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Stage-specific and cell type-specific requirements of ikzf1 during haematopoietic differentiation in zebrafish

The zinc finger transcription factor Ikaros1 (Ikzf1) is required for lymphoid development in mammals. Four zinc fingers constitute its DNA binding domain and two zinc fingers are present in the C-terminal protein interaction module. We describe the phenotypes of zebrafish homozygous for two distinct...

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Autores principales: Hess, Isabell, Sagar, O´Meara, Connor, Grün, Dominic, Schorpp, Michael, Boehm, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741631/
https://www.ncbi.nlm.nih.gov/pubmed/36496511
http://dx.doi.org/10.1038/s41598-022-25978-6
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author Hess, Isabell
Sagar
O´Meara, Connor
Grün, Dominic
Schorpp, Michael
Boehm, Thomas
author_facet Hess, Isabell
Sagar
O´Meara, Connor
Grün, Dominic
Schorpp, Michael
Boehm, Thomas
author_sort Hess, Isabell
collection PubMed
description The zinc finger transcription factor Ikaros1 (Ikzf1) is required for lymphoid development in mammals. Four zinc fingers constitute its DNA binding domain and two zinc fingers are present in the C-terminal protein interaction module. We describe the phenotypes of zebrafish homozygous for two distinct mutant ikzf1 alleles. The IT325 variant lacks the C-terminal two zinc fingers, whereas the fr105 variant retains only the first zinc finger of the DNA binding domain. An intact ikzf1 gene is required for larval T cell development, whereas low levels of adult lymphoid development recover in the mutants. By contrast, the mutants exhibit a signature of increased myelopoiesis at larval and adult stages. Both mutations stimulate erythroid differentiation in larvae, indicating that the C-terminal zinc fingers negatively regulate the extent of red blood cell production. An unexpected differential effect of the two mutants on adult erythropoiesis suggests a direct requirement of an intact DNA binding domain for entry of progenitors into the red blood cell lineage. Collectively, our results reinforce the biological differences between larval and adult haematopoiesis, indicate a stage-specific function of ikzf1 in regulating the hierarchical bifurcations of differentiation, and assign distinct functions to the DNA binding domain and the C-terminal zinc fingers.
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spelling pubmed-97416312022-12-12 Stage-specific and cell type-specific requirements of ikzf1 during haematopoietic differentiation in zebrafish Hess, Isabell Sagar O´Meara, Connor Grün, Dominic Schorpp, Michael Boehm, Thomas Sci Rep Article The zinc finger transcription factor Ikaros1 (Ikzf1) is required for lymphoid development in mammals. Four zinc fingers constitute its DNA binding domain and two zinc fingers are present in the C-terminal protein interaction module. We describe the phenotypes of zebrafish homozygous for two distinct mutant ikzf1 alleles. The IT325 variant lacks the C-terminal two zinc fingers, whereas the fr105 variant retains only the first zinc finger of the DNA binding domain. An intact ikzf1 gene is required for larval T cell development, whereas low levels of adult lymphoid development recover in the mutants. By contrast, the mutants exhibit a signature of increased myelopoiesis at larval and adult stages. Both mutations stimulate erythroid differentiation in larvae, indicating that the C-terminal zinc fingers negatively regulate the extent of red blood cell production. An unexpected differential effect of the two mutants on adult erythropoiesis suggests a direct requirement of an intact DNA binding domain for entry of progenitors into the red blood cell lineage. Collectively, our results reinforce the biological differences between larval and adult haematopoiesis, indicate a stage-specific function of ikzf1 in regulating the hierarchical bifurcations of differentiation, and assign distinct functions to the DNA binding domain and the C-terminal zinc fingers. Nature Publishing Group UK 2022-12-10 /pmc/articles/PMC9741631/ /pubmed/36496511 http://dx.doi.org/10.1038/s41598-022-25978-6 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 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/) .
spellingShingle Article
Hess, Isabell
Sagar
O´Meara, Connor
Grün, Dominic
Schorpp, Michael
Boehm, Thomas
Stage-specific and cell type-specific requirements of ikzf1 during haematopoietic differentiation in zebrafish
title Stage-specific and cell type-specific requirements of ikzf1 during haematopoietic differentiation in zebrafish
title_full Stage-specific and cell type-specific requirements of ikzf1 during haematopoietic differentiation in zebrafish
title_fullStr Stage-specific and cell type-specific requirements of ikzf1 during haematopoietic differentiation in zebrafish
title_full_unstemmed Stage-specific and cell type-specific requirements of ikzf1 during haematopoietic differentiation in zebrafish
title_short Stage-specific and cell type-specific requirements of ikzf1 during haematopoietic differentiation in zebrafish
title_sort stage-specific and cell type-specific requirements of ikzf1 during haematopoietic differentiation in zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741631/
https://www.ncbi.nlm.nih.gov/pubmed/36496511
http://dx.doi.org/10.1038/s41598-022-25978-6
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