Dynamic control of sister chromatid cohesion: How is DNA association of cohesin regulated by Wapl and acetylation

BBSRC · United Kingdom government procurement

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September 29, 2027
Response Due
Active
Status

Opportunity Overview

DNA is a macromolecule present in each cell, which acts as the genetic information carrier in all organisms (from bacteria to humans). This genetic information is passed from parents to their offspring and decides their biological characteristics. During cell proliferation, all of the DNA is precisely duplicated to form identical 'sister DNAs'. Subsequently, the sister DNAs must be accurately separated and equally distributed into the two newborn daughter cells. If anything goes wrong during this process, cells will encounter catastrophic consequences, such as cell death or malfunction. This will lead to cancer and other diseases, for example, developmental disorders. To prevent premature separation and ensure the faithful passing of genetic information from parent cells to daughter cells, the replicated sister DNAs must be held together through a mechanism called sister chromatid cohesion. Only when the cells are fully prepared and the sister DNAs are ready to separate is the sister chromatid cohesion removed, to permit the movement of the sister DNAs to opposite poles of the cell.

Sister chromatid cohesion is achieved through a protein complex called cohesin, which consists of three protein subunits. Besides sister chromatid cohesion, cohesin also plays important roles in compacting DNA, regulating gene expression, and repairing damaged DNA. Though it is responsible for multiple functions on DNA, cohesin actually has a very simple mode to interact with DNA. The three subunits of cohesin form a ring structure and DNA is entrapped within this ring. To enable cohesin to carry out its functions, the ring can open and close, allowing the DNA fiber to get in or out of the ring. Precise regulation of the opening and closing of the ring is fundamental for cohesin's versatile functions. Defects in this regulation compromise cohesin's function, leading in humans to cancer and inherited developmental disorders (such as Cornelia de Lange syndrome and Roberts syndrome).
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Solicitation Details

Issuing agencyBBSRC
CountryUnited Kingdom
CategoryResearch Development
PublishedSeptember 30, 2024
Procurement stageActive solicitation
Response dueSeptember 29, 2027
StatusOpen — accepting responses
Official sourceView original notice
Last verifiedAugust 12, 2026

Source: UK Research and Innovation (UKRI) — Open Government Licence v3.0.

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