ALC1 Finds a New Foothold on the Nucleosome's Super-Groove
Bridges, H. R.; Bacic, L.; Deindl, S.; Gaullier, G.
Show abstract
Nucleosomes act as recognition platforms for chromatin-binding factors that coordinate genome maintenance. A distinct structural feature of the nucleosome is the alignment of the DNA major and minor grooves across both gyres, forming continuous major and minor super-grooves. Despite this prominent feature, only one example of a naturally occurring protein binding to a super-groove is documented at the structural level to date. The chromatin remodeler Amplified in Liver Cancer 1 (ALC1) is a key component of the DNA damage response and a promising therapeutic target in cancer. Through extensive classification of our cryo-electron microscopy data, we identified a previously unresolved ALC1-nucleosome complex characterized by a loosely bound conformation of ALC1. This conformation represents an intermediate between the auto-inhibited and active states, and provides new structural insights into the conformational transitions that regulate ALC1 activity. In this intermediate state, the linker of ALC1 engages the nucleosomes minor DNA super-groove across both gyres in a recognition mode observed for the first time in a naturally occurring protein. SynopsisRe-analysis of a publicly available cryo-EM dataset identifies an intermediate state of the oncogenic chromatin remodeler ALC1, revealing the conformational change leading to its activation upon binding to a PARylated nucleosome. The remodeler recognizes the nucleosomes super-groove.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- Exploiting cryo-EM structures of actomyosin-5a to reveal the physical properties of its lever 95%
- A two-site flexible clamp mechanism for RET-GDNF-GFRα1 assembly reveals both conformational adaptation and strict geometric spacing 95%
- Coordination of phage genome degradation versus host genome protection by a bifunctional restriction-modification enzyme visualized by CryoEM 95%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.