PUBLICATION

A missense mutation in zbtb17 blocks the earliest steps of T cell differentiation in zebrafish

Authors
Lawir, D.F., Iwanami, N., Schorpp, M., Boehm, T.
ID
ZDB-PUB-170308-8
Date
2017
Source
Scientific Reports   7: 44145 (Journal)
Registered Authors
Boehm, Tom, Schorpp, Michael
Keywords
Haematopoiesis, Immunology, Lymphopoiesis
MeSH Terms
  • Animals
  • Cell Differentiation*/genetics
  • Cell Differentiation*/immunology
  • Mutation, Missense*
  • T-Lymphocytes/cytology
  • T-Lymphocytes/immunology*
  • Transcription Factors*/genetics
  • Transcription Factors*/immunology
  • Zebrafish*/genetics
  • Zebrafish*/immunology
  • Zebrafish Proteins*/genetics
  • Zebrafish Proteins*/immunology
PubMed
28266617 Full text @ Sci. Rep.
Abstract
T cells are an evolutionarily conserved feature of the adaptive immune systems of vertebrates. Comparative studies using evolutionarily distant species hold great promise for unraveling the genetic landscape underlying this process. To this end, we used ENU mutagenesis to generate mutant zebrafish with specific aberrations in early T cell development. Here, we describe the identification of a recessive missense mutation in the transcriptional regulator zbtb17 (Q562K), which affects the ninth zinc finger module of the protein. Homozygous mutant fish exhibit an early block of intrathymic T cell development, as a result of impaired thymus colonization owing to reduced expression of the gene encoding the homing receptor ccr9a, and inefficient T cell differentiation owing to reduced expression of socs1a. Our results reveal the zbtb17-socs1 axis as an evolutionarily conserved central regulatory module of early T cell development of vertebrates.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping