Maternal pak4 expression is required for primitive myelopoiesis in zebrafish

► Zebrafish pak4 is required for primitive myeloid cell development. ► Maternal but not zygotic expression is required. ► Early patterning signals are not affected. ► Spatial patterning of hematopoietic domains is not affected. ► The pak4 loss of function can be mimicked by treatment with actin depo...

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Veröffentlicht in:Mechanisms of development 2013-02, Vol.130 (2-3), p.181-194
Hauptverfasser: Law, Sheran H.W., Sargent, Thomas D.
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Sprache:eng
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Zusammenfassung:► Zebrafish pak4 is required for primitive myeloid cell development. ► Maternal but not zygotic expression is required. ► Early patterning signals are not affected. ► Spatial patterning of hematopoietic domains is not affected. ► The pak4 loss of function can be mimicked by treatment with actin depolymerization drugs. Transcripts of pak4, the zebrafish ortholog of p21-activated kinase 4 (PAK4), are most abundant in the egg and fall to low levels by the end of gastrulation, after which expression is essentially ubiquitous. Translation of maternal mRNA into pak4 protein is first detectable at high stage (3.3hpf). Splice-blocking morpholino oligonucleotides (MOs) were used to prevent zygotic pak4 expression. This had no discernable effect on development through larval stages. In contrast, a translation-blocking MO, alone or in combination with the splice MOs, resulted in a complex lethal phenotype. In addition to disrupted somite development and other morphogenetic abnormalities, the knockdown of maternal pak4 expression led to alterations in regulatory gene expression in the primitive hematopoietic domains, leading to deficiencies in granulocyte and leukocyte lineages. At least some of the effects of pak4 knockdown on gene expression could be mimicked by treatment with actin depolymerization agents, suggesting a mechanistic link between regulation of microfilament dynamics by pak4 and regulation of gene expression in primitive myeloid cell differentiation.
ISSN:0925-4773
1872-6356
DOI:10.1016/j.mod.2012.09.005