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A Myb enhancer-guided analysis of basophil and mast cell differentiation
The transcription factor MYB is a crucial regulator of hematopoietic stem and progenitor cells. However, the nature of lineage-specific enhancer usage of the Myb gene is largely unknown. We identify the Myb −68 enhancer, a regulatory element which marks basophils and mast cells. Using the Myb −68 en...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9674656/ https://www.ncbi.nlm.nih.gov/pubmed/36400777 http://dx.doi.org/10.1038/s41467-022-34906-1 |
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author | Matsumura, Takayoshi Totani, Haruhito Gunji, Yoshitaka Fukuda, Masahiro Yokomori, Rui Deng, Jianwen Rethnam, Malini Yang, Chong Tan, Tze King Karasawa, Tadayoshi Kario, Kazuomi Takahashi, Masafumi Osato, Motomi Sanda, Takaomi Suda, Toshio |
author_facet | Matsumura, Takayoshi Totani, Haruhito Gunji, Yoshitaka Fukuda, Masahiro Yokomori, Rui Deng, Jianwen Rethnam, Malini Yang, Chong Tan, Tze King Karasawa, Tadayoshi Kario, Kazuomi Takahashi, Masafumi Osato, Motomi Sanda, Takaomi Suda, Toshio |
author_sort | Matsumura, Takayoshi |
collection | PubMed |
description | The transcription factor MYB is a crucial regulator of hematopoietic stem and progenitor cells. However, the nature of lineage-specific enhancer usage of the Myb gene is largely unknown. We identify the Myb −68 enhancer, a regulatory element which marks basophils and mast cells. Using the Myb −68 enhancer activity, we show a population of granulocyte-macrophage progenitors with higher potential to differentiate into basophils and mast cells. Single cell RNA-seq demonstrates the differentiation trajectory is continuous from progenitors to mature basophils in vivo, characterizes bone marrow cells with a gene signature of mast cells, and identifies LILRB4 as a surface marker of basophil maturation. Together, our study leads to a better understanding of how MYB expression is regulated in a lineage-associated manner, and also shows how a combination of lineage-related reporter mice and single-cell transcriptomics can overcome the rarity of target cells and enhance our understanding of gene expression programs that control cell differentiation in vivo. |
format | Online Article Text |
id | pubmed-9674656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96746562022-11-20 A Myb enhancer-guided analysis of basophil and mast cell differentiation Matsumura, Takayoshi Totani, Haruhito Gunji, Yoshitaka Fukuda, Masahiro Yokomori, Rui Deng, Jianwen Rethnam, Malini Yang, Chong Tan, Tze King Karasawa, Tadayoshi Kario, Kazuomi Takahashi, Masafumi Osato, Motomi Sanda, Takaomi Suda, Toshio Nat Commun Article The transcription factor MYB is a crucial regulator of hematopoietic stem and progenitor cells. However, the nature of lineage-specific enhancer usage of the Myb gene is largely unknown. We identify the Myb −68 enhancer, a regulatory element which marks basophils and mast cells. Using the Myb −68 enhancer activity, we show a population of granulocyte-macrophage progenitors with higher potential to differentiate into basophils and mast cells. Single cell RNA-seq demonstrates the differentiation trajectory is continuous from progenitors to mature basophils in vivo, characterizes bone marrow cells with a gene signature of mast cells, and identifies LILRB4 as a surface marker of basophil maturation. Together, our study leads to a better understanding of how MYB expression is regulated in a lineage-associated manner, and also shows how a combination of lineage-related reporter mice and single-cell transcriptomics can overcome the rarity of target cells and enhance our understanding of gene expression programs that control cell differentiation in vivo. Nature Publishing Group UK 2022-11-18 /pmc/articles/PMC9674656/ /pubmed/36400777 http://dx.doi.org/10.1038/s41467-022-34906-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Matsumura, Takayoshi Totani, Haruhito Gunji, Yoshitaka Fukuda, Masahiro Yokomori, Rui Deng, Jianwen Rethnam, Malini Yang, Chong Tan, Tze King Karasawa, Tadayoshi Kario, Kazuomi Takahashi, Masafumi Osato, Motomi Sanda, Takaomi Suda, Toshio A Myb enhancer-guided analysis of basophil and mast cell differentiation |
title | A Myb enhancer-guided analysis of basophil and mast cell differentiation |
title_full | A Myb enhancer-guided analysis of basophil and mast cell differentiation |
title_fullStr | A Myb enhancer-guided analysis of basophil and mast cell differentiation |
title_full_unstemmed | A Myb enhancer-guided analysis of basophil and mast cell differentiation |
title_short | A Myb enhancer-guided analysis of basophil and mast cell differentiation |
title_sort | myb enhancer-guided analysis of basophil and mast cell differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9674656/ https://www.ncbi.nlm.nih.gov/pubmed/36400777 http://dx.doi.org/10.1038/s41467-022-34906-1 |
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