Evolutionary conservation of sequence and expression of the bHLH protein Atonal suggests a conserved role in neurogenesis

Nissim Ben-Arie, Alanna E. McCall, Scott Berkman, Gregor Eichele, Hugo J. Bellen, Huda Y. Zoghbi*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

140 Scopus citations


atonal is a Drosophila proneural gene that belongs to the family of basic helix-loop-helix (bHLH)-containing proteins. It is expressed in the chordotonal organs and photoreceptor cells, and flies that lack Atonal protein are ataxic and blind. Here we report the cloning of atonal homologs from red flour beetle, puffer fish, chicken, mouse, and human. The bHLH domain is conserved throughout evolution, while the entire coding region is highly similar in mammals. Both the chicken and the mouse homologs are expressed early in embryogenesis in the hind brain, and specifically in cells predicted to give rise to the external granular layer of the cerebellum. In addition, these genes are expressed throughout the dorsal part of the spinal cord, in patterns different from those found for other genes, like LH-2 and wnt-1. The mouse homolog (Math1) maps to mouse chromosome 6, and the human homolog (NATH1) to human chromosome 4q22. Two neurological mouse mutants, Lc and chp, were found to map to the vicinity of Math1, but are not caused by mutations in Math1. The evolutionary conservation of this gene and its mRNA expression patterns during embryogenesis suggests that it plays a key role in the development of the vertebrate central nervous system.

Original languageAmerican English
Pages (from-to)1207-1216
Number of pages10
JournalHuman Molecular Genetics
Issue number9
StatePublished - Sep 1996
Externally publishedYes

Bibliographical note

Funding Information:
We thank the YAC core, headed by Dr Craig Chinault, and the FISH core, headed by Dr Antonio Baldini, both at the Genome Center at Baylor College of Medicine, for the screening of the YAC library and FISH mapping, respectively. We are grateful to Dr Eva Eicher for the generous gift of backcross DNA panels, assistance in analysis of the mouse mapping data and for critical review of the manuscript. We would like to thank Dr Muriel Davisson for providing chp DNA and sharing unpublished information, Dr Achim Gossler for providing the Etl1 probe, Dr Nathaniel Heintz for sharing unpublished mouse mapping data, Dr Igna Van den Veyver for comments on the manuscript, and Catherine Tasnier for catalyzing this fruitful collaboration. H.Y.Z. is an Investigator and H.J.B. is an Associate Investigator from the Howard Hughes Medical Institute. This work was supported by a grant from the National Institutes of Health, National Institute of Neurological Disease and Stroke (NS27699) to H.Y.Z.


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