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Human Molecular Genetics, 2000, Vol. 9, No. 9 1443-1452
© 2000 Oxford University Press

Barhl1, a gene belonging to a new subfamily of mammalian homeobox genes, is expressed in migrating neurons of the CNS

Alessandro Bulfone1,+, Emilio Menguzzato1,+, Vania Broccoli1, Anna Marchitiello1, Claudio Gattuso1, Margherita Mariani2, Gian Giacomo Consalez2, Salvador Martinez4, Andrea Ballabio1,3 and Sandro Banfi1

1Telethon Institute of Genetics and Medicine (TIGEM), 2Department of Biological and Technological Research (DIBIT), 3Universita’ Vita-Salute San Raffaele, San Raffaele Biomedical Science Park, Via Olgettina 58, 20132 Milan, Italy and 4Department of Morphological Sciences, Faculty of Medicine, University of Murcia, Murcia, Spain

The BarH1 and BarH2 (Bar) Drosophila genes are homeobox-containing genes, which are required for the fate determination of external sensory organs in the fly. By means of a bioinformatic approach, we have identified in mouse and human two homeobox genes highly related to the Bar Drosophila genes, Barhl1 and Barhl2. While Barhl1 represents a novel gene, Barhl2 turned out to correspond to the mBH1 cDNA recently described in rat. We isolated and sequenced the full-length mouse Barhl1 and mapped both the human BARHL1 and BARHL2 genes to chromosomes 9q34 and 1p22, respectively. Detailed analysis of the murine Barhl1 expression pattern by in situ hybridization revealed that this transcript is exclusively expressed in restricted domains of the developing CNS, which suggests that this gene, similar to its Drosophila counterparts BarH1 and BarH2, may play a crucial role in cell fate determin­ation of neural structures. In particular, Barhl1 showed specific domains of expression in the diencephalon and in the rhombencephalon where it was found to be expressed in migrating cells giving rise to the cerebellar external granular layer and to specific populations of dorsal sensory interneurons of the spinal cord. Thus, Barhl1 function may be required for the generation of these specific subtypes of neuronal progenitors. Furthermore, the mapping assignment and the expression pattern make BARHL1 an attractive positional candidate gene for a form of Joubert syndrome, a rare developmental anomaly of the cerebellum in humans.

+ These authors contributed equally to this work

§ Present address: Telethon Institute of Gene Therapy (TIGET), San Raffaele Biomedical Science Park, Milan, Italy

To whom correspondence should be addressed. Tel: +39 02 215601; Fax: +39 02 21560220; Email: banfi@tigem.it


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