Literature DB >> 23223238

Gene knockout using transcription activator-like effector nucleases (TALENs) reveals that human NDUFA9 protein is essential for stabilizing the junction between membrane and matrix arms of complex I.

David A Stroud1, Luke E Formosa, Xiaonan W Wijeyeratne, Thanh N Nguyen, Michael T Ryan.   

Abstract

Transcription activator-like effector nucleases (TALENs) represent a promising approach for targeted knock-out of genes in cultured human cells. We used TALEN-technology to knock out the nuclear gene encoding NDUFA9, a subunit of mitochondrial respiratory chain complex I in HEK293T cells. Screening for the knock-out revealed a mixture of NDUFA9 cell clones that harbored partial deletions of the mitochondrial N-terminal targeting signal but were still capable of import. A cell line lacking functional copies of both NDUFA9 alleles resulted in a loss of NDUFA9 protein expression, impaired assembly of complex I, and cells incapable of growth in galactose medium. Cells lacking NDUFA9 contained a complex I subcomplex consisting of membrane arm subunits but not marker subunits of the matrix arm. Re-expression of NDUFA9 restored the defects in complex I assembly. We conclude that NDUFA9 is involved in stabilizing the junction between membrane and matrix arms of complex I, a late assembly step critical for complex I biogenesis and activity.

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Year:  2012        PMID: 23223238      PMCID: PMC3548478          DOI: 10.1074/jbc.C112.436766

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  32 in total

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4.  Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I.

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7.  Nonviability of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblasts.

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  33 in total

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2.  Effect of Aging on Mitochondrial Energetics in the Human Atria.

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6.  Exploring the quinone/inhibitor-binding pocket in mitochondrial respiratory complex I by chemical biology approaches.

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7.  Activation of TRPV1 attenuates high salt-induced cardiac hypertrophy through improvement of mitochondrial function.

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9.  Cooperative and independent roles of the Drp1 adaptors Mff, MiD49 and MiD51 in mitochondrial fission.

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10.  Optic atrophy-associated TMEM126A is an assembly factor for the ND4-module of mitochondrial complex I.

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