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2022 Fiscal Year Final Research Report

A constructive approach for duplex vision using mathematical and mouse models.

Research Project

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Project/Area Number 20K06737
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 44050:Animal physiological chemistry, physiology and behavioral biology-related
Research InstitutionUniversity of Tsukuba

Principal Investigator

Sakurai Keisuke  筑波大学, 生命環境系, 助教 (20647317)

Project Period (FY) 2020-04-01 – 2023-03-31
Keywords視細胞 / 網膜 / オプシン / 小口病 / ノックインマウス
Outline of Final Research Achievements

In vertebrate retina, rod and cone photoreceptors are responsible for scotopic and photopic vision, respectively. The light sensitivity and kinetics of the photoreceptors differ depending on their vison. To elucidate the relationship between photoresponse properties and the phototransduction cascades in both photoreceptor cells, we created three mouse models of (1) cyclostome-type rhodopsin (2) rhodopsin-like cone opsin (3) cone-associated Oguchi disease. We found that the conserved residues in rhodopsin group were involved in the light sensitivity of rods, while the residue conserved in cone opsins were involved in the cone response kinetics. Also, we proposed a novel mechanism that causes the cone-associated Oguchi disease.

Free Research Field

動物生理学

Academic Significance and Societal Importance of the Research Achievements

これまで小口病のマウスモデルは、原因遺伝子ノックアウトマウスが用いられてきた。しかし、ノックアウトマウスは桿体の異常に関してはいいモデルであるが、ヒト錐体の光応答の回復に異常がみられる症例について説明できなかった。本研究において作出した錐体関連の小口病マウスモデルから、ヒト錐体の回復異常に発症に関する新規の機序を明らかにすることができた

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Published: 2024-01-30  

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