دورية أكاديمية

HIRA vs. DAXX: the two axes shaping the histone H3.3 landscape

التفاصيل البيبلوغرافية
العنوان: HIRA vs. DAXX: the two axes shaping the histone H3.3 landscape
المؤلفون: Jinmi Choi, Taewan Kim, Eun-Jung Cho
المصدر: Experimental and Molecular Medicine, Vol 56, Iss 2, Pp 251-263 (2024)
بيانات النشر: Nature Publishing Group, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
LCC:Biochemistry
مصطلحات موضوعية: Medicine, Biochemistry, QD415-436
الوصف: Abstract H3.3, the most common replacement variant for histone H3, has emerged as an important player in chromatin dynamics for controlling gene expression and genome integrity. While replicative variants H3.1 and H3.2 are primarily incorporated into nucleosomes during DNA synthesis, H3.3 is under the control of H3.3-specific histone chaperones for spatiotemporal incorporation throughout the cell cycle. Over the years, there has been progress in understanding the mechanisms by which H3.3 affects domain structure and function. Furthermore, H3.3 distribution and relative abundance profoundly impact cellular identity and plasticity during normal development and pathogenesis. Recurrent mutations in H3.3 and its chaperones have been identified in neoplastic transformation and developmental disorders, providing new insights into chromatin biology and disease. Here, we review recent findings emphasizing how two distinct histone chaperones, HIRA and DAXX, take part in the spatial and temporal distribution of H3.3 in different chromatin domains and ultimately achieve dynamic control of chromatin organization and function. Elucidating the H3.3 deposition pathways from the available histone pool will open new avenues for understanding the mechanisms by which H3.3 epigenetically regulates gene expression and its impact on cellular integrity and pathogenesis.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2092-6413
Relation: https://doaj.org/toc/2092-6413
DOI: 10.1038/s12276-023-01145-3
URL الوصول: https://doaj.org/article/df1c40ffb41e4497a46e15ac03e5348f
رقم الأكسشن: edsdoj.f1c40ffb41e4497a46e15ac03e5348f
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20926413
DOI:10.1038/s12276-023-01145-3