XB-ART-54394Biochem Biophys Res Commun January 15, 2018; 495 (3): 2257-2263.
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Anosmin-1 is essential for neural crest and cranial placodes formation in Xenopus.
During embryogenesis vertebrates develop a complex craniofacial skeleton associated with sensory organs. These structures are primarily derived from two embryonic cell populations the neural crest and cranial placodes, respectively. Neural crest cells and cranial placodes are specified through the integrated action of several families of signaling molecules, and the subsequent activation of a complex network of transcription factors. Here we describe the expression and function of Anosmin-1 (Anos1), an extracellular matrix protein, during neural crest and cranial placodes development in Xenopus laevis. Anos1 was identified as a target of Pax3 and Zic1, two transcription factors necessary and sufficient to generate neural crest and cranial placodes. Anos1 is expressed in cranial neural crest progenitors at early neurula stage and in cranial placode derivatives later in development. We show that Anos1 function is required for neural crest and sensory organs development in Xenopus, consistent with the defects observed in Kallmann syndrome patients carrying a mutation in ANOS1. These findings indicate that anos1 has a conserved function in the development of craniofacial structures, and indicate that anos1-depleted Xenopus embryos represent a useful model to analyze the pathogenesis of Kallmann syndrome.
PubMed ID: 29277616
PMC ID: PMC6193491
Article link: Biochem Biophys Res Commun
Species referenced: Xenopus laevis
Genes referenced: anos1 dmrta1 ebf2 emx2 foxe1 foxe3 foxi4.1 foxi4.2 myc nog odc1 pax3 pax8 six1 snai2 sox10 sox2 sox8 wnt8a zic1
GO keywords: sensory organ development
Morpholinos: anos1 MO1 pax3 MO1 zic1 MO1
Disease Ontology terms: Kallmann syndrome
OMIMs: HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1
Article Images: [+] show captions
|Fig. 1. Developmental expression of anos1 by whole-mount ISH. (A–C) At the neurula stage (NF stage 14–17), anos1 is detected in the prospective neural crest territory (white arrowheads). (D–F) At stage 23, anos1 is now more broadly expressed, to include the somites (green arrowheads), otic vesicle (red arrowhead), the anterior pituitary (yellow arrowhead) in addition to the branchial arches (white arrowheads). (G–H) Later in development (NF stage 27) anos1 persists in all these tissues. (A–C) dorsal views, anterior to top. (D, G) lateral views, dorsal to top, anterior to left. (E, F, H) frontal views, dorsal to top. The embryonic stages (NF) are indicated in the lower right corner of each panel. (I) Relative expression levels of anos1 and snail2 analyzed by qRT-PCR at the indicated stages. The values were normalized to odc1. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)|
|Fig. 2. anos1 is a target of Pax3 and Zic1. (A) Injection of pax3MO (40 ng) or zic1MO (40 ng) reduces anos1 expression at the neurula stage. Dorsal views, anterior to top. The injected side is to the right as indicated by the presence of the lineage tracer (Red-Gal). The graph indicates the percentage of embryos with normal (white) or reduced/lost (red) anos1 expression. The number of embryos analyzed is indicated on top of each bar. (B) mRNA encoding pax3GR and zic1GR (100 pg each), alone or in combination were injected into both blastomeres in the animal pole at the 2-cell stage. At the blastula stage (stage 9), animal cap (AC) explants were dissected and cultured for 8 h in the presence of dexamethasone (+dex). (C) anos1 and snai2 expression in pax3GR and zic1GR injected AC explants analyzed by qRT-PCR.|
|Fig. 3. Anos1 is required for neural crest formation. (A) Western blot of embryos injected with mRNA encoding a myc-tagged version of Xenopus anos1, alone or in combination with increasing doses of anos1MO, 10 ng (+), 20 ng (++), and 40 ng (+++), showed that anos1MO blocks Anos1 protein accumulation. (B) Unilateral injection of anos1MO (40 ng) at the 2-cell stage causes a reduction/loss of expression of snail2 and sox10, and a lateral expansion of sox2 expression domain. Injection of Xenopus anos1 mRNAs (3 ng) did not significantly affect snail2 and sox10 expression levels, although their expression domain was shifted laterally. The expression of sox2 was only marginally expanded in these embryos. Dorsal views, anterior to top. The injected side is to the right (Red-Gal). (C) The graphs indicate the percentage of embryos with normal (white), reduced/lost (red) expression. The number of embryos analyzed is indicated on top of each bar. (D) In explants, the induction of snail2 and sox8 by co-injection of noggin (200 pg) and wnt8a (10 pg) mRNA is dramatically reduced in the context of embryos injected with anos1MO (40 ng). This reduction in neural crest genes expression is associated by an increase in sox2 expression. The values were normalized to ef1α. A representative experiments is shown from three independent experiments. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)|
|Fig. 4. Anos1 is essential for the formation of cranial placodes and their derivatives. (A–D) Unilateral injection of anos1MO (40 ng) at the 2-cell stage causes a reduction/loss of expression of two pan-placodal genes, six1 (A) and foxi4.1 (B), as well as genes restricted to individual placodal domains such as dmrta1 (C) and pax8 (D). (E–G) Later in development, the injected embryos exhibited reduce dmrta1 (E), emx2 (F) and ebf2 (G) expression in the olfactory epithelium. (H–I) The expression of foxe1 in the developing pituitary was also reduced (I) as compared to sibling control (H). (A–I) Anterior views, dorsal to top. The injected side (arrowheads) is to the right. The percentage of affected embryos is indicated in the upper right corner of each panel.|
References [+] :
Aoki, Sox10 regulates the development of neural crest-derived melanocytes in Xenopus. 2003, Pubmed, Xenbase