http://www.cnr.it/ontology/cnr/individuo/prodotto/ID26906
Selective inactivation of Otx2 mRNA isoforms reveals isoform-specific requirement for visceral endoderm anteriorization and head morphogenesis and highlights cell diversity in the visceral endoderm (Articolo in rivista)
- Type
- Label
- Selective inactivation of Otx2 mRNA isoforms reveals isoform-specific requirement for visceral endoderm anteriorization and head morphogenesis and highlights cell diversity in the visceral endoderm (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.mod.2009.07.003 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Acampora D.; Di Giovannantonio L.G.; Di Salvio M.; Mancuso P.; Simeone A. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#note
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- CEINGE Biotecnologie Avanzate, Via Comunale Margherita 482, 80145 Naples, Italy
SEMM European School of Molecular Medicine - Naples Site, Italy
Institute of Genetics and Biophysics ''A. Buzzati-Traverso'', CNR, Via P. Castellino 111, 80131 Naples, Italy (literal)
- Titolo
- Selective inactivation of Otx2 mRNA isoforms reveals isoform-specific requirement for visceral endoderm anteriorization and head morphogenesis and highlights cell diversity in the visceral endoderm (literal)
- Abstract
- Genetic and embryological experiments demonstrated that the visceral endoderm (VE) is
essential for positioning the primitive streak at one pole of the embryo and head morphogenesis
through antagonism of the Wnt and Nodal signaling pathways. The transcription
factor Otx2 is required for VE anteriorization and specification of rostral neuroectoderm
at least in part by controlling the expression of Dkk1 and Lefty1. Here, we investigated
the relevance of the Otx2 transcriptional control in these processes. Otx2 protein is encoded
by different mRNAs variants, which, on the basis of their transcription start site, may be
distinguished in distal and proximal. Distal isoforms are prevalently expressed in the epiblast
and neuroectoderm, while proximal isoforms prevalently in the VE. Selective inactivation
of Otx2 variants reveals that distal isoforms are not required for gastrulation, but
essential for maintenance of forebrain and midbrain identities; conversely, proximal isoforms
control VE anteriorization and, indirectly, primitive streak positioning through the
activation of Dkk1 and Lefty1. Moreover, in these mutants the expression of proximal isoforms
is not affected by the lack of distal mRNAs and vice versa. Taken together these findings
indicate that proximal and distal isoforms, whose expression is independently
regulated in the VE and epiblast-derived neuroectoderm, functionally cooperate to provide
these tissues with the sufficient level of Otx2 necessary to promote a normal development.
Furthermore, we discovered that in the VE the expression of Otx2 isoforms is tightly controlled
at single cell level, and we hypothesize that this molecular diversity may potentially
confer specific functional properties to different subsets of VE cells (literal)
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