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2016 Fiscal Year Final Research Report

Development of a simple method to suppress the cleavage for the production of purely cultured cultivars - Elucidation of microtubule regeneration mechanism -

Research Project

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Project/Area Number 26450270
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Aquatic bioproduction science
Research InstitutionKindai University

Principal Investigator

KOBAYASHI Toru  近畿大学, 農学部, 教授 (00298944)

Research Collaborator FUJII Hikaru  
YAMAZAKI Keiya  
INOKUMA Toru  
OHASHI Shota  
Project Period (FY) 2014-04-01 – 2017-03-31
Keywords卵割阻止 / 高温刺激 / 四倍体 / 倍数化 / 単極紡錘体 / 中心小体 / 完全同型接合体 / クローン
Outline of Final Research Achievements

Conditions for the efficient suppression of the cleavage of fertilized eggs of honmoroko by multiple times of heat shock treatment (HST) and the cytological mechanism of the polyploidization by this manipulation was elucidated. In order to prevent cleavage of normally fertilized eggs cultured at 20°C by HST at 40.5°C for 1 minute (min), it was found that the first treatment should be conducted 25 min after the fertilization (the prophase of the first cleavage), and that second treatment should be conducted 15 min after the end of the first treatment. Then polyploidization will be done successfully with high frequency (46% of hatched larvae). Under this treatment condition, it was revealed that the first cleavage was prevented with formation of a monopolar spindle at the first cell cycle immediately after the second treatment, and the daughter chromosomes could not be separated, and gathers to one pole.

Free Research Field

魚類の育種学、細胞工学

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Published: 2018-03-22  

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