Literature DB >> 9359044

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.

K Pelin1, M Ridanpää, K Donner, S Wilton, J Krishnarajah, N Laing, B Kolmerer, S Millevoi, S Labeit, A de la Chapelle, C Wallgren-Petterson.   

Abstract

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.

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Year:  1997        PMID: 9359044

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  5 in total

1.  Nemaline myopathy in the Ashkenazi Jewish population is caused by a deletion in the nebulin gene.

Authors:  Sylvia L Anderson; Josef Ekstein; Mary C Donnelly; Erin M Keefe; Nicole R Toto; Lauretta A LeVoci; Berish Y Rubin
Journal:  Hum Genet       Date:  2004-06-23       Impact factor: 4.132

Review 2.  Muscle giants: molecular scaffolds in sarcomerogenesis.

Authors:  Aikaterini Kontrogianni-Konstantopoulos; Maegen A Ackermann; Amber L Bowman; Solomon V Yap; Robert J Bloch
Journal:  Physiol Rev       Date:  2009-10       Impact factor: 37.312

3.  Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy.

Authors:  K Pelin; P Hilpelä; K Donner; C Sewry; P A Akkari; S D Wilton; D Wattanasirichaigoon; M L Bang; T Centner; F Hanefeld; S Odent; M Fardeau; J A Urtizberea; F Muntoni; V Dubowitz; A H Beggs; N G Laing; S Labeit; A de la Chapelle; C Wallgren-Pettersson
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

4.  Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2q.

Authors:  P Nicolao; F Xiang; L G Gunnarsson; B Giometto; L Edström; M Anvret; Z Zhang
Journal:  Am J Hum Genet       Date:  1999-03       Impact factor: 11.025

5.  Human skeletal myosin heavy chain genes are tightly linked in the order embryonic-IIa-IId/x-ILb-perinatal-extraocular.

Authors:  J B Shrager; P R Desjardins; J M Burkman; S K Konig; S K Stewart; L Su; M C Shah; E Bricklin; M Tewari; R Hoffman; M R Rickels; E H Jullian; N A Rubinstein; H H Stedman
Journal:  J Muscle Res Cell Motil       Date:  2000-05       Impact factor: 2.698

  5 in total

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