Interestingly, Grewal and his colleagues showed that deleting "boundary elements" which mark the transition between silent and active regions of DNA allowed the spreading of lysine 9-methylated histones into neighboring DNA normally occupied by lysine 4-methylated histones. This finding has important implications for many types of genetic disease. It indicates that damage to a boundary element in a critical region of a chromosome could lead to abnormal silencing or the switching off of genes in that chromosomal region, with potentially serious consequences.
David Allis (University of Virginia), Grewal's colleague in this and another study published earlier this year in Science, has proposed that in addition to the now familiar genetic code of repeating As, Cs, Gs, and Ts in the sequence of DNA, a "histone code" exists in which differentially modified histone proteins can organize the genome into active and silent regions that can be stably inherited.
Indeed, working at the National Cancer Institute in 1996, Grewal and former Cold Spring Harbor Laboratory scientist Amar Klar showed that active and silent chromosomal states can be stably inherited through mitosis (cell division) and, remarkably, through meiosis (the production of gametes such as egg and sperm). In essence, Grewal and Klar found that the Mendelian inheritance of traits sometimes depends not only on the faithful replication of DNA sequences, but also on the transmission of "higher order" chromosome structure. In a study published in journal Cell last year, Grewal and colleagues went on to show that the "gene" in these instances is not only DNA, but DNA plus associated proteins. The scientists proposed a chromosome replication model in which both the DNA molecule plus higher order chromosome structure are duplicated.
The new study in Science is one of several that are beginning to elucidate the role of histones and other proteins in such a chromosome replication process.