- Histone proteins play a crucial role in DNA packaging.
- It has been thought that proteins called “replication-dependent histone isoforms” all behaved the same way.
- This study shows that proteins in the group vary in expression, and that their dysregulation might influence cancer development.
The findings by researchers at the Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (OSUCCC – James) indicate that replication-dependent histone isoforms can have distinct cellular functions, and that changes in expression of the various isoforms might play a role in cancer development.
The study is published in the journal Nucleic Acids Research as a Breakthrough Article, placing it among the top 2-3 percent of papers presented by the journal in terms of significance and excellence.
“Replication-dependent histone isoforms have always been thought to be functionally identical, but we show that they have distinct functions, and that altering the levels of these isoforms can influence cell proliferation and tumor development,” says principal investigator Mark Parthun, PhD, professor of Molecular and Cellular Biochemistry and a member of the OSUCCC – James Experimental Therapeutics Program.
“These highly novel results provide a new mechanism for the regulation of chromatin structure, Parthun says.”
Replication-dependent histones are highly expressed just before the onset of DNA replication during the cell cycle, and they are repressed when DNA replication is completed.
The genes that encode these histones are located in large clusters that can contain dozens of histone genes. “This localization in gene clusters led to the belief that these histones are regulated as a group, and that the multiple genes encoding each histone are functionally equivalent,” Parthun says.
However, the proteins encoded by replication-dependent histone genes are not identical. For example, 16 genes encode the replication-dependent histone called H2A. Strikingly, these genes encode 11 distinct protein variations.
Parthun and his colleagues conducted the study using three bladder-cancer cell lines. Key findings include:
The abundance of replication-dependent histone H2A isoforms showed dramatic differences in bladder cancer cells vs. normal bladder cells;
Replication-dependent H2A isoforms were expressed at different levels in cancer cells; expression of one isoform was 10-fold higher than the others;
Knocking down the messenger RNA of a specific replication-dependent H2A isoform increased cell proliferation and tumorigenicity.
Replication-dependent H2A isoforms show evidence of individualized regulation.
Funding from the NIH/National Cancer Institute (grant CA101956, CA107106) and the Leukemia and Lymphoma Society supported this research.
Other researchers involved in this study were Rajbir Singh, Amir Mortazavi, Kelly H. Telu, Prabakaran Nagarajan, David M. Lucas, Jennifer M. Thomas-Ahner, Steven K. Clinton, John C. Byrd and Michael A. Freitas, The Ohio State University.
The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute strives to create a cancer-free world by integrating scientific research with excellence in education and patient-centered care, a strategy that leads to better methods of prevention, detection and treatment. Ohio State is one of only 41 National Cancer Institute (NCI)-designated Comprehensive Cancer Centers and one of only four centers funded by the NCI to conduct both phase I and phase II clinical trials. The NCI recently rated Ohio State’s cancer program as “exceptional,” the highest rating given by NCI survey teams. As the cancer program’s 228-bed adult patient-care component, The James is a “Top Hospital” as named by the Leapfrog Group and one of the top cancer hospitals in the nation as ranked by U.S.News & World Report.
A high quality JPEG of Mark Parthun, PhD, is available here.
Contact: Darrell E. Ward, Wexner Medical Center Public Affairs and Media Relations,