Proteomic analyses of nucleus laminaris identified candidate targets of the fragile X mental retardation protein

被引:7
作者
Sakano, Hitomi [1 ]
Zorio, Diego A. R. [2 ]
Wang, Xiaoyu [2 ]
Ting, Ying S. [3 ]
Noble, William S. [3 ]
MacCoss, Michael J. [3 ]
Rubel, Edwin W. [1 ]
Wang, Yuan [2 ,4 ]
机构
[1] Univ Washington, Dept Otolaryngol Head & Neck Surg, Sch Med, Virginia Merrill Bloedel Hearing Res Ctr, Seattle, WA 98195 USA
[2] Florida State Univ, Dept Biomed Sci, 1115 West Call St, Tallahassee, FL 32306 USA
[3] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
[4] Florida State Univ, Program Neurosci, Tallahassee, FL 32306 USA
关键词
autism spectrum disorders; cytoskeletal proteins; dendritic plasticity; gene ontology; RNA binding protein; RhoC; RRID: AB_94856; RRID: AB_776174; RRID: AB_297884; RRID: AB_357520; RRID: AB_309663; RRID: AB_2277755; RRID: AB_2155806; RRID: AB_1859928; RRID: AB_10615780; RRID: AB_2620155; ACTIVITY-DEPENDENT REGULATION; STEM AUDITORY NUCLEI; MESSENGER-RNA; MOLECULAR-MECHANISMS; AFFERENT INFLUENCES; MOUSE MODEL; FMRP; CHICK; LOCALIZATION; TRANSLATION;
D O I
10.1002/cne.24281
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The avian nucleus laminaris (NL) is a brainstem nucleus necessary for binaural processing, analogous in structure and function to the mammalian medial superior olive. In chickens (Gallus gallus), NL is a well-studied model system for activity-dependent neural plasticity. Its neurons have bipolar extension of dendrites, which receive segregated inputs from two ears and display rapid and compartment-specific reorganization in response to unilateral changes in auditory input. More recently, fragile X mental retardation protein (FMRP), an RNA-binding protein that regulates local protein translation, has been shown to be enriched in NL dendrites, suggesting its potential role in the structural dynamics of these dendrites. To explore the molecular role of FMRP in this nucleus, we performed proteomic analysis of NL, using micro laser capture and liquid chromatography tandem mass spectrometry. We identified 657 proteins, greatly represented in pathways involved in mitochondria, translation and metabolism, consistent with high levels of activity of NL neurons. Of these, 94 are potential FMRP targets, by comparative analysis with previously proposed FMRP targets in mammals. These proteins are enriched in pathways involved in cellular growth, cellular trafficking and transmembrane transport. Immunocytochemistry verified the dendritic localization of several proteins in NL. Furthermore, we confirmed the direct interaction of FMRP with one candidate, RhoC, by in vitro RNA binding assays. In summary, we provide a database of highly expressed proteins in NL and in particular a list of potential FMRP targets, with the goal of facilitating molecular characterization of FMRP signaling in future studies.
引用
收藏
页码:3341 / 3359
页数:19
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