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Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa

Friedman, James S.; Ray, Joseph W.; Waseem, Naushin; Johnson, Kory; Brooks, Matthew J.; Hugosson, Therése LU ; Breuer, Debra; Branham, Kari E.; Krauth, Daniel S. and Bowne, Sara J., et al. (2009) In American Journal of Human Genetics 84(6). p.792-800
Abstract
Retinitis pigmentosa (RP) refers to a genetically heterogeneous group of progressive neurodegenerative diseases that result in dysfunction and/or death of rod and cone photoreceptors in the retina. So far, 18 genes have been identified for autosomal-dominant (ad) RP. Here, we describe an adRP locus (RP42) at chromosome 7p15 through linkage analysis in a six-generation Scandinavian family and identify a disease-causing mutation, c.449G -> A (p.S150N), in exon 6 of the KLHL7 gene. Mutation screening of KLHL7 in 502 retinopathy probands has revealed three different missense mutations in six independent families. KLHL7 is widely expressed, including expression in rod photoreceptors, and encodes a 75 kDa protein of the BTB-Kelch Subfamily... (More)
Retinitis pigmentosa (RP) refers to a genetically heterogeneous group of progressive neurodegenerative diseases that result in dysfunction and/or death of rod and cone photoreceptors in the retina. So far, 18 genes have been identified for autosomal-dominant (ad) RP. Here, we describe an adRP locus (RP42) at chromosome 7p15 through linkage analysis in a six-generation Scandinavian family and identify a disease-causing mutation, c.449G -> A (p.S150N), in exon 6 of the KLHL7 gene. Mutation screening of KLHL7 in 502 retinopathy probands has revealed three different missense mutations in six independent families. KLHL7 is widely expressed, including expression in rod photoreceptors, and encodes a 75 kDa protein of the BTB-Kelch Subfamily within the BTB superfamily. BTB-Kelch proteins have been implicated in ubiquitination through Cullin E3 ligases. Notably, all three putative disease-causing KLHL7 mutations are within a conserved BACK domain; homology modeling suggests that mutant amino acid side chains can potentially fill the cleft between two helices, thereby affecting the ubiquitination complexes. Mutations in an identical region of another BTB-Kelch protein, gigaxonin, have previously been associated with giant axonal neuropathy. Our studies suggest an additional role of the ubiquitin-proteasome protein-degradation pathway in maintaining neuronal health and in disease. (Less)
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American Journal of Human Genetics
volume
84
issue
6
pages
792 - 800
publisher
Cell Press
external identifiers
  • wos:000267042800009
  • scopus:66449117927
ISSN
0002-9297
DOI
10.1016/j.ajhg.2009.05.007
language
English
LU publication?
yes
id
2dff2d11-9702-4fc9-b6ff-d0e165f19d8a (old id 1441781)
date added to LUP
2009-07-27 15:09:53
date last changed
2017-12-17 03:25:08
@article{2dff2d11-9702-4fc9-b6ff-d0e165f19d8a,
  abstract     = {Retinitis pigmentosa (RP) refers to a genetically heterogeneous group of progressive neurodegenerative diseases that result in dysfunction and/or death of rod and cone photoreceptors in the retina. So far, 18 genes have been identified for autosomal-dominant (ad) RP. Here, we describe an adRP locus (RP42) at chromosome 7p15 through linkage analysis in a six-generation Scandinavian family and identify a disease-causing mutation, c.449G -> A (p.S150N), in exon 6 of the KLHL7 gene. Mutation screening of KLHL7 in 502 retinopathy probands has revealed three different missense mutations in six independent families. KLHL7 is widely expressed, including expression in rod photoreceptors, and encodes a 75 kDa protein of the BTB-Kelch Subfamily within the BTB superfamily. BTB-Kelch proteins have been implicated in ubiquitination through Cullin E3 ligases. Notably, all three putative disease-causing KLHL7 mutations are within a conserved BACK domain; homology modeling suggests that mutant amino acid side chains can potentially fill the cleft between two helices, thereby affecting the ubiquitination complexes. Mutations in an identical region of another BTB-Kelch protein, gigaxonin, have previously been associated with giant axonal neuropathy. Our studies suggest an additional role of the ubiquitin-proteasome protein-degradation pathway in maintaining neuronal health and in disease.},
  author       = {Friedman, James S. and Ray, Joseph W. and Waseem, Naushin and Johnson, Kory and Brooks, Matthew J. and Hugosson, Therése and Breuer, Debra and Branham, Kari E. and Krauth, Daniel S. and Bowne, Sara J. and Sullivan, Lori S. and Ponjavic, Vesna and Gränse, Lotta and Khanna, Ritu and Trager, Edward H. and Gieser, Linn M. and Hughbanks-Wheaton, Dianna and Cojocaru, Radu I. and Ghiasvand, Noor M. and Chakarova, Christina F. and Abrahamson, Magnus and Goering, Harald H. H. and Webster, Andrew R. and Birch, David G. and Abecasis, Goncalo R. and Fann, Yang and Bhattacharya, Shomi S. and Daiger, Stephen P. and Heckenlively, John R. and Andréasson, Sten and Swaroop, Anand},
  issn         = {0002-9297},
  language     = {eng},
  number       = {6},
  pages        = {792--800},
  publisher    = {Cell Press},
  series       = {American Journal of Human Genetics},
  title        = {Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa},
  url          = {http://dx.doi.org/10.1016/j.ajhg.2009.05.007},
  volume       = {84},
  year         = {2009},
}