The mammalian interphase chromatin responds to DNA damages by altering the compactness of its architecture, thereby permitting local access of DNA repair machineries. Adding to the cellular strategies of chromatin remodeling following DNA damage, our recent work identified the 53BP1-EXPAND1 module in promoting chromatin dynamics in response to DNA double-strand breaks. Endowed with a nucleosome-binding PWWP domain, EXPAND1 tethers to the chromatin where it is involved in maintaining basal chromatin accessibility in unperturbed cells. Interestingly, through its direct interaction with the DNA damage mediator protein 53BP1, EXPAND1 accumulates at the damage-modified chromatin and triggers its further decondensation. These observations, togeth...
Spatial distribution of DNA damage response (DDR) machineries at the damaged chromatin provides imp...
53BP1 plays multiple roles in mammalian DNA damage repair, mediating pathway choice and facilitating...
Understanding how DNA repair processes occur in vivo when access to DNA is hindered by chromatin str...
Dynamic changes of chromatin structure facilitate diverse biological events, including DNA replicati...
Upon DNA damage, p53-binding protein 1 (53BP1) relocalizes to sites of DNA double-strand breaks and ...
To safeguard genome integrity in response to DNA double-strand breaks (DSBs), mammalian cells mobili...
53BP1 is a multi-domain DNA damage response factor containing a chromatin-binding tudor domain, an o...
The tumour suppressor p53 has an essential role in maintaining the genomic integrity of the mammalia...
Chromatin structure is dynamically reorganized at multiple levels in response to DNA double-strand b...
Cellular DNA is constantly challenged by damage-inducing factors derived from exogenous or endogenou...
The mechanisms that localise 53BP1 to sites of DNA double-strand breaks (DSBs) have remained elusive...
The protein p53 binding protein one (53BP1) was discovered in a yeast two-hybrid screen that used th...
Chromatin structure modulates the rate of DNA damage formation and repair in different regions of eu...
In eukaryotes, genomic DNA is tightly compacted into a protein-DNA complex known as chromatin. This ...
Summary53BP1 plays multiple roles in mammalian DNA damage repair, mediating pathway choice and facil...
Spatial distribution of DNA damage response (DDR) machineries at the damaged chromatin provides imp...
53BP1 plays multiple roles in mammalian DNA damage repair, mediating pathway choice and facilitating...
Understanding how DNA repair processes occur in vivo when access to DNA is hindered by chromatin str...
Dynamic changes of chromatin structure facilitate diverse biological events, including DNA replicati...
Upon DNA damage, p53-binding protein 1 (53BP1) relocalizes to sites of DNA double-strand breaks and ...
To safeguard genome integrity in response to DNA double-strand breaks (DSBs), mammalian cells mobili...
53BP1 is a multi-domain DNA damage response factor containing a chromatin-binding tudor domain, an o...
The tumour suppressor p53 has an essential role in maintaining the genomic integrity of the mammalia...
Chromatin structure is dynamically reorganized at multiple levels in response to DNA double-strand b...
Cellular DNA is constantly challenged by damage-inducing factors derived from exogenous or endogenou...
The mechanisms that localise 53BP1 to sites of DNA double-strand breaks (DSBs) have remained elusive...
The protein p53 binding protein one (53BP1) was discovered in a yeast two-hybrid screen that used th...
Chromatin structure modulates the rate of DNA damage formation and repair in different regions of eu...
In eukaryotes, genomic DNA is tightly compacted into a protein-DNA complex known as chromatin. This ...
Summary53BP1 plays multiple roles in mammalian DNA damage repair, mediating pathway choice and facil...
Spatial distribution of DNA damage response (DDR) machineries at the damaged chromatin provides imp...
53BP1 plays multiple roles in mammalian DNA damage repair, mediating pathway choice and facilitating...
Understanding how DNA repair processes occur in vivo when access to DNA is hindered by chromatin str...