Basonuclin 2 has a function in the multiplication of embryonic craniofacial mesenchymal cells and is orthologous to disco proteins

Autor: Fabrice Daubigney, Masatake Araki, Anna Maciejewski-Duval, Ken Ichi Yamamura, Guillaume Soubigou, Cyril Bouche, Amandine Vanhoutteghem, Françoise Hervé, Philippe Djian, Brigitte Delhomme, Kimi Araki
Přispěvatelé: Régulation de la transcription et maladies génétiques (RTMG), Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)
Rok vydání: 2009
Předmět:
Male
Mammalian embryology
Biology
DNA-binding protein
Cell Line
Craniofacial Abnormalities
03 medical and health sciences
Mice
0302 clinical medicine
Tongue
Animals
Drosophila Proteins
[SDV.BBM]Life Sciences [q-bio]/Biochemistry
Molecular Biology

RNA
Messenger

Fluorescent Antibody Technique
Indirect

Peptide sequence
Gene
030304 developmental biology
Cell Proliferation
Oligonucleotide Array Sequence Analysis
Genetics
Zinc finger
Regulation of gene expression
Mice
Knockout

0303 health sciences
Multidisciplinary
Reverse Transcriptase Polymerase Chain Reaction
Skull
Gene Expression Regulation
Developmental

Mesenchymal Stem Cells
Zinc Fingers
Biological Sciences
Blotting
Northern

Embryo
Mammalian

Embryonic stem cell
Cleft Palate
DNA-Binding Proteins
Animals
Newborn

Female
human activities
030217 neurology & neurosurgery
Drosophila Protein
Transcription Factors
Zdroj: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2009, 106 (34), pp.14432-7. ⟨10.1073/pnas.0905840106⟩
ISSN: 1091-6490
0027-8424
DOI: 10.1073/pnas.0905840106⟩
Popis: Basonuclin 2 is a recently discovered zinc finger protein of unknown function. Its paralog, basonuclin 1, is associated with the ability of keratinocytes to multiply. The basonuclin zinc fingers are closely related to those of the Drosophila proteins disco and discorelated, but the relation between disco proteins and basonuclins has remained elusive because the function of the disco proteins in larval head development seems to have no relation to that of basonuclin 1 and because the amino acid sequence of disco, apart from the zinc fingers, also has no similarity to that of the basonuclins. We have generated mice lacking basonuclin 2. These mice die within 24 h of birth with a cleft palate and abnormalities of craniofacial bones and tongue. In the embryonic head, expression of the basonuclin 2 gene is restricted to mesenchymal cells in the palate, at the periphery of the tongue, and in the mesenchymal sheaths that surround the brain and the osteocartilagineous structures. In late embryos, the rate of multiplication of these mesenchymal cells is greatly diminished. Therefore, basonuclin 2 is essential for the multiplication of craniofacial mesenchymal cells during embryogenesis. Non- Drosophila insect databases available since 2008 reveal that the basonuclins and the disco proteins share much more extensive sequence and gene structure similarity than noted when only Drosophila sequences were examined. We conclude that basonuclin 2 is both structurally and functionally the vertebrate ortholog of the disco proteins. We also note the possibility that some human craniofacial abnormalities are due to a lack of basonuclin 2.
Databáze: OpenAIRE