Non-coding roX RNAs prevent the binding of the MSL-complex to heterochromatic regions

PLoS Genet. 2014 Dec 11;10(12):e1004865. doi: 10.1371/journal.pgen.1004865. eCollection 2014 Dec.

Abstract

Long non-coding RNAs contribute to dosage compensation in both mammals and Drosophila by inducing changes in the chromatin structure of the X-chromosome. In Drosophila melanogaster, roX1 and roX2 are long non-coding RNAs that together with proteins form the male-specific lethal (MSL) complex, which coats the entire male X-chromosome and mediates dosage compensation by increasing its transcriptional output. Studies on polytene chromosomes have demonstrated that when both roX1 and roX2 are absent, the MSL-complex becomes less abundant on the male X-chromosome and is relocated to the chromocenter and the 4th chromosome. Here we address the role of roX RNAs in MSL-complex targeting and the evolution of dosage compensation in Drosophila. We performed ChIP-seq experiments which showed that MSL-complex recruitment to high affinity sites (HAS) on the X-chromosome is independent of roX and that the HAS sequence motif is conserved in D. simulans. Additionally, a complete and enzymatically active MSL-complex is recruited to six specific genes on the 4th chromosome. Interestingly, our sequence analysis showed that in the absence of roX RNAs, the MSL-complex has an affinity for regions enriched in Hoppel transposable elements and repeats in general. We hypothesize that roX mutants reveal the ancient targeting of the MSL-complex and propose that the role of roX RNAs is to prevent the binding of the MSL-complex to heterochromatin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Conserved Sequence
  • DNA-Binding Proteins / physiology*
  • Dosage Compensation, Genetic
  • Drosophila Proteins / physiology*
  • Drosophila melanogaster / genetics*
  • Drosophila melanogaster / metabolism
  • Female
  • Heterochromatin / metabolism*
  • Male
  • Nuclear Proteins / physiology*
  • Polytene Chromosomes / metabolism
  • Protein Binding
  • Protein Transport
  • RNA, Untranslated
  • Repetitive Sequences, Nucleic Acid
  • Transcription Factors / physiology*

Substances

  • DNA-Binding Proteins
  • Drosophila Proteins
  • Heterochromatin
  • Nuclear Proteins
  • RNA, Untranslated
  • Transcription Factors
  • msl-1 protein, Drosophila
  • msl-2 protein, Drosophila

Grants and funding

This work was supported by grants from FCT – Fundação para a Ciência e a Tecnologia and the JC Kempe Foundation (MLAF), JC Kempe and Lars Hierta Foundations (PP), the Swedish Research Council (621-2012-2165) and Swedish Cancer Foundation (CAN 2011/382) (JL). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.