Please use this identifier to cite or link to this item:
https://www.arca.fiocruz.br/handle/icict/12447
COMPLEX GENOMIC REARRANGEMENTS AT THE PLP1 LOCUS INCLUDE TRIPLICATION AND QUADRUPLICATION
Haplotypes
Southern blot
Human genomics
Cloning
Genomic libraries
Genotyping
X chromosomes
Author
Affilliation
Baylor College of Medicine. Department of Molecular and Human Genetics. Houston, TX, United States of America
Baylor College of Medicine. Department of Molecular and Human Genetics. Houston, TX, United States of America/Fundação Oswaldo Cruz. Centro de Pesquisa Rene Rachou. Belo Horizonte, MG, Brasil
Alfred I. duPont Hospital for Children. Nemours Biomedical Research. Wilmington, DE, United States of America
Baylor College of Medicine. Department of Molecular and Human Genetics. Houston, TX, United States of America
Alfred I. duPont Hospital for Children. Nemours Biomedical Research. Wilmington, DE, United States of America
Baylor College of Medicine. Department of Molecular and Human Genetics. Houston, TX, United States of America
Alfred I. duPont Hospital for Children. Nemours Biomedical Research. Wilmington, DE, United States of America
Alfred I. duPont Hospital for Children. Nemours Biomedical Research. Wilmington, DE, United States of America/Thomas Jefferson University. Jefferson Medical College. Philadelphia, PA, United States of America
Georg August University. University Medical Center Göttingen. Division of Pediatric Neurology. Department of Pediatrics and Adolescent Medicine. Göttingen, Germany
Charles University and Motol University Hospital. 2nd Faculty of Medicine. Department of Pediatric Neurology. DNA Laboratory. Prague, Czech Republic
University of Rochester Medical Center. Rochester, NY, United States of America
Alfred I. duPont Hospital for Children. Nemours Biomedical Research. Wilmington, DE, United States of America/Thomas Jefferson University. Jefferson Medical College. Philadelphia, PA, United States of America/University of Delaware.Department of Biological Sciences. Newark, DA, United States of America
Baylor College of Medicine. Department of Molecular and Human Genetics. Houston, TX, United States of America/Baylor College of Medicine. Department of Pediatrics and Human Genome Sequencing Center. Houston, TX, United States of America/Texas Children ’s Hospital, Houston. TX, United States of America
Baylor College of Medicine. Department of Molecular and Human Genetics. Houston, TX, United States of America/Fundação Oswaldo Cruz. Centro de Pesquisa Rene Rachou. Belo Horizonte, MG, Brasil
Alfred I. duPont Hospital for Children. Nemours Biomedical Research. Wilmington, DE, United States of America
Baylor College of Medicine. Department of Molecular and Human Genetics. Houston, TX, United States of America
Alfred I. duPont Hospital for Children. Nemours Biomedical Research. Wilmington, DE, United States of America
Baylor College of Medicine. Department of Molecular and Human Genetics. Houston, TX, United States of America
Alfred I. duPont Hospital for Children. Nemours Biomedical Research. Wilmington, DE, United States of America
Alfred I. duPont Hospital for Children. Nemours Biomedical Research. Wilmington, DE, United States of America/Thomas Jefferson University. Jefferson Medical College. Philadelphia, PA, United States of America
Georg August University. University Medical Center Göttingen. Division of Pediatric Neurology. Department of Pediatrics and Adolescent Medicine. Göttingen, Germany
Charles University and Motol University Hospital. 2nd Faculty of Medicine. Department of Pediatric Neurology. DNA Laboratory. Prague, Czech Republic
University of Rochester Medical Center. Rochester, NY, United States of America
Alfred I. duPont Hospital for Children. Nemours Biomedical Research. Wilmington, DE, United States of America/Thomas Jefferson University. Jefferson Medical College. Philadelphia, PA, United States of America/University of Delaware.Department of Biological Sciences. Newark, DA, United States of America
Baylor College of Medicine. Department of Molecular and Human Genetics. Houston, TX, United States of America/Baylor College of Medicine. Department of Pediatrics and Human Genome Sequencing Center. Houston, TX, United States of America/Texas Children ’s Hospital, Houston. TX, United States of America
Abstract
Inverted repeats (IRs) can facilitate structural variation as crucibles of genomic rearrangement. Complex duplication—inverted triplication—duplication (DUP-TRP/INV-DUP) rearrangements that contain breakpoint junctions within IRs have been recently associated with both MECP2 duplication syndrome (MIM#300260) and Pelizaeus-Merzbacher disease (PMD, MIM#312080). We investigated 17 unrelated PMD subjects with copy number gains at the PLP1 locus including triplication and quadruplication of specific genomic intervals—16/17 were found to have a DUP-TRP/INV-DUP rearrangement product. An IR distal to PLP1 facilitates DUP-TRP/INV-DUP formation as well as an inversion structural variation found frequently amongst normal individuals. We show that a homology—or homeology—driven replicative mechanism of DNA repair can apparently mediate template switches within stretches of microhomology. Moreover, we provide evidence that quadruplication and potentially higher order amplification of a genomic interval can occur in a manner consistent with rolling circle amplification as predicted by the microhomology-mediated break induced replication (MMBIR)
Keywords
Polymerase chain reactionHaplotypes
Southern blot
Human genomics
Cloning
Genomic libraries
Genotyping
X chromosomes
Share