(Stroke. 2000;31:1935.)
© 2000 American Heart Association, Inc.
Original Contributions |
From the Department of Neurology (C.G.-G., C.T.-F., R.W., F.W., T.B.) and the Department of Dermatology (I.W., I.H.), University of Heidelberg, Heidelberg, Germany.
Correspondence to Dr C. Grond-Ginsbach, Department of Neurology, University of Heidelberg, Im Neuenheimer Feld 400, D-69120 Heidelberg, Germany. E-mail Caspar Grond-Ginsbach{at}med.uni-heidelberg.de
Background and PurposeThe majority of patients with spontaneous cerebral artery dissection show ultrastructural alterations in dermal collagen and elastic fibers.
MethodsWe studied the gene encoding tropoelastin (ELN) by reverse transcriptionpolymerase chain reaction and subsequent sequence analysis in 10 patients with abnormalities in their elastic fibers.
ResultsNo mutations were found in the whole coding region of the ELN gene. The simultaneous visualization and quantification of ELN splice variants by gene scanning enabled the analysis of the regulation of alternative splicing of ELN mRNA. No differences could be detected between fibroblast cultures of the patients and a control subject.
ConclusionsNeither mutations in the ELN gene nor dysregulation of its activity appears to be the cause of the connective tissue disorder that is found in most patients with spontaneous dissections.
Key Words: dissections RNA splicing, alternative sequence analysis tropoelastin
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