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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |