Abstract

We reported previously that chicken HIRA, a homolog of Saccharomyces cerevisiae transcriptional co-repressors Hir1p and Hir2p, possesses seven WD dipeptide motifs and an LXXLL motif in its N-terminal and C-terminal halves, respectively, required for transcription regulations. Here, by using the gene targeting technique, we generated the homozygous HIRA-deficient DT40 mutant DeltaHIRA. The HIRA deficiency caused slightly delayed cell growth and affected the opposite transcriptions of cell cycle-related genes, i.e. repressions for P18, CDC25B, and BCL-2, activations for P19 and cyclin A, and histones H2A, H2B, H3, and H4. These altered expressions were completely revived by the artificial stable expression of hemagglutinin-tagged HIRA in DeltaHIRA. The ability to rescue the delayed growth rate was preferentially aided by the N-terminal half instead of the C-terminal half. We cloned the chicken P18 genomic DNA, and we established that its promoter was located surrounding the sequence GCGGGCGC at positions -1157 to -1150. Chromatin immunoprecipitation assay revealed that the N-terminal half interacted directly or indirectly with the putative promoter region of the p18 gene, resulting in up-regulation of the gene. These results indicated that the N-terminal half of HIRA should contribute positively to the growth rate via up-regulation of a set of cell cycle-related genes, whereas the C-terminal half down-regulated another set of them without exhibiting any effect on the cell growth.

Highlights

  • Mutants devoid of PCNA2 binding ability require Hir/Asf-1 proteins [13]

  • This notion is further supported by a finding that CAF-1 and HIRA are contained in the histone H3.1 and H3.3 complexes, respectively [31]

  • We cloned cDNA encoding chicken HIRA, and we demonstrated that WD dipeptide motifs in the N-terminal half of HIRA and an LXXLL motif in the C-terminal half are necessary for its in vitro and in vivo interactions with CAF-1p48 and histone deacetylase-2 (HDAC-2), respectively

Read more

Summary

Introduction

Mutants devoid of PCNA2 binding ability require Hir/Asf-1 (anti-silencing function-1) proteins [13]. The elevated expressions of all core histone genes were mostly suppressed in the presence of full-length HA-tagged HIRA expressed stably in ⌬HIRA cells (cl2-14-p␤-HAHIRAF-6), the mutant cells transfected with vector p␤-HA-2 as a control showed no influence on all these genes (cl2-14-p␤-HA-2), indicating that HIRA surely exhibits the ability to repress the transcriptions of core histone genes.

Results
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