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
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
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
Y. Zhu, T. Matsumoto, S. Mikami, T. Nagasawa, and F. Murakami SDF1/CXCR4 signalling regulates two distinct processes of precerebellar neuronal migration and its depletion leads to abnormal pontine nuclei formation Development, June 1, 2009; 136(11): 1919 - 1928. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Liu, H. Li, X. Hu, L. Yu, H. Liu, R. Han, R. Colella, G. D. Mower, Y. Chen, and M. Qiu Control of Precerebellar Neuron Development by Olig3 bHLH Transcription Factor J. Neurosci., October 1, 2008; 28(40): 10124 - 10133. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Chellappa, S. Li, S. Pauley, I. Jahan, K. Jin, and M. Xiang Barhl1 Regulatory Sequences Required for Cell-Specific Gene Expression and Autoregulation in the Inner Ear and Central Nervous System Mol. Cell. Biol., March 15, 2008; 28(6): 1905 - 1914. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. T. Schwartz and H. R. Horvitz The C. elegans protein CEH-30 protects male-specific neurons from apoptosis independently of the Bcl-2 homolog CED-9 Genes & Dev., December 1, 2007; 21(23): 3181 - 3194. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Kawauchi, H. Taniguchi, H. Watanabe, T. Saito, and F. Murakami Direct visualization of nucleogenesis by precerebellar neurons: involvement of ventricle-directed, radial fibre-associated migration. Development, March 1, 2006; 133(6): 1113 - 1123. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Ovcharenko and M. A. Nobrega Identifying synonymous regulatory elements in vertebrate genomes Nucleic Acids Res., July 1, 2005; 33(suppl_2): W403 - W407. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Offner, N. Duval, M. Jamrich, and B. Durand The pro-apoptotic activity of a vertebrate Bar-like homeobox gene plays a key role in patterning the Xenopus neural plate by limiting the number of chordin- and shh-expressing cells Development, April 15, 2005; 132(8): 1807 - 1818. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Alfano, C. Vitiello, C. Caccioppoli, T. Caramico, A. Carola, M. J. Szego, R. R. McInnes, A. Auricchio, and S. Banfi Natural antisense transcripts associated with genes involved in eye development Hum. Mol. Genet., April 1, 2005; 14(7): 913 - 923. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. E. Olson, J. Zhang, H. Taylor, D. W. Rose, and M. G. Rosenfeld Barx2 functions through distinct corepressor classes to regulate hair follicle remodeling PNAS, March 8, 2005; 102(10): 3708 - 3713. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Lim and K.-W. Choi Induction and autoregulation of the anti-proneural gene Bar during retinal neurogenesis in Drosophila Development, November 15, 2004; 131(22): 5573 - 5580. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Poggi, T. Vottari, G. Barsacchi, J. Wittbrodt, and R. Vignali The homeobox gene Xbh1 cooperates with proneural genes to specify ganglion cell fate within the Xenopus neural retina Development, May 15, 2004; 131(10): 2305 - 2315. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Mo, S. Li, X. Yang, and M. Xiang Role of the Barhl2 homeobox gene in the specification of glycinergic amacrine cells Development, April 1, 2004; 131(7): 1607 - 1618. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Li, F. Qiu, A. Xu, S. M. Price, and M. Xiang Barhl1 Regulates Migration and Survival of Cerebellar Granule Cells by Controlling Expression of the Neurotrophin-3 Gene J. Neurosci., March 24, 2004; 24(12): 3104 - 3114. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Lim and K.-W. Choi Bar homeodomain proteins are anti-proneural in the Drosophila eye: transcriptional repression of atonal by Bar prevents ectopic retinal neurogenesis Development, December 15, 2003; 130(24): 5965 - 5974. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. DeMyer, A. Espay, L. Walsh, S. Benes, and M. Edwards-Brown Vermian Hypoplasia and Arrested Cerebral Myelination in Two Sisters: Variant of Joubert's Syndrome or a New Syndrome? J Child Neurol, November 1, 2003; 18(11): 755 - 762. [Abstract] [PDF] |
||||
![]() |
R. Saba, N. Nakatsuji, and T. Saito Mammalian BarH1 Confers Commissural Neuron Identity on Dorsal Cells in the Spinal Cord J. Neurosci., March 15, 2003; 23(6): 1987 - 1991. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Li, S. M. Price, H. Cahill, D. K. Ryugo, M. M. Shen, and M. Xiang Hearing loss caused by progressive degeneration of cochlear hair cells in mice deficient for the Barhl1 homeobox gene Development, March 9, 2003; 129(14): 3523 - 3532. [Abstract] [Full Text] [PDF] |
||||







