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2014 Fiscal Year Final Research Report

Retinal phosphoprotein analysis in novel Src mutant optic neuropathy mouse model

Research Project

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Project/Area Number 25670729
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Ophthalmology
Research InstitutionUniversity of Yamanashi

Principal Investigator

KATO Goro  山梨大学, 総合研究部, 助教 (60177441)

Project Period (FY) 2013-04-01 – 2015-03-31
Keywords網膜 / Src / リン酸化タンパク質
Outline of Final Research Achievements

Degradation of activated Src is regulated by Cdk5-dependent phosphorylation of Src Ser75. RGC loss was stimulated without elevated intraocular pressure in the aged phospho-mimicking mutant SrcSer75Asp mice (SD mice).To address the molecular mechanism of the degeneration induced by deregulation of the Ser75 phosphorylation, we established 2-D Fluorescence Difference Gel Electrophoresis (2-D DIGE) to globally detect changes in the retinal phosphoprotein abundance in retinas. The level of spot #30, which had an apparent molecular weight of 45kDa and an isoelectric point of 5.5~6.5, in SD mice was increased significantly than that of wild type mice.These results can lead to identification of retinal phosphoproteins changed by the Src-specific phosphorylation mutation, and are very important in elucidating the mechanism of RGC degeneration.

Free Research Field

分子細胞生物学

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Published: 2016-06-03  

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