Periaxin mutations cause recessive Dejerine-Sottas neuropathy

被引:158
作者
Boerkoel, CF
Takashima, H
Stankiewicz, P
Garcia, CA
Leber, SM
Rhee-Morris, L
Lupski, JR
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
[3] Tulane Univ, Dept Neurol, New Orleans, LA 70118 USA
[4] Tulane Univ, Dept Pathol, New Orleans, LA 70118 USA
[5] Univ Michigan, Med Ctr, Div Pediat Neurol, Ann Arbor, MI USA
[6] Univ Calif Davis Hlth Syst, Dept Obstet & Gynecol, Prenatal Diag & Treatment Ctr, Sacramento, CA USA
关键词
D O I
10.1086/318208
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The periaxin gene (PRX) encodes two PDZ-domain proteins, L- and S-periaxin, that are required for maintenance of peripheral nerve myelin. Prx(-/-) mice develop a severe demyelinating peripheral neuropathy, despite apparently normal initial formation of myelin sheaths. We hypothesized that mutations in PRX could cause human peripheral myelinopathies. In accordance with this, we identified three unrelated Dejerine-Sottas neuropathy patients with recessive PRX mutations-two with compound heterozygous nonsense and frameshift mutations, and one with a homozygous frameshift mutation. We mapped PRX to 19q13.13-13.2, a region recently associated with a severe autosomal recessive demyelinating neuropathy in a Lebanese family (Delague et al. 2000) and syntenic to the location of Prx on murine chromosome 7 (Gillespie et al. 1997).
引用
收藏
页码:325 / 333
页数:9
相关论文
共 28 条
[1]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[2]   Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family:: Exclusion of MAG as a candidate gene [J].
Delague, V ;
Bareil, C ;
Tuffery, S ;
Bouvagnet, P ;
Chouery, E ;
Koussa, S ;
Maisonobe, T ;
Loiselet, J ;
Mégarbané, A ;
Claustres, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (01) :236-243
[3]  
den Dunnen JT, 2000, HUM MUTAT, V15, P7
[4]   Two PDZ domain proteins encoded by the murine periaxin gene are the result of alternative intron retention and are differentially targeted in Schwann cells [J].
Dytrych, L ;
Sherman, DL ;
Gillespie, CS ;
Brophy, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (10) :5794-5800
[5]   Protein modules as organizers of membrane structure [J].
Fanning, AS ;
Anderson, JM .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (04) :432-439
[6]   Actin plays a role in both changes in cell shape and gene-expression associated with Schwann cell myelination [J].
FernandezValle, C ;
Gorman, D ;
Gomez, AM ;
Bunge, MB .
JOURNAL OF NEUROSCIENCE, 1997, 17 (01) :241-250
[7]   Peripheral demyelination and neuropathic pain behavior in periaxin-deficient mice [J].
Gillespie, CS ;
Sherman, DL ;
Fleetwood-Walker, SM ;
Cottrell, DF ;
Tait, S ;
Garry, EM ;
Wallace, VCJ ;
Ure, J ;
Griffiths, IR ;
Smith, A ;
Brophy, PJ .
NEURON, 2000, 26 (02) :523-531
[8]   PERIAXIN, A NOVEL PROTEIN OF MYELINATING SCHWANN-CELLS WITH A POSSIBLE ROLE IN AXONAL ENSHEATHMENT [J].
GILLESPIE, CS ;
SHERMAN, DL ;
BLAIR, GE ;
BROPHY, PJ .
NEURON, 1994, 12 (03) :497-508
[9]   The gene encoding the Schwann cell protein periaxin localizes on mouse chromosome 7 (Prx) [J].
Gillespie, CS ;
Lee, M ;
Fantes, JF ;
Brophy, PJ .
GENOMICS, 1997, 41 (02) :297-298
[10]   DE-NOVO MUTATION OF THE MYELIN P(O) GENE IN DEJERINE-SOTTAS DISEASE (HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-III) [J].
HAYASAKA, K ;
HIMORO, M ;
SAWAISHI, Y ;
NANAO, K ;
TAKAHASHI, T ;
TAKADA, G ;
NICHOLSON, GA ;
OUVRIER, RA ;
TACHI, N .
NATURE GENETICS, 1993, 5 (03) :266-268