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Stage-specific and cell type-specific requirements of ikzf1 during haematopoietic differentiation in zebrafish
被引:6
作者:

Hess, Isabell
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Immunobiol & Epigenet, Dept Dev Immunol, Stuebeweg 51, D-79108 Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Dept Dev Immunol, Stuebeweg 51, D-79108 Freiburg, Germany

Sagar
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Immunobiol & Epigenet, Quantitat Single Cell Biol Grp, Stuebeweg 51, D-79108 Freiburg, Germany
Univ Hosp Freiburg, Dept Med 2, Hugstetter Str 55, D-79106 Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Dept Dev Immunol, Stuebeweg 51, D-79108 Freiburg, Germany

O'Meara, Connor
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h-index: 0
机构:
Max Planck Inst Immunobiol & Epigenet, Dept Dev Immunol, Stuebeweg 51, D-79108 Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Dept Dev Immunol, Stuebeweg 51, D-79108 Freiburg, Germany

Gruen, Dominic
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h-index: 0
机构:
Max Planck Inst Immunobiol & Epigenet, Quantitat Single Cell Biol Grp, Stuebeweg 51, D-79108 Freiburg, Germany
Julius Maximilians Univ Wurzburg, Max Planck Res Grp, Wurzburg Inst Syst Immunol, Versbacher Str 9, D-97078 Wurzburg, Germany
Helmholtz Ctr Infect Res HZI, Helmholtz Inst RNA Based Infect Res HIRI, Josef Schneider Str 2, D-97080 Wurzburg, Germany Max Planck Inst Immunobiol & Epigenet, Dept Dev Immunol, Stuebeweg 51, D-79108 Freiburg, Germany

Schorpp, Michael
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Immunobiol & Epigenet, Dept Dev Immunol, Stuebeweg 51, D-79108 Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Dept Dev Immunol, Stuebeweg 51, D-79108 Freiburg, Germany

Boehm, Thomas
论文数: 0 引用数: 0
h-index: 0
机构:
Max Planck Inst Immunobiol & Epigenet, Dept Dev Immunol, Stuebeweg 51, D-79108 Freiburg, Germany
Univ Freiburg, Fac Med, Breisacher Str 153, D-79110 Freiburg, Germany Max Planck Inst Immunobiol & Epigenet, Dept Dev Immunol, Stuebeweg 51, D-79108 Freiburg, Germany
机构:
[1] Max Planck Inst Immunobiol & Epigenet, Dept Dev Immunol, Stuebeweg 51, D-79108 Freiburg, Germany
[2] Max Planck Inst Immunobiol & Epigenet, Quantitat Single Cell Biol Grp, Stuebeweg 51, D-79108 Freiburg, Germany
[3] Univ Hosp Freiburg, Dept Med 2, Hugstetter Str 55, D-79106 Freiburg, Germany
[4] Julius Maximilians Univ Wurzburg, Max Planck Res Grp, Wurzburg Inst Syst Immunol, Versbacher Str 9, D-97078 Wurzburg, Germany
[5] Helmholtz Ctr Infect Res HZI, Helmholtz Inst RNA Based Infect Res HIRI, Josef Schneider Str 2, D-97080 Wurzburg, Germany
[6] Univ Freiburg, Fac Med, Breisacher Str 153, D-79110 Freiburg, Germany
基金:
欧洲研究理事会;
关键词:
TEMPORAL IDENTITY;
GENETIC-EVIDENCE;
IKAROS FAMILY;
EXPRESSION;
TRANSPLANTATION;
PROGENITORS;
MOUSE;
D O I:
10.1038/s41598-022-25978-6
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
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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