Missense mutations in the BCS1L gene as a cause of the Björnstad syndrome.

Abstract

BACKGROUND:

The Björnstad syndrome, an autosomal recessive disorder associated with sensorineural hearing loss and pili torti, is caused by mutation of a previously unidentified gene on chromosome 2q34-36.

METHODS:

Refined genetic mapping and DNA sequencing of 44 genes between D2S2210 and D2S2244 revealed BCS1L mutations. Functional analyses elucidated how BCS1L mutations cause the Björnstad syndrome.

RESULTS:

BCS1L encodes a member of the AAA family of ATPases that is necessary for the assembly of complex III in the mitochondria. In addition to the Björnstad syndrome, BCS1L mutations cause complex III deficiency and the GRACILE syndrome, which in neonates are lethal conditions that have multisystem and neurologic manifestations typifying severe mitochondrial disorders. Patients with the Björnstad syndrome have mutations that alter residues involved in protein-protein interactions, whereas mutations in patients with complex III deficiency alter ATP-binding residues, as deduced from the crystal structure of a related AAA-family ATPase. Biochemical studies provided evidence to support this model: complex III deficiency mutations prevented ATP-dependent assembly of BCS1L-associated complexes. All mutant BCS1L proteins disrupted the assembly of complex III, reduced the activity of the mitochondrial electron-transport chain, and increased the production of reactive oxygen species. However, only mutations associated with complex III deficiency increased mitochondrial content, which further increased the production of reactive oxygen species.

CONCLUSIONS:

BCS1L mutations cause disease phenotypes ranging from highly restricted pili torti and sensorineural hearing loss (the Björnstad syndrome) to profound multisystem organ failure (complex III deficiency and the GRACILE syndrome). All BCS1L mutations disrupted the assembly of mitochondrial respirasomes (the basic unit for respiration in human mitochondria), but the clinical expression of the mutations was correlated with the production of reactive oxygen species. Mutations that cause the Björnstad syndrome illustrate the exquisite sensitivity of ear and hair tissues to mitochondrial function, particularly to the production of reactive oxygen species.

• Authors: J Travis Hinson, Valeria R Fantin, Jost Schönberger, Noralv Breivik, Geir Siem, Barbara McDonough, Pankaj Sharma, Ivan Keogh, Ricardo Godinho, Felipe Santos, Alfonso Esparza, Yamileth Nicolau, Edgar Selvaag, Bruce H Cohen, Charles L Hoppel, Lisbeth Tranebjaerg, Roland D Eavey, J G Seidman, Christine E Seidman
• Journal: The New England journal of medicine (N Engl J Med) Vol. 356 Issue 8 Pg. 809-19 (Feb 22 2007) ISSN: 1533-4406 [Electronic] United States
• PMID: 17314340 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
• Copyright: Copyright 2007 Massachusetts Medical Society.

Chemical References

• BCS1L protein, human
• Bacterial Proteins
• RuvB protein, Bacteria
• ATPases Associated with Diverse Cellular Activities
• Electron Transport Complex III

Topics

• ATPases Associated with Diverse Cellular Activities
• Bacterial Proteins (chemistry)
• Child, Preschool
• DNA Mutational Analysis
• Electron Transport Complex III (chemistry, genetics)
• Female
• Hair Diseases (genetics)
• Hearing Loss, Sensorineural (genetics)
• Humans
• Male
• Mitochondria
• Mutation, Missense
• Pedigree
• Protein Structure, Tertiary
• Sequence Homology, Amino Acid
• Syndrome
• Yeasts