Abstract

Heterochromatin preferentially assembles at repetitive DNA elements, playing roles in transcriptional silencing, recombination suppression, and chromosome segregation. The RNAi machinery is required for heterochromatin assembly in a diverse range of organisms. In fission yeast, RNA splicing factors are also required for pericentric heterochromatin assembly, and a prevailing model is that splicing factors provide a platform for siRNA generation independently of their splicing activity. Here, by screening the fission yeast deletion library, we discovered four novel splicing factors that are required for pericentric heterochromatin assembly. Sequencing total cellular RNAs from the strongest of these mutants, cwf14Δ, showed intron retention in mRNAs of several RNAi factors. Moreover, introducing cDNA versions of RNAi factors significantly restored pericentric heterochromatin in splicing mutants. We also found that mutations of splicing factors resulted in defective telomeric heterochromatin assembly and mis-splicing the mRNA of shelterin component Tpz1, and that replacement of tpz1+ with its cDNA partially rescued heterochromatin defects at telomeres in splicing mutants. Thus, proper splicing of RNAi and shelterin factors contributes to heterochromatin assembly at pericentric regions and telomeres.

Highlights

  • Eukaryotic genomic DNA associates with histone and nonhistone proteins to form chromatin, which is necessary for the spatial and temporal organization of chromosomes

  • Factors involved in proper RNA splicing are required for heterochromatin assembly, and it was proposed that splicing factors provide a platform for the recruitment of RNA interference (RNAi) complexes independently of their role in regulating splicing

  • We found several novel splicing factors involved in heterochromatin assembly

Read more

Summary

Introduction

Eukaryotic genomic DNA associates with histone and nonhistone proteins to form chromatin, which is necessary for the spatial and temporal organization of chromosomes. Heterochromatin is highly condensed and often forms over repetitive DNA elements such as transposons. The formation of heterochromatin prevents expression of transposons, improper recombination of repetitive genomic loci, and missegregation of chromosomes during mitosis and meiosis, maintaining genome stability [1,2]. HP1 subsequently recruits diverse proteins to regulate cellular processes such as transcriptional silencing, recombination suppression, and chromosome segregation [1]. Recent work has shown that DNA repeats are transiently transcribed, and the transcripts are processed by the RNA interference (RNAi) machinery into small interfering RNAs (siRNAs), which help target histone-modifying enzymes to repeat regions. The mechanistic details of RNAi-mediated heterochromatin assembly is not yet well understood [12,13,14]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call