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The histone chaperone Nrp1 is required for chromatin stability and nuclear division in Tetrahymena thermophila
Histone chaperones facilitate DNA replication and repair by promoting chromatin assembly, disassembly and histone exchange. Following histones synthesis and nucleosome assembly, the histones undergo posttranslational modification by different enzymes and are deposited onto chromatins by various hist...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299592/ https://www.ncbi.nlm.nih.gov/pubmed/34301312 http://dx.doi.org/10.1186/s13072-021-00409-4 |
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author | Lian, Yinjie Hao, Huijuan Xu, Jing Bo, Tao Liang, Aihua Wang, Wei |
author_facet | Lian, Yinjie Hao, Huijuan Xu, Jing Bo, Tao Liang, Aihua Wang, Wei |
author_sort | Lian, Yinjie |
collection | PubMed |
description | Histone chaperones facilitate DNA replication and repair by promoting chromatin assembly, disassembly and histone exchange. Following histones synthesis and nucleosome assembly, the histones undergo posttranslational modification by different enzymes and are deposited onto chromatins by various histone chaperones. In Tetrahymena thermophila, histones from macronucleus (MAC) and micronucleus (MIC) have been comprehensively investigated, but the function of histone chaperones remains unclear. Histone chaperone Nrp1 in Tetrahymena contains four conserved tetratricopepeptide repeat (TPR) domains and one C-terminal nuclear localization signal. TPR2 is typically interrupted by a large acidic motif. Immunofluorescence staining showed that Nrp1 is located in the MAC and MICs, but disappeared in the apoptotic parental MAC and the degraded MICs during the conjugation stage. Nrp1 was also colocalized with α-tubulin around the spindle structure. NRP1 knockdown inhibited cellular proliferation and led to the loss of chromosome, abnormal macronuclear amitosis, and disorganized micronuclear mitosis during the vegetative growth stage. During sexual developmental stage, the gametic nuclei failed to be selected and abnormally degraded in NRP1 knockdown mutants. Affinity purification combined with mass spectrometry analysis indicated that Nrp1 is co-purified with core histones, heat shock proteins, histone chaperones, and DNA damage repair proteins. The physical direct interaction of Nrp1 and Asf1 was also confirmed by pull-down analysis in vitro. The results show that histone chaperone Nrp1 is involved in micronuclear mitosis and macronuclear amitosis in the vegetative growth stage and maintains gametic nuclei formation during the sexual developmental stage. Nrp1 is required for chromatin stability and nuclear division in Tetrahymena thermophila. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13072-021-00409-4. |
format | Online Article Text |
id | pubmed-8299592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82995922021-07-28 The histone chaperone Nrp1 is required for chromatin stability and nuclear division in Tetrahymena thermophila Lian, Yinjie Hao, Huijuan Xu, Jing Bo, Tao Liang, Aihua Wang, Wei Epigenetics Chromatin Research Histone chaperones facilitate DNA replication and repair by promoting chromatin assembly, disassembly and histone exchange. Following histones synthesis and nucleosome assembly, the histones undergo posttranslational modification by different enzymes and are deposited onto chromatins by various histone chaperones. In Tetrahymena thermophila, histones from macronucleus (MAC) and micronucleus (MIC) have been comprehensively investigated, but the function of histone chaperones remains unclear. Histone chaperone Nrp1 in Tetrahymena contains four conserved tetratricopepeptide repeat (TPR) domains and one C-terminal nuclear localization signal. TPR2 is typically interrupted by a large acidic motif. Immunofluorescence staining showed that Nrp1 is located in the MAC and MICs, but disappeared in the apoptotic parental MAC and the degraded MICs during the conjugation stage. Nrp1 was also colocalized with α-tubulin around the spindle structure. NRP1 knockdown inhibited cellular proliferation and led to the loss of chromosome, abnormal macronuclear amitosis, and disorganized micronuclear mitosis during the vegetative growth stage. During sexual developmental stage, the gametic nuclei failed to be selected and abnormally degraded in NRP1 knockdown mutants. Affinity purification combined with mass spectrometry analysis indicated that Nrp1 is co-purified with core histones, heat shock proteins, histone chaperones, and DNA damage repair proteins. The physical direct interaction of Nrp1 and Asf1 was also confirmed by pull-down analysis in vitro. The results show that histone chaperone Nrp1 is involved in micronuclear mitosis and macronuclear amitosis in the vegetative growth stage and maintains gametic nuclei formation during the sexual developmental stage. Nrp1 is required for chromatin stability and nuclear division in Tetrahymena thermophila. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13072-021-00409-4. BioMed Central 2021-07-23 /pmc/articles/PMC8299592/ /pubmed/34301312 http://dx.doi.org/10.1186/s13072-021-00409-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Lian, Yinjie Hao, Huijuan Xu, Jing Bo, Tao Liang, Aihua Wang, Wei The histone chaperone Nrp1 is required for chromatin stability and nuclear division in Tetrahymena thermophila |
title | The histone chaperone Nrp1 is required for chromatin stability and nuclear division in Tetrahymena thermophila |
title_full | The histone chaperone Nrp1 is required for chromatin stability and nuclear division in Tetrahymena thermophila |
title_fullStr | The histone chaperone Nrp1 is required for chromatin stability and nuclear division in Tetrahymena thermophila |
title_full_unstemmed | The histone chaperone Nrp1 is required for chromatin stability and nuclear division in Tetrahymena thermophila |
title_short | The histone chaperone Nrp1 is required for chromatin stability and nuclear division in Tetrahymena thermophila |
title_sort | histone chaperone nrp1 is required for chromatin stability and nuclear division in tetrahymena thermophila |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299592/ https://www.ncbi.nlm.nih.gov/pubmed/34301312 http://dx.doi.org/10.1186/s13072-021-00409-4 |
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