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

J Biol Chem. 2013 Jan 18;288(3):1685-90. doi: 10.1074/jbc.C112.436766. Epub 2012 Dec 5.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Deoxyribonucleases / metabolism*
  • Electron Transport Complex I / chemistry
  • Electron Transport Complex I / deficiency
  • Electron Transport Complex I / genetics
  • Electron Transport Complex I / metabolism*
  • Exons
  • Gene Expression
  • Gene Knockout Techniques
  • HEK293 Cells
  • Humans
  • Membrane Potential, Mitochondrial / genetics
  • Mitochondria / chemistry
  • Mitochondria / enzymology
  • Mitochondria / genetics*
  • Mitochondrial Membranes / chemistry*
  • Mitochondrial Membranes / enzymology
  • Molecular Sequence Data
  • Transcriptional Activation

Substances

  • Deoxyribonucleases
  • Electron Transport Complex I
  • NDUFA9 protein, human