Refined localisation of the genes for nebulin and titin on chromosome 2q allows the assignment of nebulin as a candidate gene for autosomal recessive nemaline myopathy

被引:29
作者
Pelin, K
Ridanpaa, M
Donner, K
Wilton, S
Krishnarajah, J
Laing, N
Kolmerer, B
Millevoi, S
Labeit, S
delaChapelle, A
WallgrenPetterson, C
机构
[1] UNIV HELSINKI,DEPT MED GENET,HELSINKI,FINLAND
[2] FOLKHALSAN INST GENET,HELSINKI,FINLAND
[3] UNIV WESTERN AUSTRALIA,AUSTRALIAN NEUROMUSCULAR RES INST,NEDLANDS,WA 6009,AUSTRALIA
[4] EUROPEAN MOL BIOL LAB,HEIDELBERG,GERMANY
关键词
nebulin; titin; radiation hybrids; nemaline myopathy; rod myopathy; congenital myopathy;
D O I
10.1159/000484768
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
A locus for autosomal recessive nemaline myopathy (NEM2) has been assigned by linkage analysis to a 13-cM region between the markers D2S150 and D2S142 on 2q21.2-q22. The genes for the giant muscle proteins nebulin and titin have previously been assigned by FISH to 2q24.1-q24.2 and 2q31, respectively. By using radiation hybrid mapping, we have reassigned the nebulin gene close to the microsatellite marker D2S2236 on 2q22 and the titin gene to the vicinity of the markers D2S384 and D2S364 on 2q24.3. The genomic orientation of the nebulin gene was determined as 5'-3' and of TTN as 3'-5' from the centromere, We conclude that the nebulin gene resides within the candidate region for NEM2 on the long arm of chromosome 2, while the titin gene is located outside this region.
引用
收藏
页码:229 / 234
页数:6
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