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Published Erratum
. 2016 Feb 4:17:21.
doi: 10.1186/s13059-016-0886-3.

Erratum to: Genome-wide incorporation dynamics reveal distinct categories of turnover for the histone variant H3.3

Daniel C Kraushaar  1 , Wenfei Jin  1 , Alika Maunakea  1 , Brian Abraham  1 , Misook Ha  2 , Keji Zhao  3
Affiliations
Published Erratum

Erratum to: Genome-wide incorporation dynamics reveal distinct categories of turnover for the histone variant H3.3

Daniel C Kraushaar et al. Genome Biol. .
No abstract available

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Figures

Fig. 1
Fig. 1
A versatile system to study replication-independent nucleosome dynamics in mammals. (a) Schematic of TET-inducible expression system to study H3.3 turnover. CMV, cytomegalovirus; rtTA, reverse tetracycline-controlled transactivator; TRE, tetracycline responsive elements. (b) Western blot showing protein levels of transgenic HA/FLAG-H3.3 compared to endogenous H3.3. HA/FLAG-H3.3 expression 24 hours after DOX addition. The band marked with an asterisk is non-specific. The arrow marks transgenic HA/FLAG-H3.3. (c) Time course western blots of HA/FLAG-H3.3 expression. (d) Bromodeoxyuridine (BrdU) immunostaining of NIH/3 T3 cells treated with DNA polymerase inhibitor aphidicolin and DOX across time points of H3.3 induction. DMSO, dimethylsulfoxide. (e) Cell cycle analysis of cells treated with aphidicolin/DOX. Cells were stained with propidium iodide and analyzed by flow cytometry
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Erratum for

References

    1. Kraushaar DC, Jin W, Maunakea A, Abraham B, Ha M, Zhao K. Genome-wide incorporation dynamics reveal distinct categories of turnover for the histone variant H3.3. Genome Biol. 2013;14:R121. doi: 10.1186/gb-2013-14-10-r121. - DOI - PMC - PubMed

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