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2017 Fiscal Year Final Research Report

The role of Sip1 gene for development of the serotonergic neurons of the raphe

Research Project

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Project/Area Number 26461557
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Pediatrics
Research InstitutionYokohama College of Pharmacy (2017)
Institute for Developmental Research, Aichi Human Service Center (2014-2015)

Principal Investigator

NISHIZAKI Yuriko  横浜薬科大学, 薬学部, 講師 (90378901)

Co-Investigator(Kenkyū-buntansha) 東 雄二郎  愛知県心身障害者コロニー発達障害研究所, 周生期学部, 部長 (30181069)
Project Period (FY) 2014-04-01 – 2017-03-31
Keywords縫線核 / セロトニン / 神経 / Sip1 / 脳 / ノックアウトマウス
Outline of Final Research Achievements

Sip1 is the causative gene for Mowat-Wilson syndrome. Sip1 is expressed in the developing neural tube, the neural crest cells, the hippocampus and the cerebral cortex. Sip1 is also expressed in the serotonergic neurons of the raphe nuclei in the brainstem. Serotonergic neurons of the raphe nuclei project throughout the brain widely and secret serotonin. Serotonin acts as key modulator of neural circuits for emotion, mood and physiological response. We generated Sip1-gene conditional knockout mice in the serotonin neurons of the Raphe. We observed abnormal behavior of the Sip1 conditional knockout mice and some abnormal morphology of the serotonergic neurons. The results suggest that Sip1 gene play an important role for serotonergic neuron development and function.

Free Research Field

器官発生学、分子生物学、神経科学

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Published: 2019-03-29  

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