Diminished OPA1 expression and impaired mitochondrial morphology and homeostasis in Aprataxin-deficient cells

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Diminished OPA1 expression and impaired mitochondrial morphology and homeostasis in Aprataxin-deficient cells. / Zheng, Jin; Croteau, Deborah L; Bohr, Vilhelm; Akbari, Mansour.

In: Nucleic Acids Research, Vol. 47, No. 8, 2019, p. 4086–4110.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Zheng, J, Croteau, DL, Bohr, V & Akbari, M 2019, 'Diminished OPA1 expression and impaired mitochondrial morphology and homeostasis in Aprataxin-deficient cells', Nucleic Acids Research, vol. 47, no. 8, pp. 4086–4110. https://doi.org/10.1093/nar/gkz083

APA

Zheng, J., Croteau, D. L., Bohr, V., & Akbari, M. (2019). Diminished OPA1 expression and impaired mitochondrial morphology and homeostasis in Aprataxin-deficient cells. Nucleic Acids Research, 47(8), 4086–4110. https://doi.org/10.1093/nar/gkz083

Vancouver

Zheng J, Croteau DL, Bohr V, Akbari M. Diminished OPA1 expression and impaired mitochondrial morphology and homeostasis in Aprataxin-deficient cells. Nucleic Acids Research. 2019;47(8):4086–4110. https://doi.org/10.1093/nar/gkz083

Author

Zheng, Jin ; Croteau, Deborah L ; Bohr, Vilhelm ; Akbari, Mansour. / Diminished OPA1 expression and impaired mitochondrial morphology and homeostasis in Aprataxin-deficient cells. In: Nucleic Acids Research. 2019 ; Vol. 47, No. 8. pp. 4086–4110.

Bibtex

@article{ea46b78ef9454145b8f8bfb87117c8f0,
title = "Diminished OPA1 expression and impaired mitochondrial morphology and homeostasis in Aprataxin-deficient cells",
abstract = "Ataxia with oculomotor apraxia type 1 (AOA1) is an early onset progressive spinocerebellar ataxia caused by mutation in aprataxin (APTX). APTX removes 5′-AMP groups from DNA, a product of abortive ligation during DNA repair and replication. APTX deficiency has been suggested to compromise mitochondrial function; however, a detailed characterization of mitochondrial homeostasis in APTX-deficient cells is not available. Here, we show that cells lacking APTX undergo mitochondrial stress and display significant changes in the expression of the mitochondrial inner membrane fusion protein optic atrophy type 1, and components of the oxidative phosphorylation complexes. At the cellular level, APTX deficiency impairs mitochondrial morphology and network formation, and autophagic removal of damaged mitochondria by mitophagy. Thus, our results show that aberrant mitochondrial function is a key component of AOA1 pathology. This work corroborates the emerging evidence that impaired mitochondrial function is a characteristic of an increasing number of genetically diverse neurodegenerative disorders.",
author = "Jin Zheng and Croteau, {Deborah L} and Vilhelm Bohr and Mansour Akbari",
year = "2019",
doi = "10.1093/nar/gkz083",
language = "English",
volume = "47",
pages = "4086–4110",
journal = "Nucleic Acids Research",
issn = "0305-1048",
publisher = "Oxford University Press",
number = "8",

}

RIS

TY - JOUR

T1 - Diminished OPA1 expression and impaired mitochondrial morphology and homeostasis in Aprataxin-deficient cells

AU - Zheng, Jin

AU - Croteau, Deborah L

AU - Bohr, Vilhelm

AU - Akbari, Mansour

PY - 2019

Y1 - 2019

N2 - Ataxia with oculomotor apraxia type 1 (AOA1) is an early onset progressive spinocerebellar ataxia caused by mutation in aprataxin (APTX). APTX removes 5′-AMP groups from DNA, a product of abortive ligation during DNA repair and replication. APTX deficiency has been suggested to compromise mitochondrial function; however, a detailed characterization of mitochondrial homeostasis in APTX-deficient cells is not available. Here, we show that cells lacking APTX undergo mitochondrial stress and display significant changes in the expression of the mitochondrial inner membrane fusion protein optic atrophy type 1, and components of the oxidative phosphorylation complexes. At the cellular level, APTX deficiency impairs mitochondrial morphology and network formation, and autophagic removal of damaged mitochondria by mitophagy. Thus, our results show that aberrant mitochondrial function is a key component of AOA1 pathology. This work corroborates the emerging evidence that impaired mitochondrial function is a characteristic of an increasing number of genetically diverse neurodegenerative disorders.

AB - Ataxia with oculomotor apraxia type 1 (AOA1) is an early onset progressive spinocerebellar ataxia caused by mutation in aprataxin (APTX). APTX removes 5′-AMP groups from DNA, a product of abortive ligation during DNA repair and replication. APTX deficiency has been suggested to compromise mitochondrial function; however, a detailed characterization of mitochondrial homeostasis in APTX-deficient cells is not available. Here, we show that cells lacking APTX undergo mitochondrial stress and display significant changes in the expression of the mitochondrial inner membrane fusion protein optic atrophy type 1, and components of the oxidative phosphorylation complexes. At the cellular level, APTX deficiency impairs mitochondrial morphology and network formation, and autophagic removal of damaged mitochondria by mitophagy. Thus, our results show that aberrant mitochondrial function is a key component of AOA1 pathology. This work corroborates the emerging evidence that impaired mitochondrial function is a characteristic of an increasing number of genetically diverse neurodegenerative disorders.

U2 - 10.1093/nar/gkz083

DO - 10.1093/nar/gkz083

M3 - Journal article

C2 - 30986824

VL - 47

SP - 4086

EP - 4110

JO - Nucleic Acids Research

JF - Nucleic Acids Research

SN - 0305-1048

IS - 8

ER -

ID: 213361665