A cDNA clone from the Duchenne/Becker muscular dystrophy gene (original) (raw)
- Letter
- Published: 30 July 1987
- Cairine Logan1,
- Xiuyuan Hu1,
- Bonnie Belfall1,
- Ronald G. Worton1 &
- …
- Peter N. Ray1
Nature volume 328, pages 434–437 (1987)Cite this article
- 382 Accesses
- 242 Citations
- 6 Altmetric
- Metrics details
Abstract
Duchenne muscular dystrophy (DMD) is the most common of the muscular dystrophies affecting one in 3,000 live male births (see refs 1, 2 for review). Both DMD and the mild form, Becker muscular dystrophy (BMD), are X-linked. There are a number of females affected by the disease who all possess an X-autosome translocation, with the exchange point in the X always occurring within chromosome band Xp21 (refs 3, 4). This, together with linkage and deletion data, has localized the gene at band Xp21 (refs 5–7). DNA fragments from this region have been cloned using a patient with a large Xp21 deletion8 and from a patient with a t(X:21) translocation9. The former clones (pERT87) comprise the DXS164 locus and the latter clones (XJ) the DXS206 locus. Subclones from both regions allow the detection of deletions in ∼11% of DMD patients8–12. A fetal muscle complementary DNA clone corresponding to exons in the DXS164 locus has been isolated and detects a 16-kilobase (kb) transcript13. We present the isolation of an adult muscle cDNA clone from the DXS206 locus that detects a 16-kb mRNA in adult human muscle. The cDNA clone contains exons that map in the DXS206 locus, the DXS164 locus, and on the centromeric side of these cloned regions. The t(X;21) translocation exchange points occurs within a large intron of 105 kb or larger, indicating that the translocation has disrupted the DMD/BMD gene to cause the disease in this patient.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Additional access options:
Similar content being viewed by others
Author information
Authors and Affiliations
- Genetics Department and Research Institute, The Hospital for Sick Children and The Departments of Medical Genetics and Biophysics, University of Toronto, 555 University Avenue, Toronto, Ontario, M5G 1X8, Canada
Arthur H. M. Burghes, Cairine Logan, Xiuyuan Hu, Bonnie Belfall, Ronald G. Worton & Peter N. Ray
Authors
- Arthur H. M. Burghes
You can also search for this author inPubMed Google Scholar - Cairine Logan
You can also search for this author inPubMed Google Scholar - Xiuyuan Hu
You can also search for this author inPubMed Google Scholar - Bonnie Belfall
You can also search for this author inPubMed Google Scholar - Ronald G. Worton
You can also search for this author inPubMed Google Scholar - Peter N. Ray
You can also search for this author inPubMed Google Scholar
Rights and permissions
About this article
Cite this article
Burghes, A., Logan, C., Hu, X. et al. A cDNA clone from the Duchenne/Becker muscular dystrophy gene.Nature 328, 434–437 (1987). https://doi.org/10.1038/328434a0
- Received: 05 May 1987
- Accepted: 26 June 1987
- Issue Date: 30 July 1987
- DOI: https://doi.org/10.1038/328434a0