Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/81119
Title: Remodeling of nuclear landscapes during human myelopoietic cell differentiation maintains co-aligned active and inactive nuclear compartments
Authors: Markaki, Yolanda
Ferrari, Sergio
Cremer, Marion
Hübner, Barbara
Lomiento, Mariana
Mammoli, Fabiana
Illner, Doris
Cremer, Thomas
Keywords: Myelopoiesis
Somatic cell differentiation
Nuclear architecture
Active nuclear compartment
Interchromatin compartment
Perichromatin region
Super-resolution microscopy
Electron microscopy
Chromatin domain
Chromatin density classification
Issue Date: 2015
Source: Hübner, B., Lomiento, M., Mammoli, F., Illner, D., Markaki, Y., Ferrari, S., et al. (2015). Remodeling of nuclear landscapes during human myelopoietic cell differentiation maintains co-aligned active and inactive nuclear compartments. Epigenetics & Chromatin, 8, 47-.
Series/Report no.: Epigenetics & Chromatin
Abstract: Background: Previous studies of higher order chromatin organization in nuclei of mammalian species revealed both structural consistency and species-specific differences between cell lines and during early embryonic development. Here, we extended our studies to nuclear landscapes in the human myelopoietic lineage representing a somatic cell differentiation system. Our longterm goal is a search for structural features of nuclei, which are restricted to certain cell types/species, as compared to features, which are evolutionary highly conserved, arguing for their basic functional roles in nuclear organization. Results: Common human hematopoietic progenitors, myeloid precursor cells, differentiated monocytes and granulocytes analyzed by super-resolution fluorescence microscopy and electron microscopy revealed profound differences with respect to global chromatin arrangements, the nuclear space occupied by the interchromatin compartment and the distribution of nuclear pores. In contrast, we noted a consistent organization in all cell types with regard to two co-aligned networks, an active (ANC) and an inactive (INC) nuclear compartment delineated by functionally relevant hallmarks. The ANC is enriched in active RNA polymerase II, splicing speckles and histone signatures for transcriptionally competent chromatin (H3K4me3), whereas the INC carries marks for repressed chromatin (H3K9me3). Conclusions: Our findings substantiate the conservation of the recently published ANC-INC network model of mammalian nuclear organization during human myelopoiesis irrespective of profound changes of the global nuclear architecture observed during this differentiation process. According to this model, two spatially co-aligned and functionally interacting active and inactive nuclear compartments (ANC and INC) pervade the nuclear space.
URI: https://hdl.handle.net/10356/81119
http://hdl.handle.net/10220/39099
ISSN: 1756-8935
DOI: 10.1186/s13072-015-0038-0
Schools: School of Biological Sciences 
Rights: © 2015 Hübner et al. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SBS Journal Articles

SCOPUSTM   
Citations 20

30
Updated on Jun 14, 2024

Web of ScienceTM
Citations 10

33
Updated on Oct 29, 2023

Page view(s)

372
Updated on Jun 18, 2024

Download(s) 10

389
Updated on Jun 18, 2024

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.