USC researchers discover key aspect in gene activation

USC researchers discover key aspect in gene activation

9:46 PM, 16th November 2011
USC researchers discover key aspect in gene activation

LOS ANGELES, US: Researchers at the Keck School of Medicine of USC have discovered key processes by which estrogen, the female sex hormone, activates genes in breast cancer cells. A greater understanding of how this occurs is expected to eventually lead to new treatments for the disease.

Michael R Stallcup, Professor and Chair, Keck School’s Department of Biochemistry and Molecular Biology, was the Senior author. Kwang Won Jeong, Postdoctoral Student in Stallcup’s lab, was the first author of the paper, which was published online Nov 13 in the journal Nature Structural & Molecular Biology.

The researchers found that a protein, TIP60, recognizes when a common chemical process called methylation occurs in chromatin, the material that enfolds all genes. Methylation controls how genes are folded in the complex structure of chromatin, which determines whether the genes are active or inactive.

After recognizing the methylation signal, the researchers discovered that TIP60 then binds to the signal, connecting TIP60 to chromatin and then changing chromatin’s structure, which helps to activate the gene. The methylation that TIP60 recognizes is generated by MLL1, another protein.

“It’s like when you’re in your car and come to a red light,” said Stallcup. “The light doesn’t make you stop, but it is a signal that you have to interpret and then decide to stop. In this case, the methylation modification that TIP60 recognizes is one of those signals and then TIP60 acts on that signal.”

The findings build upon previous work of Stallcup’s lab. Earlier published research revealed that the methylation of chromatin and other proteins plays several important roles in controlling the activities of genes.

While the recent findings are significant, Stallcup stressed that there is much more to be discovered. “We want to understand more about other steps in the process of gene activation,” said Stallcup. “In particular, we’re interested in the function of the MLL1 protein because we think it plays a key role in controlling chromatin structure and folding, which we think is critical for activation of genes by estrogen.”

Stallcup also noted that estrogen regulates just a few hundred of the tens of thousands of genes in every human cell, but that the research has broader implications. “While the process we’re studying is the regulation of gene activity by estrogen, the findings have potentially global significance because the methylation modification of chromatin that TIP60 recognizes is found in all active and potentially active genes in human cells,” he said.

© The University of Southern California News

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