooley; N Blin
Journal:  Gene       Date:  1989-11-15       Impact factor: 3.688

5.  Mitochondrial phosphoenolpyruvate carboxykinase deficiency.

Authors:  P T Clayton; K Hyland; M Brand; J V Leonard
Journal:  Eur J Pediatr       Date:  1986-04       Impact factor: 3.183

6.  Rapid isolation of animal mitochondrial DNA by alkaline extraction.

Authors:  T K Palva; E T Palva
Journal:  FEBS Lett       Date:  1985-11-18       Impact factor: 4.124

7.  An established avian fibroblast cell line without mitochondrial DNA.

Authors:  P Desjardins; J M de Muys; R Morais
Journal:  Somat Cell Mol Genet       Date:  1986-03

Review 8.  Replication of animal mitochondrial DNA.

Authors:  D A Clayton
Journal:  Cell       Date:  1982-04       Impact factor: 41.582

9.  Regulation of adipose tissue pyruvate dehydrogenase by insulin and other hormones.

Authors:  H G Coore; R M Denton; B R Martin; P J Randle
Journal:  Biochem J       Date:  1971-11       Impact factor: 3.857

10.  mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases.

Authors:  C T Moraes; S Shanske; H J Tritschler; J R Aprille; F Andreetta; E Bonilla; E A Schon; S DiMauro
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

View more
  19 in total

1.  Mitochondrial DNA depletion syndrome is expressed in amniotic fluid cell cultures.

Authors:  J C Blake; J W Taanman; A M Morris; R G Gray; J M Cooper; P J McKiernan; J V Leonard; A H Schapira
Journal:  Am J Pathol       Date:  1999-07       Impact factor: 4.307

2.  Prohibitins act as a membrane-bound chaperone for the stabilization of mitochondrial proteins.

Authors:  L G Nijtmans; L de Jong; M Artal Sanz; P J Coates; J A Berden; J W Back; A O Muijsers; H van der Spek; L A Grivell
Journal:  EMBO J       Date:  2000-06-01       Impact factor: 11.598

3.  Mitochondrial transfer between cells can rescue aerobic respiration.

Authors:  Jeffrey L Spees; Scott D Olson; Mandolin J Whitney; Darwin J Prockop
Journal:  Proc Natl Acad Sci U S A       Date:  2006-01-23       Impact factor: 11.205

Review 4.  Disorders of gluconeogenesis.

Authors:  G van den Berghe
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

5.  Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts.

Authors:  V Procaccio; B Mousson; R Beugnot; H Duborjal; F Feillet; G Putet; I Pignot-Paintrand; A Lombès; R De Coo; H Smeets; J Lunardi; J P Issartel
Journal:  J Clin Invest       Date:  1999-07       Impact factor: 14.808

6.  Diagnostic value of succinate ubiquinone reductase activity in the identification of patients with mitochondrial DNA depletion.

Authors:  P Hargreaves; S Rahman; P Guthrie; J W Taanman; J V Leonard; J M Land; S J R Heales
Journal:  J Inherit Metab Dis       Date:  2002-02       Impact factor: 4.982

7.  Apparent functional independence of the mitochondrial and nuclear transcription systems in cultured human cells.

Authors:  R Sewards; B Wiseman; H T Jacobs
Journal:  Mol Gen Genet       Date:  1994-12-15

8.  Early-onset fatal encephalomyopathy associated with severe mtDNA depletion.

Authors:  V Paquis-Flucklinger; J F Pellissier; J Camboulives; B Chabrol; A Saunières; M F Monfort; H Giudicelli; C Desnuelle
Journal:  Eur J Pediatr       Date:  1995-07       Impact factor: 3.183

9.  Altered gene transcription profiles in fibroblasts harboring either TK2 or DGUOK mutations indicate compensatory mechanisms.

Authors:  Joan Villarroya; Carme de Bolós; Anna Meseguer; Michio Hirano; Maya R Vilà
Journal:  Exp Cell Res       Date:  2009-03-03       Impact factor: 3.905

10.  Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain.

Authors:  A A Morris; R W Taylor; M A Birch-Machin; M J Jackson; M G Coulthard; L A Bindoff; R J Welch; N Howell; D M Turnbull
Journal:  Pediatr Nephrol       Date:  1995-08       Impact factor: 3.714

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.