147
Views
15
CrossRef citations to date
0
Altmetric
Original Article

Analysis of gene expression profiles along the tonotopic map of mouse cochlea by cDNA microarrays

, , PhD , MD, &
Pages 12-17 | Received 25 Mar 2009, Published online: 20 Jul 2009
 

Abstract

Conclusion: This study demonstrated differential gene expression profiles along the axis of the mouse cochlea. It also suggests the mechanism that establishes the tonotopic organization. Objectives: The molecular basis of the tonotopic mapping of the mammalian cochlea remains unclear. We therefore examined the genes that were abundantly expressed in either the apex or the base of mouse cochlea. Materials and methods: Apical and basal portions of cochlea, which contained the organ of Corti and spiral ganglion neurons, were independently dissected from 10 adult C57BL/6 mice, and their total RNAs were respectively isolated. The gene expression profiles of each of these two pools were examined and compared to each other by the complementary DNA microarray technique. Results: Of 20 289 probes tested, 64 genes were found to be expressed in the apical portion more than fivefold more abundantly than in the basal portion, and 77 genes were vice versa. Of interest, the genes of several functional proteins such as β2- and γ2-subunits of GABAA receptors dominated the basal part, indicating that these molecules may be involved in high-frequency tuning of the hair cells and/or ganglion neurons.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.