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PMID: 11968085 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Characterization of breakpoint sequences of five rearrangements in L1CAM and ABCD1 (ALD) genes.

Human mutation ·Vol. 19 ·No. 5 ·2002-05-00 ·Pages 526-35

Kutsche K, Ressler B, Katzera HG, Orth U, Gillessen-Kaesbach G, Morlot S, Schwinger E, Gal A

Abstract

Mutations in L1CAM are responsible for X-linked hydrocephalus, whereas those in the ALD gene (ABCD1) cause adrenoleukodystrophy. In both genes, most of the mutations reported so far are short-length mutations and only a few patients with larger rearrangements have been documented. We have characterized three intragenic deletions of the ALD gene at the molecular level and describe here the first two L1CAM rearrangements resulting in deletion of several exons in one case and about 50 kb, including the entire gene, in the second case. At both breakpoints of an ALD deletion, Alu repeats have been found and, additionally, a short Alu region of approximately 130 bp was inserted, suggesting that this rearrangement is the result of a more complex non-allelic homologous recombination event. Only one Alu element was present at the breakpoint of the second ALD rearrangement, including a 26-bp Alu core sequence that was suggested to be a recombinogenic hot spot. These data suggest the involvement of an Alu core sequence-stimulated non-homologous recombination as a possible cause for this rearrangement. Short direct repeats were identified at all putative mispaired sequences in the L1CAM breakpoints and at both breakpoints of the third ALD deletion characterized, suggesting non-homologous (illegitimate) recombination as the molecular mechanism by which these latter deletions occurred. In conclusion, our results indicate that highly repetitive elements as well as short direct repeats are frequently involved in the formation of ALD and L1CAM gene rearrangements.

MeSH Terms
ATP Binding Cassette Transporter, Subfamily D, Member 1 ATP-Binding Cassette Transporters/genetics Adrenoleukodystrophy/genetics Alu Elements/genetics Antigens, Surface/genetics Base Sequence Chemokine CCL22 Chemokines, CC Chromosome Breakage/genetics Chromosome Deletion Female Gene Rearrangement/genetics Genetic Linkage/genetics Humans Infant Leukocyte L1 Antigen Complex Male Membrane Glycoproteins/genetics Membrane Proteins/genetics Molecular Sequence Data Neural Cell Adhesion Molecules/genetics Recombination, Genetic/genetics X Chromosome/genetics
Chemicals
ABCD1 protein, human ATP Binding Cassette Transporter, Subfamily D, Member 1 ATP-Binding Cassette Transporters Antigens, Surface CCL22 protein, human Chemokine CCL22 Chemokines, CC Leukocyte L1 Antigen Complex Membrane Glycoproteins Membrane Proteins Neural Cell Adhesion Molecules
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Kutsche Kerstin
Institut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany. kkutsche@uke.uni-hamburg.de
Ressler Bernadette
Katzera Heide-Gertrude
Orth Ulrike
Gillessen-Kaesbach Gabriele
Morlot Susanne
Schwinger Eberhard
Gal Andreas
Article Info
Journal
Human mutation
Abbr.
Hum Mutat
ISSN
1098-1004
Published
2002-05-00
Pages
526-35
Language
English
Region
United States
NLM ID
9215429
Subset
IM
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