Chromatin dynamics and gene positioning.

The mammalian cell nucleus provides a landscape where genes are regulated through their organization and association with freely diffusing proteins and nuclear domains. In many cases, specific genes are highly dynamic, and the principles governing their movements and interchromosomal interactions are currently under intensive study. Recent investigations have implicated actin and myosin in chromatin dynamics and gene expression. Here, we discuss our current understanding of the dynamics of the interphase genome and how it impacts nuclear organization and gene activity.

Dynamics and anchoring of heterochromatic loci during development.

Positioning a euchromatic gene near heterochromatin can influence its expression. To better understand expression-relevant changes in locus positioning, we monitored in vivo movement of centromeres and a euchromatic locus (with and without a nearby insertion of heterochromatin) in developing Drosophila tissue. In most undifferentiated nuclei, the rate of diffusion and step size of the locus is unaffected by the heterochromatic insertion. Interestingly, although the movement observed here is non directional, the heterochromatic insertion allows the flanking euchromatic region to enter and move within the heterochromatic compartment. This study also finds that a constraint on chromatin movement is imposed which is a factor of distance from the centric heterochromatic compartment. This restraint prevents the heterochromatic locus from moving away from the centric heterochromatin compartment. Therefore, because of the constraint, even distinct and non-random nuclear organizations can be attained from random chromatin movements. We also find a general constraint on chromatin movement is imposed during differentiation, which stabilizes changes in nuclear organization in differentiated nuclei.

Changing chromatin dynamics and nuclear organization during differentiation in Drosophila larval tissue.

Global changes in gene expression and exit from the cell cycle underlie differentiation. Therefore, understanding chromatin behavior in differentiating nuclei and late G1 is key to understanding this developmental event. A nuclear event that has been shown to specifically occur in late G1 is the association of two heterochromatic blocks in Drosophila. The brown(Dominant) (bw(D)) chromosome of Drosophila melanogaster contains a large block of heterochromatin near the end of 2R. This distal block associates with centric heterochromatin (2Rh), but not until at least 5 hours into G1. We used the bw(D) allele as a model for nuclear organization to determine whether its association with the heterochromatic compartment of the second chromosomes (2Rh) strictly requires differentiation or if this change is a stochastic event, its occurrence being proportional to time spent in G1/G0 phase of the cell cycle. Fluorescence in situ hybridization on eye imaginal discs showed increased association between the bw locus and 2Rh in differentiated cells. Interestingly, an increase in the number of nuclei showing bw(D)-2Rh association in the brains of developmentally delayed larvae that were compromised for differentiation was also observed. Live fluorescence imaging showed that the kinetics of chromatin movement remains unchanged in the developmentally arrested nuclei. These observations suggest that nuclear reorganization is not directly controlled by specific inductive signals during differentiation and that this nuclear reorganization can happen in a cell, regardless of differentiation state, that is arrested in the appropriate cell cycle stage. However, we did see changes that appear to be more directly correlated with differentiation. Dynamic imaging in eye imaginal discs showed that the movement of chromatin is more constrained in differentiated cells, implying that confinement of loci to a smaller nuclear space may help to maintain the changed organization and the transcription profile that accompanies differentiation.