Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues

被引:53
作者
Filisetti, D
Ostermann, G
von Bredow, M
Strom, T
Filler, G
Ehrich, J
Pannetier, S
Garnier, JM
Rowe, P
Francis, F
Julienne, A
Hanauer, A
Econs, MJ
Oudet, C
机构
[1] ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, France
[2] Humboldt Univ, Fak Med, Univ Klinikum Charite, Univ Klin Kinderheilkunde,Abt Kindernephrol, D-1040 Berlin, Germany
[3] Univ Munich, Abt Med Genet, Kinderpoliklin, Munich, Germany
[4] Med Hsch Hannover, Dept Pediat Nephrol Orthoped Dent & Radiol, Hannover, Germany
[5] Univ London, Royal Free Hosp, Sch Med, Dept Biochem & Mol Biol, London WC1E 7HU, England
[6] CHU Cochin Port Royal, INSERM, U129, Inst Cochin Genet Mol, Paris, France
[7] Hop Lariboisiere, Ctr Viggo Petersen, INSERM, U349, F-75475 Paris, France
[8] Indiana Univ, Sch Med, Dept Med, Indianapolis, IN USA
关键词
X-linked hypophosphataemia; vitamin D resistant rickets; PHEX gene; endopeptidase; HYP phenotype; mutation distribution;
D O I
10.1038/sj.ejhg.5200341
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Thirty newly detected mutations in the PHEX gene are reported, and pooled with all the previously published mutations, The spectrum of mutations displayed 16% deletions, 8% insertions, 34% missense, 27% nonsense, and 15% splice site mutations, with two peaks in exon 15, and 17, Since 32.8% of PHEX amino acids were conserved in the endopeptidases family, the number of missense mutations detected at non-conserved residues was smaller than expected, whereas the number of nonsense mutations observed at non-conserved residues was very close to the expected number, Compared with conserved amino acids, the changes in nonconserved amino acids may result in benign polymorphisms or possibly mild disease that may go undiagnosed.
引用
收藏
页码:615 / 619
页数:5
相关论文
共 18 条
[1]   Pex/PEX tissue distribution and evidence for a deletion in the 3' region of the Pex gene in X-linked hypophosphatemic mice [J].
Beck, L ;
Soumounou, Y ;
Martel, J ;
Krishnamurthy, G ;
Gauthier, C ;
Goodyer, CG ;
Tenenhouse, HS .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (06) :1200-1209
[2]  
Berndt M, 1996, CLIN NEPHROL, V45, P33
[3]   New perspectives on the biology and treatment of X-linked hypophosphatemic rickets [J].
Carpenter, TO .
PEDIATRIC CLINICS OF NORTH AMERICA, 1997, 44 (02) :443-+
[4]   Mutational analysis of PHEX gene in X-linked hypophosphatemia [J].
Dixon, PH ;
Christie, PT ;
Wooding, C ;
Trump, D ;
Grieff, M ;
Holm, I ;
Gertner, JM ;
Schmidtke, J ;
Shah, B ;
Shaw, N ;
Smith, C ;
Tau, C ;
Schlessinger, D ;
Whyte, MP ;
Thakker, RV .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (10) :3615-3623
[5]   cDNA cloning of the murine Pex gene implicated in X-linked hypophosphatemia and evidence for expression in bone [J].
Du, L ;
Desbarats, M ;
Viel, J ;
Glorieux, FH ;
Cawthorn, C ;
Ecarot, B .
GENOMICS, 1996, 36 (01) :22-28
[6]   X-LINKED HYPOPHOSPHATEMIC RICKETS - A DISEASE OFTEN UNKNOWN TO AFFECTED PATIENTS [J].
ECONS, MJ ;
SAMSA, GP ;
MONGER, M ;
DREZNER, MK ;
FEUSSNER, JR .
BONE AND MINERAL, 1994, 24 (01) :17-24
[7]   Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets [J].
Francis, F ;
Strom, TM ;
Hennig, S ;
Boddrich, A ;
Lorenz, B ;
Brandau, O ;
Mohnike, KL ;
Cagnoli, M ;
Steffens, C ;
Klages, S ;
Borzym, K ;
Pohl, T ;
Oudet, C ;
Econs, MJ ;
Rowe, PSN ;
Reinhardt, R ;
Meitinger, T ;
Lehrach, H .
GENOME RESEARCH, 1997, 7 (06) :573-585
[8]   A GENE (PEX) WITH HOMOLOGIES TO ENDOPEPTIDASES IS MUTATED IN PATIENTS WITH X-LINKED HYPOPHOSPHATEMIC RICKETS [J].
FRANCIS, F ;
HENNIG, S ;
KORN, B ;
REINHARDT, R ;
DEJONG, P ;
POUSTKA, A ;
LEHRACH, H ;
ROWE, PSN ;
GOULDING, JN ;
SUMMERFIELD, T ;
MOUNTFORD, R ;
READ, AP ;
POPOWSKA, E ;
PRONICKA, E ;
DAVIES, KE ;
ORIORDAN, JLH ;
ECONS, MJ ;
NESBITT, T ;
DREZNER, MK ;
OUDET, C ;
PANNETIER, S ;
HANAUER, A ;
STROM, TM ;
MEINDL, A ;
LORENZ, B ;
CAGNOLI, M ;
MOHNIKE, KL ;
MURKEN, J ;
MEITINGER, T .
NATURE GENETICS, 1995, 11 (02) :130-136
[9]   Sequence analysis of 139 kb in Xp22.1 containing spermine synthase and the 5' region of PEX [J].
Grieff, M ;
Whyte, MP ;
Thakker, RV ;
Mazzarella, R .
GENOMICS, 1997, 44 (02) :227-231
[10]  
GUO R, 1997, AM SOC BONE MINERAL, V127, P1009