Some patterns of histone methylation are linked to human gene activation, and other patterns are linked to gene repression. By combining chromatin immunoprecipitation with new Solexa 1G sequencing technology, Artem Barski at the National Institutes of Health and colleagues from the University of California, Los Angeles, generated genome-wide maps for histone methylations and correlated methylation events with different levels of gene expression.1 The researchers saw differences in methylation patterns between stem cells and differentiated T cells, and they correlated certain methylations with chromosome breakpoints involved in T cell cancers.

"The sheer 'comprehensiveness' of this study is really what makes it important," says Steven Henikoff, a member of the Faculty of 1000 and a researcher at the Fred Hutchinson Cancer Research Center. "This paper couldn't have been written six months ago, because the technology wasn't there." Barski's group applied the new technique systematically, sequencing shorter sequences (36 bp) of DNA from human nucleosomes.

The analysis will be important for annotating genes. "These modifications are great markers for detecting the underlying processes of what's going on," Henikoff says. If you're looking at only gene expression levels, "you're seeing it all filtered through the complicated processes of transcriptional initiation and elongation, and mRNA processing, transport, and stabilization," he says.

1. A. Barski et al., "High-resolution profiling of histone methylations in the human genome," Cell, 129:823?37, May 18, 2007. | [PubMed]

These papers were selected from multiple disciplines from the Faculty of 1000, a web-based literature awareness tool (www.f1000biology.com).



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