The methyl-CpG binding protein 2 (MeCP2) is a ubiquitous transcription factor predominantly expressed in the brain and mutated in Rett syndrome, a progressive neurodevelopmental disorder. Neuronal MeCP2 genome-wide binding tracks methyl-CpG density and its absence results in large-scale changes in chromatin structures, suggesting a global regulatory role. In mouse cells MeCP2 accumulates at pericentric heterochromatin (PCH), composed by major satellite DNA of different chromosomes that aggregate to form chromocenters, structures possibly critical for the establishment of silent compartments. Several proteins and ncRNAs [e.g. HP1s and maj sat forward transcript (MSFT)] seem to be relevant for establishment and maintenance of PCH. Recently, we highlighted a crucial role of MeCP2 in the PCH re-organization during neural differentiation, supporting the view of MeCP2 as a multifunctional chromatin organizing factor. To unravel the molecular mechanism by which MeCP2 regulates the PCH re-organization we investigated the spatial distribution of MSFT and HP1 alpha during neural differentiation of wt and MeCP2-/y cells. MSFT expression increases during differentiation of both cell lines and strong MSFT RNA-FISH signals are visible at chromocenters of wt differentiated cells, whereas the signals appeared weaker in MeCP2-/y nuclei. Noteworthy, the foci number in wt nuclei is greater compared to MeCP2-/y nuclei. Moreover, MeCP2 co-localizes and physically associates with MSFT. These data point out a contribution of MeCP2 in the sub-nuclear localization of MSFT. On the other hand, RNAse treatment causes delocalization of MeCP2 from the chromocenters, suggesting a role of RNAs in MeCP2 positioning. Furthermore, HP1 alpha co-localizes with MeCP2 and MSFT at chromocenters. A deeper analysis of HP1s distribution in MeCP2-/y cells is currently under investigation. Our preliminary data allow to speculate that MeCP2 may cooperate with MSFT and HP1s, for the PCH organization.
MeCP2 is required for major satellite forward transcript recruitment at pericentric heterochromatin during neural differentiation
Floriana Della Ragione;Maria Rosaria Matarazzo;Maurizio D'Esposito
2015
Abstract
The methyl-CpG binding protein 2 (MeCP2) is a ubiquitous transcription factor predominantly expressed in the brain and mutated in Rett syndrome, a progressive neurodevelopmental disorder. Neuronal MeCP2 genome-wide binding tracks methyl-CpG density and its absence results in large-scale changes in chromatin structures, suggesting a global regulatory role. In mouse cells MeCP2 accumulates at pericentric heterochromatin (PCH), composed by major satellite DNA of different chromosomes that aggregate to form chromocenters, structures possibly critical for the establishment of silent compartments. Several proteins and ncRNAs [e.g. HP1s and maj sat forward transcript (MSFT)] seem to be relevant for establishment and maintenance of PCH. Recently, we highlighted a crucial role of MeCP2 in the PCH re-organization during neural differentiation, supporting the view of MeCP2 as a multifunctional chromatin organizing factor. To unravel the molecular mechanism by which MeCP2 regulates the PCH re-organization we investigated the spatial distribution of MSFT and HP1 alpha during neural differentiation of wt and MeCP2-/y cells. MSFT expression increases during differentiation of both cell lines and strong MSFT RNA-FISH signals are visible at chromocenters of wt differentiated cells, whereas the signals appeared weaker in MeCP2-/y nuclei. Noteworthy, the foci number in wt nuclei is greater compared to MeCP2-/y nuclei. Moreover, MeCP2 co-localizes and physically associates with MSFT. These data point out a contribution of MeCP2 in the sub-nuclear localization of MSFT. On the other hand, RNAse treatment causes delocalization of MeCP2 from the chromocenters, suggesting a role of RNAs in MeCP2 positioning. Furthermore, HP1 alpha co-localizes with MeCP2 and MSFT at chromocenters. A deeper analysis of HP1s distribution in MeCP2-/y cells is currently under investigation. Our preliminary data allow to speculate that MeCP2 may cooperate with MSFT and HP1s, for the PCH organization.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
