Abstract

In budding yeast, the Sir2, Sir3 and Sir4 proteins form SIR complexes, required for the assembly of silent heterochromatin domains, and which mediate transcription silencing at the telomeres as well as at silent mating type loci. In this study, under fluorescence microscopy, we found most Sir3-GFP expressions in the logarithmic phase cells appeared as multiple punctations as expected. However, some differences in the distribution of fluorescent signals were detected in the diauxic∼early stationary phase cells. To clarify these, we then used ChIP on chip assays to investigate the genome-wide localization of Sir3. In general, Sir3 binds to all 32 telomere proximal regions, the silent mating type loci and also binds to the rDNA region. However, the genome-wide localization patterns of Sir3 are different between these two distinct growth phases. We also confirmed that Sir3 binds to a recently identified secondary binding site, PAU genes, and further identified 349 Sir3-associated cluster regions. These results provide additional support in roles for Sir3 in the modulation of gene expression during physical conditions such as diauxic∼early stationary phase growing. Moreover, they imply that Sir3 may be not only involved in the formation of conventional silent heterochromatin, but also able to associate with some other chromatin regions involved in epigenetic regulation.

Highlights

  • In the eukaryotic nucleus, genomic DNA is packaged into together form a nucleosome-binding complex, called SIR complex chromatin

  • We mainly focused on two distinct growth phases: the logarithmic and diauxic~early stationary phases

  • We found that the genome-wide localization patterns of Sir3 were different from those at these two distinct growth stages, and further analyzed our newly identified Sir3-associated cluster regions in diauxic~early stationary phase cells

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Summary

Introduction

Genomic DNA is packaged into together form a nucleosome-binding complex, called SIR complex chromatin. We found that the genome-wide localization patterns of Sir3 were different from those at these two distinct growth stages, and further analyzed our newly identified Sir3-associated cluster regions in diauxic~early stationary phase cells.

Results
Conclusion

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