Cistromes
In PNAS, Dongyin Guan and Mitchell A. Lazar commented on work by Fei et al., concluding that "noncoding mutations in enhancers and other, less well-characterized, TF [transcription factor] binding regions also have large effects on cell survival and proliferation." Their review, "Shining light on dark matter in the genome," begins,
The complexity of multicellular organisms requires the genome to be transcribed in a cell-type-dependent manner that is responsive to signals, such as hormones, from the internal environment. This is mediated by the epigenome, which decorates and organizes the genome in a web of modified histone proteins functioning in nucleosomes and chemical modifications to genomic DNA arranged 3-dimensionally in the cell nucleus. Functional features of the epigenome such as acetylation of histone lysine residues are "read" by specialized proteins such as those containing bromodomains. Likewise, the genome itself is read by proteins known as sequence-specific transcription factors (TFs), which recognize and bind to specific motifs in genomic DNA. The totality of these sites for a given transcription factor in a given cell is known as its "cistrome". Most of these binding sites occur in the ∼99% of the genome that does not encode for proteins. [Emphasis added.]













Comment: It is a shame that most conventional microbiology seems to start with the unspoken assumption that Nature is wasteful and arbitrary whenever it comes up against something it doesn't immediately comprehend. Hence the terms 'junk' and 'parasite' for misunderstood DNA structures. How much quicker would the science progress if they took the stance as Paul Nelson has: "If it works, it's not happening by accident."