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Functional conservation of <i>atonal</i> and <i>Math1</i> in the CNS and PNS

DevelopmentPublished 1 March 2000
Nissim Ben‐Arie, Bassem A. Hassan, Nessan Bermingham, Denise Malicki, Dawna L. Armstrong, Martin M. Matzuk
Citations252
SJR quartileQ1
SJR score1.72
SNIP0.98

TL;DR

The insertion of (beta)-galactosidase into the Math1 locus and analysis of its expression demonstrated that both the mouse and fly homologs encode lineage identity information and some of the cells dependent on this information serve similar mechanoreceptor functions.

Abstract

To determine the extent to which atonal and its mouse homolog Math1 exhibit functional conservation, we inserted (beta)-galactosidase (lacZ) into the Math1 locus and analyzed its expression, evaluated consequences of loss of Math1 function, and expressed Math1 in atonal mutant flies. lacZ under the control of Math1 regulatory elements duplicated the previously known expression pattern of Math1 in the CNS (i.e., the neural tube, dorsal spinal cord, brainstem, and cerebellar external granule neurons) but also revealed new sites of expression: PNS mechanoreceptors (inner ear hair cells and Merkel cells) and articular chondrocytes. Expressing Math1 induced ectopic chordotonal organs (CHOs) in wild-type flies and partially rescued CHO loss in atonal mutant embryos. These data demonstrate that both the mouse and fly homologs encode lineage identity information and, more interestingly, that some of the cells dependent on this information serve similar mechanoreceptor functions.

Keywords

NeuroscienceBiochemistry, Genetics and Molecular Biology