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Patterns of gene expression associated with Pten deficiency in the developing inner ear
- 작성일2018-02-05
- 최종수정일2018-02-05
- 담당부서연구기획과
- 연락처043-719-8033
- 1,915
PLOS one, 2014, 01, e97544-1─e97544-9
Patterns of gene expression associated with Pten deficiency in the developing inner ear
Hyung Jin Kim, J Ryu, H Woo, S Kim, M Park, S Koo
Abstract
In inner ear development, phosphatase and tensin homolog (PTEN) is necessary for neuronal maintenance, such as neuronal survival and accurate nerve innervations of hair cells. We previously reported that Pten conditional knockout (cKO) mice exhibited disorganized fasciculus with neuronal apoptosis in spiral ganglion neurons (SGNs). To better understand the genes and signaling networks related to auditory neuron maintenance, we compared the profiles of differentially expressed genes (DEGs) using microarray analysis of the inner ear in E14.5 Pten cKO and wild-type mice. We identified 46 statistically significant trans using significance analysis of microarrays, with the false-discovery rate set at 0%. Among the DEGs, expression levels of candidate genes and expression domains were validated by quantitative real-time RT-PCR and in situ hybridization, respectively. Ingenuity pathway analysis using DEGs identified significant signaling networks associated with apoptosis, cellular movement, and axon guidance (i.e., secreted phosphoprotein 1 (Spp1)-mediated cellular movement and regulator of G-protein signaling 4 (Rgs4)-mediated axon guidance). This result was consistent with the phenotypic defects of SGNs in Pten cKO mice (e.g., neuronal apoptosis, abnormal migration, and irregular nerve fiber patterns of SGNs). From this study, we suggest two key regulatory signaling networks mediated by Spp1 and Rgs4, which may play potential roles in neuronal differentiation of developing auditory neurons.
- ISBN or ISSN: 1932-6203
- 본 연구는 질병관리본부 연구개발과제(과제번호 2012-NG61002-00) 연구비를 지원받아 수행되었습니다.
- This research was supported by a fund(code 2012-NG61002-00) by Research of Korea Centers for Disease Control and Prevention.
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