Cargando…

Smchd1-Dependent and -Independent Pathways Determine Developmental Dynamics of CpG Island Methylation on the Inactive X Chromosome

X chromosome inactivation involves multiple levels of chromatin modification, established progressively and in a stepwise manner during early development. The chromosomal protein Smchd1 was recently shown to play an important role in DNA methylation of CpG islands (CGIs), a late step in the X inacti...

Descripción completa

Detalles Bibliográficos
Autores principales: Gendrel, Anne-Valerie, Apedaile, Anwyn, Coker, Heather, Termanis, Ausma, Zvetkova, Ilona, Godwin, Jonathan, Tang, Y. Amy, Huntley, Derek, Montana, Giovanni, Taylor, Steven, Giannoulatou, Eleni, Heard, Edith, Stancheva, Irina, Brockdorff, Neil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437444/
https://www.ncbi.nlm.nih.gov/pubmed/22841499
http://dx.doi.org/10.1016/j.devcel.2012.06.011
_version_ 1782242786740797440
author Gendrel, Anne-Valerie
Apedaile, Anwyn
Coker, Heather
Termanis, Ausma
Zvetkova, Ilona
Godwin, Jonathan
Tang, Y. Amy
Huntley, Derek
Montana, Giovanni
Taylor, Steven
Giannoulatou, Eleni
Heard, Edith
Stancheva, Irina
Brockdorff, Neil
author_facet Gendrel, Anne-Valerie
Apedaile, Anwyn
Coker, Heather
Termanis, Ausma
Zvetkova, Ilona
Godwin, Jonathan
Tang, Y. Amy
Huntley, Derek
Montana, Giovanni
Taylor, Steven
Giannoulatou, Eleni
Heard, Edith
Stancheva, Irina
Brockdorff, Neil
author_sort Gendrel, Anne-Valerie
collection PubMed
description X chromosome inactivation involves multiple levels of chromatin modification, established progressively and in a stepwise manner during early development. The chromosomal protein Smchd1 was recently shown to play an important role in DNA methylation of CpG islands (CGIs), a late step in the X inactivation pathway that is required for long-term maintenance of gene silencing. Here we show that inactive X chromosome (Xi) CGI methylation can occur via either Smchd1-dependent or -independent pathways. Smchd1-dependent CGI methylation, the primary pathway, is acquired gradually over an extended period, whereas Smchd1-independent CGI methylation occurs rapidly after the onset of X inactivation. The de novo methyltransferase Dnmt3b is required for methylation of both classes of CGI, whereas Dnmt3a and Dnmt3L are dispensable. Xi CGIs methylated by these distinct pathways differ with respect to their sequence characteristics and immediate chromosomal environment. We discuss the implications of these results for understanding CGI methylation during development.
format Online
Article
Text
id pubmed-3437444
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Cell Press
record_format MEDLINE/PubMed
spelling pubmed-34374442012-09-12 Smchd1-Dependent and -Independent Pathways Determine Developmental Dynamics of CpG Island Methylation on the Inactive X Chromosome Gendrel, Anne-Valerie Apedaile, Anwyn Coker, Heather Termanis, Ausma Zvetkova, Ilona Godwin, Jonathan Tang, Y. Amy Huntley, Derek Montana, Giovanni Taylor, Steven Giannoulatou, Eleni Heard, Edith Stancheva, Irina Brockdorff, Neil Dev Cell Article X chromosome inactivation involves multiple levels of chromatin modification, established progressively and in a stepwise manner during early development. The chromosomal protein Smchd1 was recently shown to play an important role in DNA methylation of CpG islands (CGIs), a late step in the X inactivation pathway that is required for long-term maintenance of gene silencing. Here we show that inactive X chromosome (Xi) CGI methylation can occur via either Smchd1-dependent or -independent pathways. Smchd1-dependent CGI methylation, the primary pathway, is acquired gradually over an extended period, whereas Smchd1-independent CGI methylation occurs rapidly after the onset of X inactivation. The de novo methyltransferase Dnmt3b is required for methylation of both classes of CGI, whereas Dnmt3a and Dnmt3L are dispensable. Xi CGIs methylated by these distinct pathways differ with respect to their sequence characteristics and immediate chromosomal environment. We discuss the implications of these results for understanding CGI methylation during development. Cell Press 2012-08-14 /pmc/articles/PMC3437444/ /pubmed/22841499 http://dx.doi.org/10.1016/j.devcel.2012.06.011 Text en © 2012 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Gendrel, Anne-Valerie
Apedaile, Anwyn
Coker, Heather
Termanis, Ausma
Zvetkova, Ilona
Godwin, Jonathan
Tang, Y. Amy
Huntley, Derek
Montana, Giovanni
Taylor, Steven
Giannoulatou, Eleni
Heard, Edith
Stancheva, Irina
Brockdorff, Neil
Smchd1-Dependent and -Independent Pathways Determine Developmental Dynamics of CpG Island Methylation on the Inactive X Chromosome
title Smchd1-Dependent and -Independent Pathways Determine Developmental Dynamics of CpG Island Methylation on the Inactive X Chromosome
title_full Smchd1-Dependent and -Independent Pathways Determine Developmental Dynamics of CpG Island Methylation on the Inactive X Chromosome
title_fullStr Smchd1-Dependent and -Independent Pathways Determine Developmental Dynamics of CpG Island Methylation on the Inactive X Chromosome
title_full_unstemmed Smchd1-Dependent and -Independent Pathways Determine Developmental Dynamics of CpG Island Methylation on the Inactive X Chromosome
title_short Smchd1-Dependent and -Independent Pathways Determine Developmental Dynamics of CpG Island Methylation on the Inactive X Chromosome
title_sort smchd1-dependent and -independent pathways determine developmental dynamics of cpg island methylation on the inactive x chromosome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437444/
https://www.ncbi.nlm.nih.gov/pubmed/22841499
http://dx.doi.org/10.1016/j.devcel.2012.06.011
work_keys_str_mv AT gendrelannevalerie smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT apedaileanwyn smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT cokerheather smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT termanisausma smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT zvetkovailona smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT godwinjonathan smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT tangyamy smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT huntleyderek smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT montanagiovanni smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT taylorsteven smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT giannoulatoueleni smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT heardedith smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT stanchevairina smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome
AT brockdorffneil smchd1dependentandindependentpathwaysdeterminedevelopmentaldynamicsofcpgislandmethylationontheinactivexchromosome