#Id: 6882

#Unit 3. Fundamental Processes

#Id: 6883

#Unit 3. Fundamental Processes

Inactive X chromosome also becomes associated with PRC2 complexes, which catalyze the trimethylation of histone H3 lysine 27. This methylation results in association of the PRC1 complex and transcriptional repression

#Id: 6884

#Unit 3. Fundamental Processes

The DNA of the inactive X also becomes methylated at most of its CpG island promoters. Specialized histone octamers in which histone H2A is replaced by a paralog of H2A called macroH2A also become associated with the inactive X.

#Id: 6885

#Unit 3. Fundamental Processes

DNA methylation and macroH2A contribute to the stable repression of the inactive X chromosome  A. Wutz and J. Gribnau, Curr. Opin. Genet. Dev. 17 (2007): 387–393. inactive specific transcript), which is stably expressed only on the inactive X chromosome.

#Id: 6886

#Unit 3. Fundamental Processes

Recruitment of Polycomb repressor complexes (PRC1 and PRC2), which trigger a series of chromosome-wide histone modifications (H2AK119 ubiquitination, H3K27 methylation, H4K20 methylation, and H4 deacetylation). Late in the process, an inactive X-specific histone variant, macroH2A

#Id: 6887

#Unit 3. Fundamental Processes

Inactivation of the X chromosome in females is governed by the n–1 rule