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Barrier-to-autointegration factor (BAF) involvement in prelamin A-related chromatin organization changes.


ABSTRACT: Chromatin disorganization is one of the major alterations linked to prelamin A processing impairment. In this study we demonstrate that BAF is necessary to modulate prelamin A effects on chromatin structure. We show that when prelamin A and BAF cannot properly interact no prelamin A-dependent effects on chromatin occur; similar to what is observed in human Nestor Guillermo Progeria Syndrome cells harboring a BAF mutation, in HEK293 cells expressing a BAF mutant unable to bind prelamin A, or in siRNA mediated BAF-depleted HEK293 cells expressing prelamin A. BAF is necessary to induce histone trimethyl-H3K9 as well as HP1-alpha and LAP2-alpha nuclear relocalization in response to prelamin A accumulation. These findings are enforced by electron microscopy evaluations showing how the prelamin A-BAF interaction governs overall chromatin organization. Finally, we demonstrate that the LAP2-alpha nuclear localization defect observed in HGPS cells involves the progerin-BAF interaction, thus establishing a functional link between BAF and prelamin A pathological forms.

SUBMITTER: Loi M 

PROVIDER: S-EPMC4941268 | biostudies-literature | 2016 Mar

REPOSITORIES: biostudies-literature

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Barrier-to-autointegration factor (BAF) involvement in prelamin A-related chromatin organization changes.

Loi Manuela M   Cenni Vittoria V   Duchi Serena S   Squarzoni Stefano S   Lopez-Otin Carlos C   Foisner Roland R   Lattanzi Giovanna G   Capanni Cristina C  

Oncotarget 20160301 13


Chromatin disorganization is one of the major alterations linked to prelamin A processing impairment. In this study we demonstrate that BAF is necessary to modulate prelamin A effects on chromatin structure. We show that when prelamin A and BAF cannot properly interact no prelamin A-dependent effects on chromatin occur; similar to what is observed in human Nestor Guillermo Progeria Syndrome cells harboring a BAF mutation, in HEK293 cells expressing a BAF mutant unable to bind prelamin A, or in s  ...[more]

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