Article thumbnail

Mouse brain expression patterns of Spg7, Afg3l1, and Afg3l2 transcripts, encoding for the mitochondrial m-AAA protease

By Tiziana Sacco, Enrica Boda, Eriola Hoxha, Riccardo Pizzo, Claudia Cagnoli, Alfredo Brusco and Filippo Tempia
Topics: Research article
Publisher: BioMed Central
OAI identifier: oai:pubmedcentral.nih.gov:2880309
Provided by: PubMed Central

To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.

Suggested articles

Citations

  1. Akiyama Y: Cellular functions, mechanism of action, and regulation of FtsH protease.
  2. (1998). Ballabio A: Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease. Cell
  3. (2009). Casari G: Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degeneration.
  4. (2008). Casari G: The mitochondrial protease AFG3L2 is essential for axonal development.
  5. (2000). Greenamyre JT: Immunocytochemical characterization of the mitochondrially encoded ND1 subunit of complex I (NADH: ubiquinone oxidoreductase) in rat brain.
  6. (2000). Hereditary spastic paraparesis: a review of new developments.
  7. (2001). KBJ: The Mouse Brain in Stereotaxic Coordinates
  8. (2006). PB: Developmental time course of potassium channel expression in the rat cochlear nucleus. Hearing Research
  9. (2004). Rugarli EI: Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport.
  10. (2009). Rugarli EI: Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration. Hum Mol Genet
  11. (2009). Schüler H: Crystal structure of the ATPase domain of the human AAA+ protein paraplegin/SPG7. PLoS One
  12. (2005). T: The mAAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria. Cell
  13. (2010). Taroni F: Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. Nat Genet
  14. (2008). Taroni F: Spinocerebellar ataxia type 28: A novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis. Cerebellum
  15. (2009). Tempia F: Selection of reference genes for quantitative real time RT-PCR studies in mouse brain.
  16. (1998). The formation of respiratory chain complexes in mitochondria is under the proteolytic control of the m-AAA protease.
  17. (1996). The YTA10-12 complex, an AAA protease with chaperone-like activity in the inner membrane of mitochondria. Cell
  18. (2007). Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia. Mol Cell Biol