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Article Dans Une Revue Biochemistry and Cell Biology Année : 2017

Histone H3.3 regulates mitotic progression in mouse embryonic fibroblasts

Aysegul Ors
  • Fonction : Auteur
Christophe Papin
Bertrand Favier
  • Fonction : Auteur
Yohan Roulland
  • Fonction : Auteur
Defne Dalkara
  • Fonction : Auteur
Mehmet Ozturk
  • Fonction : Auteur
Stefan Dimitrov
Kiran Padmanabhan
  • Fonction : Auteur

Résumé

H3.3 is a histone variant that marks transcription start sites as well as telomeres and heterochromatic sites on the genome. The presence of H3.3 is thought to positively correlate with the transcriptional status of its target genes. Using a conditional genetic strategy against H3.3B, combined with short hairpin RNAs against H3.3A, we essentially depleted all H3.3 gene expression in mouse embryonic fibroblasts. Following nearly complete loss of H3.3 in the cells, our transcriptomic analyses show very little impact on global gene expression or on the localization of histone variant H2A.Z. Instead, fibroblasts displayed slower cell growth and an increase in cell death, coincident with large-scale chromosome misalignment in mitosis and large polylobed or micronuclei in interphase cells. Thus, we conclude that H3.3 may have an important under-explored additional role in chromosome segregation, nuclear structure, and the maintenance of genome integrity.

Dates et versions

hal-03484321 , version 1 (17-12-2021)

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Citer

Ali Hamiche, Aysegul Ors, Christophe Papin, Bertrand Favier, Yohan Roulland, et al.. Histone H3.3 regulates mitotic progression in mouse embryonic fibroblasts. Biochemistry and Cell Biology, 2017, 95 (4), pp.491-499. ⟨10.1139/bcb-2016-0190⟩. ⟨hal-03484321⟩
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