Completed Genetics & Molecular Biology Cells, Biochemistry & Physiology

Structure and mechanism of the Ino80 chromatin remodelling complex

In plain English

AI plain-English summary

Every cell in the human body must unspool its tightly packed DNA to read the genes inside, and a protein machine called INO80 does the heavy lifting—but no one knows exactly how it works. The problem is that DNA is wound around spool-like proteins called nucleosomes, and INO80 is one of the few machines that can slide these spools along the DNA to expose genes for copying or repair. Despite its importance, the complex is poorly understood at the molecular level: it contains many subunits with unknown jobs, it requires two copies of itself to move a single nucleosome, and it can somehow sense nearby nucleosomes to space them evenly. This project aims to map the structure of INO80 and determine how its parts work together. If successful, it will reveal the fundamental mechanics of how cells access their own genome—a process that goes wrong in many cancers and developmental disorders. This is fundamental science: there is no immediate practical application, but understanding how INO80 operates could eventually point toward new ways to correct faulty gene access in disease.

View original technical description
Compaction of the genome into chromatin helps to protect the genetic material but also causes problems in regard to access for essential processes such as transcription, replication and repair. Chromatin remodelling complexes alter the state of chromatin through a number of processes that includes chemical modifications of nucleosomes and sliding their position on DNA. Nucleosome sliding is catalysed by a number of protein complexes, one of which is the multi-subunit INO80 complex. INO80 contains an ATP-dependent translocase motor, that is common to all nucleosome sliders, but also a variety of other subunits, most of which have unknown roles. Furthermore, not only does it require two INO80 complexes interacting with a single nucleosome to promote sliding, but the complex also has an ability to “sense” the presence of other nucleosomes to space them evenly on DNA indicating interactions with multiple nucleosomes. The mechanism for this process is poorly understood, particularly at a molecular and structural level. INO80 is highly regulated in several distinct ways, including chemical modifications, small molecule effectors and subunit interactions but none of these are well understood. Finally, how the various subunits, many of which are ATPases in their own right, contribute to INO80 activities is also unclear.

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Researchers

Dale Wigley (EPMC Awardee)

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Original classification

Investigator Award in Science

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