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HOXC9 directly regulates distinct sets of genes to coordinate diverse cellular processes during neuronal differentiation

BACKGROUND: Cellular differentiation is characterized by the acquisition of specialized structures and functions, cell cycle exit, and global attenuation of the DNA damage response. It is largely unknown how these diverse cellular events are coordinated at the molecular level during differentiation....

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Autores principales: Wang, Xiangwei, Choi, Jeong-Hyeon, Ding, Jane, Yang, Liqun, Ngoka, Lambert C, Lee, Eun J, Zha, Yunhong, Mao, Ling, Jin, Bilian, Ren, Mingqiang, Cowell, John, Huang, Shuang, Shi, Huidong, Cui, Hongjuan, Ding, Han-Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906982/
https://www.ncbi.nlm.nih.gov/pubmed/24274069
http://dx.doi.org/10.1186/1471-2164-14-830
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author Wang, Xiangwei
Choi, Jeong-Hyeon
Ding, Jane
Yang, Liqun
Ngoka, Lambert C
Lee, Eun J
Zha, Yunhong
Mao, Ling
Jin, Bilian
Ren, Mingqiang
Cowell, John
Huang, Shuang
Shi, Huidong
Cui, Hongjuan
Ding, Han-Fei
author_facet Wang, Xiangwei
Choi, Jeong-Hyeon
Ding, Jane
Yang, Liqun
Ngoka, Lambert C
Lee, Eun J
Zha, Yunhong
Mao, Ling
Jin, Bilian
Ren, Mingqiang
Cowell, John
Huang, Shuang
Shi, Huidong
Cui, Hongjuan
Ding, Han-Fei
author_sort Wang, Xiangwei
collection PubMed
description BACKGROUND: Cellular differentiation is characterized by the acquisition of specialized structures and functions, cell cycle exit, and global attenuation of the DNA damage response. It is largely unknown how these diverse cellular events are coordinated at the molecular level during differentiation. We addressed this question in a model system of neuroblastoma cell differentiation induced by HOXC9. RESULTS: We conducted a genome-wide analysis of the HOXC9-induced neuronal differentiation program. Microarray gene expression profiling revealed that HOXC9-induced differentiation was associated with transcriptional regulation of 2,370 genes, characterized by global upregulation of neuronal genes and downregulation of cell cycle and DNA repair genes. Remarkably, genome-wide mapping by ChIP-seq demonstrated that HOXC9 bound to 40% of these genes, including a large number of genes involved in neuronal differentiation, cell cycle progression and the DNA damage response. Moreover, we showed that HOXC9 interacted with the transcriptional repressor E2F6 and recruited it to the promoters of cell cycle genes for repressing their expression. CONCLUSIONS: Our results demonstrate that HOXC9 coordinates diverse cellular processes associated with differentiation by directly activating and repressing the transcription of distinct sets of genes.
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spelling pubmed-39069822014-01-31 HOXC9 directly regulates distinct sets of genes to coordinate diverse cellular processes during neuronal differentiation Wang, Xiangwei Choi, Jeong-Hyeon Ding, Jane Yang, Liqun Ngoka, Lambert C Lee, Eun J Zha, Yunhong Mao, Ling Jin, Bilian Ren, Mingqiang Cowell, John Huang, Shuang Shi, Huidong Cui, Hongjuan Ding, Han-Fei BMC Genomics Research Article BACKGROUND: Cellular differentiation is characterized by the acquisition of specialized structures and functions, cell cycle exit, and global attenuation of the DNA damage response. It is largely unknown how these diverse cellular events are coordinated at the molecular level during differentiation. We addressed this question in a model system of neuroblastoma cell differentiation induced by HOXC9. RESULTS: We conducted a genome-wide analysis of the HOXC9-induced neuronal differentiation program. Microarray gene expression profiling revealed that HOXC9-induced differentiation was associated with transcriptional regulation of 2,370 genes, characterized by global upregulation of neuronal genes and downregulation of cell cycle and DNA repair genes. Remarkably, genome-wide mapping by ChIP-seq demonstrated that HOXC9 bound to 40% of these genes, including a large number of genes involved in neuronal differentiation, cell cycle progression and the DNA damage response. Moreover, we showed that HOXC9 interacted with the transcriptional repressor E2F6 and recruited it to the promoters of cell cycle genes for repressing their expression. CONCLUSIONS: Our results demonstrate that HOXC9 coordinates diverse cellular processes associated with differentiation by directly activating and repressing the transcription of distinct sets of genes. BioMed Central 2013-11-25 /pmc/articles/PMC3906982/ /pubmed/24274069 http://dx.doi.org/10.1186/1471-2164-14-830 Text en Copyright © 2013 Wang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Xiangwei
Choi, Jeong-Hyeon
Ding, Jane
Yang, Liqun
Ngoka, Lambert C
Lee, Eun J
Zha, Yunhong
Mao, Ling
Jin, Bilian
Ren, Mingqiang
Cowell, John
Huang, Shuang
Shi, Huidong
Cui, Hongjuan
Ding, Han-Fei
HOXC9 directly regulates distinct sets of genes to coordinate diverse cellular processes during neuronal differentiation
title HOXC9 directly regulates distinct sets of genes to coordinate diverse cellular processes during neuronal differentiation
title_full HOXC9 directly regulates distinct sets of genes to coordinate diverse cellular processes during neuronal differentiation
title_fullStr HOXC9 directly regulates distinct sets of genes to coordinate diverse cellular processes during neuronal differentiation
title_full_unstemmed HOXC9 directly regulates distinct sets of genes to coordinate diverse cellular processes during neuronal differentiation
title_short HOXC9 directly regulates distinct sets of genes to coordinate diverse cellular processes during neuronal differentiation
title_sort hoxc9 directly regulates distinct sets of genes to coordinate diverse cellular processes during neuronal differentiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906982/
https://www.ncbi.nlm.nih.gov/pubmed/24274069
http://dx.doi.org/10.1186/1471-2164-14-830
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