Skip Navigation



Human Molecular Genetics Advance Access published online on February 2, 2005

Human Molecular Genetics, doi:10.1093/hmg/ddi073
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Supplementary Material
Right arrow All Versions of this Article:
14/6/785    most recent
ddi073v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Thatcher, K. N.
Right arrow Articles by LaSalle, J. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Thatcher, K. N.
Right arrow Articles by LaSalle, J. M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Molecular Genetics © Oxford University Press 2005; all rights reserved

Article

Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples

Karen N. Thatcher 1, Sailaja Peddada 1, Dag H. Yasui 1, and Janine M. LaSalle 2*

1 Medical Microbiology and Immunology and Rowe Program in Human Genetics, School of Medicine, University of California, Davis, CA
2 Medical Microbiology and Immunology and Rowe Program in Human Genetics, School of Medicine, University of California, One Shields Ave., Davis, CA 95616

* To whom correspondence should be addressed.
Janine M. LaSalle, E-mail: jmlasalle{at}ucdavis.edu


   Abstract

Rett syndrome (RTT), caused by mutations in MECP2 (encoding methyl CpG binding protein 2), and Angelman syndrome (AS), caused by maternal deficiency of chromosome 15q11-13, are autism-spectrum neurodevelopmental disorders. MeCP2 is a transcriptional repressor of methylated genes, but MECP2 mutation does not directly affect the imprinted expression of genes within 15q11-13. We tested a potential role for MeCP2 in the homologous pairing of imprinted 15q11-13 alleles in human brain tissue and differentiated neurons by fluorescence in situ hybridization (FISH). FISH analysis of control cerebral samples demonstrated a significant increase in homologous pairing specific to chromosome 15 from infant to juvenile brain samples. Significant and specific deficiencies in the percentage of paired chromosome 15 alleles were observed in RTT, AS, and autism brain samples compared to normal controls. SH-SY5Y neuroblastoma cells also showed a significant and specific increase in the percentage of chromosome 15q11-13 paired alleles following induced differentiation in vitro. Transfection with a methylated oligonucleotide decoy specifically blocked binding of MeCP2 to the SNURF/SNRPN promoter within 15q11-13 and significantly lowered the percentage of paired 15q11-13 alleles in SH-SY5Y cells. These combined results suggest a role for MeCP2 in chromosome organization in the developing brain and provide a potential mechanistic association between several related neurodevelopmental disorders.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Hum Mol GenetHome page
K. N. Leung, R. O. Vallero, A. J. DuBose, J. L. Resnick, and J. M. LaSalle
Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size
Hum. Mol. Genet., November 15, 2009; 18(22): 4227 - 4238.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
S. E. Swanberg, R. P. Nagarajan, S. Peddada, D. H. Yasui, and J. M. LaSalle
Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism
Hum. Mol. Genet., February 1, 2009; 18(3): 525 - 534.
[Abstract] [Full Text] [PDF]


Home page
J. Med. Genet.Home page
A Hogart, K N Leung, N J Wang, D J Wu, J Driscoll, R O Vallero, N C Schanen, and J M LaSalle
Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number
J. Med. Genet., February 1, 2009; 46(2): 86 - 93.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
A. Kumar, S. Kamboj, B. M. Malone, S. Kudo, J. L. Twiss, K. J. Czymmek, J. M. LaSalle, and N. C. Schanen
Analysis of protein domains and Rett syndrome mutations indicate that multiple regions influence chromatin-binding dynamics of the chromatin-associated protein MECP2 in vivo
J. Cell Sci., April 1, 2008; 121(7): 1128 - 1137.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
D. H. Yasui, S. Peddada, M. C. Bieda, R. O. Vallero, A. Hogart, R. P. Nagarajan, K. N. Thatcher, P. J. Farnham, and J. M. LaSalle
Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes
PNAS, December 4, 2007; 104(49): 19416 - 19421.
[Abstract] [Full Text] [PDF]


Home page
PediatricsHome page
C. P. Johnson, S. M. Myers, and and the Council on Children With Disabilities
Identification and Evaluation of Children With Autism Spectrum Disorders
Pediatrics, November 1, 2007; 120(5): 1183 - 1215.
[Abstract] [Full Text] [PDF]


Home page
JCBHome page
C. M. Caldwell, R. A. Green, and K. B. Kaplan
APC mutations lead to cytokinetic failures in vitro and tetraploid genotypes in Min mice
J. Cell Biol., September 24, 2007; 178(7): 1109 - 1120.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
B. R. Williams, J. R. Bateman, N. D. Novikov, and C.-T. Wu
Disruption of Topoisomerase II Perturbs Pairing in Drosophila Cell Culture
Genetics, September 1, 2007; 177(1): 31 - 46.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
A. Hogart, R. P. Nagarajan, K. A. Patzel, D. H. Yasui, and J. M. LaSalle
15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders
Hum. Mol. Genet., March 15, 2007; 16(6): 691 - 703.
[Abstract] [Full Text] [PDF]


Home page
AutismHome page
R. Delong
GABA(A) receptor alpha5 subunit as a candidate gene for autism and bipolar disorder: A proposed endophenotype with parent-of-origin and gain-of-function features,with or without oculocutaneous albinism
Autism, March 1, 2007; 11(2): 135 - 147.
[Abstract] [PDF]


Home page
GeneticsHome page
A. M. Lee and C.-t. Wu
Enhancer-Promoter Communication at the yellow Gene of Drosophila melanogaster: Diverse Promoters Participate in and Regulate trans Interactions
Genetics, December 1, 2006; 174(4): 1867 - 1880.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
S. Peddada, D. H. Yasui, and J. M. LaSalle
Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome
Hum. Mol. Genet., June 15, 2006; 15(12): 2003 - 2014.
[Abstract] [Full Text] [PDF]


Home page
CMAJHome page
D. Rodenhiser and M. Mann
Epigenetics and human disease: translating basic biology into clinical applications
Can. Med. Assoc. J., January 31, 2006; 174(3): 341 - 348.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.