Commentary 839
IntroductionHuman cells contain 46 chromatin fibres, i.e. the chromosomes, with a total length of ~5 cm of nucleosomal filaments arranged like beads on a string. Packaging this in an interphase nucleus of typically 5-20 m in diameter requires extensive folding. In the past decades, considerable evidence was accumulated showing that chromatin folding is closely related to genome function. Tightly packed and transcriptionally silent heterochromatin, and more-open transcriptionally active euchromatin represent two classic folding states. In the past decade, we started to see some first principles of chromatin folding. One is that individual chromosomes occupy discrete domains in the interphase nucleus -named chromosome territories -which intermingle only to a limited extent (Cremer and Cremer, 2010). Similarly, different parts of a chromosome also only interact very little (Dietzel et al., 1998;Goetze et al., 2007a;Goetze et al., 2007b). Another organisational principle is based on the finding that mammalian interphase chromosomes are made up of a large number of structural domains, each of which are on averagẽ 1 Mb, that correspond to DNA replication units (Ryba et al., 2010). Furthermore, recent experimental data show that chromatin loops mediated by specific chromatin-chromatin interactions are an important aspect of chromatin organisation, because they bring together distant regulatory elements that control gene expression, such as promoters and enhancers (Carter et al., 2002;Kadauke and Blobel, 2009). Methods that are based on the chromosome conformation capture (3C) technology, which determines two distant genomic sequence elements that are in close proximity in the nucleus (Simonis et al., 2007), have revealed the presence of a large number of intra-chromosomal chromatin-chromatin interactions. The resulting loops vary in length from a few kb to up to tens of Mb and are different in different cell types (Lieberman-Aiden et al., 2009;Simonis et al., 2006). Moreover, it has been shown for many loci that changes in transcriptional activity are tightly correlated with changes in folding (Sproul et al., 2005). Together, these observations show that packaging of the chromatin fibre in the interphase nucleus is closely related to genome function and that loops are a prominent feature of interphase chromatin.The notion that chromatin loops are important for overall genome organisation is also supported from the perspective of polymer models. Recent polymer modelling efforts show that the formation of loops can endow polymers such as chromatin with properties that explain several of its key properties, including chromatin compaction and compartmentalisation. The importance of polymer models is that they aim to explain properties of chromatin on the basis of physical principles and discard those models that do not fulfil this criterion. They make precise predictions that can be tested experimentally and their outcome can be used to further improve the model, thereby increasing our understanding of chro...