Active Genetics & Molecular Biology Cells, Biochemistry & Physiology

Uncovering the cancer specific essentiality of SS18L2, a chromatin regulator of cell cycle

In plain English

AI plain-English summary

A tiny protein called SS18L2, just 77 amino acids long, appears to be essential for cancer cells to divide, and knocking it out stops them in their tracks. This matters because current cancer treatments often damage healthy cells along with cancerous ones. SS18L2 is a chromatin regulator—a protein that controls how DNA is packaged and read—and its role in cell division was only recently discovered through genome-wide CRISPR screens. The researcher aims to uncover exactly how SS18L2 controls the cell cycle, using advanced techniques to track its activity in space and time. Understanding this mechanism could reveal a new vulnerability specific to cancer cells. If successful, this fundamental science project would bridge two previously separate fields—chromatin regulation and cell cycle biology—showing they are deeply interconnected. There is no immediate practical application. But similar fundamental discoveries about how cells control division have historically led to targeted cancer therapies. A deeper understanding of SS18L2’s role could eventually point toward a drug that selectively blocks cancer cell proliferation without harming normal tissue.

View original technical description
SS18L2, a small protein of 77 amino acids and a member of the SNH-protein family, was newly described as an essential gene regulating cell cycle-related processes through epigenome-wide CRISPR/Cas9 library-mediated knockout screens. Cells knocked-out of SS18L2 were observed to arrest at the G2/M transition and showed aberrant mitotic spindle formation and cell size. Many genes regulating the cell cycle progression were observed to be downregulated upon knockout. I propose the application of multiple state-of-the-art techniques in novel set-ups to spatio-temporally resolve the mechanisms by which SS18L2 regulates cell cycle. The description of new chromatin regulation mechanisms and characterization of SS18L2 will be achieved through this project. The interactions uncovered by this study will bring chromatin regulation and cell cycle biology fields together. I aim to reveal a holistic perspective on the interplay between epigenetics and cell cycle regulation, demonstrating that these fields are interconnected rather than existing in mutually exclusive contexts.

View the original record at the funder ↗

Researchers

Ozlem Yedier Bayram (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Tumor suppression by chromatin regulators.
Studying the consequences of chromatin disruption in Cornelia de Lange Syndrome
CDK-containing macromolecular assemblies
Genetic approaches to dissect the role of cohesin in gene regulation.
Global Cellular Controls in Fission Yeast

Original classification

Early-Career Award

Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.