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HP1 is a well known conserved protein involved in heterochromatin formation and gene silencing in different species including humans1-4. A general model has been proposed for heterochromatin formation and epigenetic gene silencing in different species that implies an essential role for HP1. According to the model, histone methyltransferase enzymes (HMTases) methylate the histone H3 at lysine 9 (H3-MeK9), creating selective binding sites for itself and the chromodomain of HP15. This complex is thought to form a higher order chromatin state that represses gene activity. It has also been found that HP1 plays a role in telomere capping6. Surprisingly, recent data have suggested an association of HP1 in gene activity7-10 but the nature of this interaction is still completely obscure. Here we show, that HP1 is required for positive regulation of more than one hundred euchromatic genes by its association with the corresponding RNA transcripts and by its interaction with the well known proteins DDP111, HRB87F12 and PEP13, which belong to different classes of heterogeneous nuclear ribonucleoproteins (hnRNPs) involved in RNA processing . We also found that all these hnRNP proteins also bind heterochromatin and are dominant suppressors of position effect variegation. Our data together, show novel and unexpected functions for HP1 and hnRNPs proteins. All these proteins are in fact involved in both RNA transcript processing and in heterochromatin formation. This suggests that, in general, similar epigenetic mechanisms have a significant role in the metabolism of both RNA and heterochromatin.

The Heterochromatin Protein 1 positively regulates euchromatic gene expression by RNA binding